Sabtu, 10 Juli 2010

MACAM-MACAM MEDIA PRODUCT PHYTOTECH

ANDERSON BASAL SALT MIXTURE

ANDERSON BASAL SALT MIXTURE
Product ID: A267

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY ANDERSON (1978, 1980)
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

A267 Anderson Basal Salt Mixture

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 1.89 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Anderson (1978,
1980)
pH = 3.25 – 4.25

Application Notes
Plant Tissue Culture Tested
Plant Species: Rhododendron, Rubus (red and black raspberry).
Anderson achieved a two-fold increase in multiplication of red raspberries using this formulation
compared to MS. The optimal concentrations of growth regulators for shoot multiplication of red
and black raspberries was 0.1 – 2.5 μM IBA and 4.5 – 9.0 μM BA.
Anderson’s medium contains approximately ¼ strength NH4NO3 and KNO3 compared to MS.
References
Anderson, WC. 1978. Tissue culture propagation of Rhododendrons. In Vitro 14: 334.
Anderson, WC. 1980. Tissue culture propagation of red and black raspberries ,Rubus idaeus
and R. occidentalis . Acta Hort. 112: 13-20.


BANANA AGS BASAL MEDIUM

BANANA AGS BASAL MEDIUM
Product ID: B144

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, VITAMINS, AND PLANT GROWTH REGULATORS REQUIRED TO CULTURE BANANAS.
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36



CAPE SUNDEW/ VENUS FLYTRAP MULTIPLICATION BASAL MEDIUM

CAPE SUNDEW/ VENUS FLYTRAP MULTIPLICATION BASAL MEDIUM
Product ID: C206

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- & MICRONUTRIENTS, VITAMINS, & PGR'S REQUIRED FOR CARNIVOROUS PLANTS.
PLANT TISSUE CULTURE TESTED

C206
Cape Sundew/ Venus Flytrap Multiplication Basal Medium
Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Plant Tissue Culture
Solubility:
Water
Typical Working Concentration:
2.12 g/L
Storage Temp:
2 – 6° C
Storage Temp of Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes:
Contains the macro- and micronutrients, vitamins, and plant growth regulators required to stimulate multiplication in cultures of Cape Sundew and Venus Flytrap.
Typical (unadjusted ) pH = 3.0 – 4.0; see certificate of analysis for lot-specific value. Adjust pH to desired level during medium preparation.


Application Notes
Plant Tissue Culture Tested
Plant Species: Cape Sundew (Drosera capensis), Venus Flytrap (Dionaea muscipula)
Revised 3/2010

CARNIVOROUS PLANT (NEPENTHES) BASAL SALT MIXTURE

CARNIVOROUS PLANT (NEPENTHES) BASAL SALT MIXTURE
Product ID: C1935

Storage Temperature: 2 to 6 C

Description: CARNIVOROUS PLANT (NEPENTHES) BASAL SALT MIXTURE

PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36


C1935
Carnivorous Plant (Nepenthes) Basal Salt Mixture
Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Carnivorous Plant Culture
Solubility:
Soluble in Water
Typical Working Concentration:
0.65 g/L
Storage Temp:
2 - 6° C
Storage Temp of Stock Solution:
Preparation of concentrated stock solution is not recommended as insoluble precipitates may form.
Other Notes:
Does not contain sucrose, plant growth regulators, or gelling agent.


Application Notes
Plant Tissue Culture Tested
Plant Species: Carnivorous Plants
This medium is commonly supplemented with MS Vitamins (e.g., M533, M553) and 25 g/L sucrose.
References
R. de Fossard. Posted on the Plant TC Listserv, Sept. 2009. Subject: Nepenthes diatas. (http://lists.umn.edu/cgi-bin/wa?A2=ind0901&L=PLANT-TC&T=0&F=&S=&X=1050D3258E48269160&P=2728). Also posted on: http://www.labflytrap.com/forum/viewtopic.php?f=7&t=209&start=0.


CARROT CALLUS INTIATION MEDIUM FROM PITH TISSUE.

CARROT CALLUS INTIATION MEDIUM FROM PITH TISSUE.
Product ID: C212

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, VITAMINS, & PLANT GROWTH REGULATORS REQUIRED TO INITIATE CARROT CALLUS
PLANT TISSUE CULTURE TESTED

C212
Carrot Callus Initiation
Basal Medium
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.21 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients, vitamins, and plant growth
regulators required to initiate carrot callus from root tissue.
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture Tested
Plant species: Carrot (Daucus carota )
References

Establishment and Maintenance of Carrot Callus
Carrot [Daucus carota L. subsp. Sativus (Hoffm.)] is a cool season plant grown for its edible storage taproot. Since the discovery of somatic embryogenesis in carrot culture was made by Steward and Reinert, it has become a model system for investigating many biochemical, physiological, and genetic aspects of plant cell culture. This procedure will outline the method for establishing carrot callus cultures.
Materials Required
1. 10 glass or plastic petri dishes (100 mm in diameter)
2. 2 pairs of forceps and 2 scalpels
3. Sterile #2 cork borer and glass rod that fits it
4. 1000-ml beaker and 250-ml beaker
5. Waterproof marking pen and labels
6. 4 plastic slant racks to hold solid culture tubes
7. Analytical balance
8. Bunsen or ethanol burner
9. 500 ml of 20% Clorox solution supplemented with a few drops of Tween-20
10. 500 ml of sterile distilled water
11. 200 ml of 95% ethanol
12. Carrot Callus Initiation Medium, Product Number C212
13. Carrot Shoot Development Medium, Product Number C222
14. 1 or 2 healthy, undamaged, and regularly shaped carrot roots.

Procedures
1. Wipe down and turn on laminar flow hood 15 min before doing any work in the hood. Flame-sterilize instruments.
2. Clean carrot root by scrubbing under running tap water to remove any surface soil. Trim the carrot into 100-mm sections and place them in a 1000-ml beaker. Cover with 20% Clorox solution for approximately 20 min and then decant the Clorox solution. Rinse the explant three times in sterile distilled water covering the tissue with each rinse.
3. While carrot sections are being sterilized, prepare and dispense media into culture vessels according to protocols in the media preparation section. Place the culture vessels in racks and label them with respective treatments, medium, and date.
4. Transfer sterilized carrot slices to a sterile petri dish. Using a sterile cork borer, punch out 8-10 cylinders of tissue from the secondary phloem cambial region of the carrot slices. Do not punch out more than two cylinders of tissue at one time, as you may have difficulty in removing them from the cork borer. Using a sterile glass rod, push the cylinders from the cork borer into a sterile petri dish. Using a sharp, sterile scalpel, remove the ends of the tissue cylinder. Next cut the remaining portion of the cylinder into 2- to 3-mm-thick sections. Using a sterile petri plate on the balance, weigh each explant section individually and inoculate into the culture vessels containing the Carrot Callus Initiation Medium, placing one explant per tube. Repeat this procedure until all culture vessels containing the Carrot Callus Initiation medium have been inoculated. Use a different forcep for each explant and flame the forceps between transfers. Flame the lid of the culture tubes immediately after opening and before closing.
Callus should be removed from the primary explant after 45 days. The calli can be subcultured onto the same medium for further callus growth or it can be subcultured onto the Carrot Shoot Development medium for shoot initiation.



CARROT SHOOT DEVELOPMENT BASAL MEDIUM

CARROT SHOOT DEVELOPMENT BASAL MEDIUM
Product ID: C222

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, VITAMINS, AND PGR'S REQUIRED TO INITIATE SHOOTS FROM CARROT CALLUS.
PLANT TISSUE CULTURE TESTED

C222 Carrot Shoot Development Basal Medium
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.21 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients, vitamins, and plant growth
regulators required to initiate shoots from carrot callus.
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture Tested
Plant species: Carrot (Daucus carota )
References

CHEE & POOL C2d VITIS BASAL MEDIUM

CHEE & POOL C2d VITIS BASAL MEDIUM
Product ID: C287

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY CHEE & POOL (1987).
PLANT TISSUE CULTURE TESTED

C287
Chee & Pool C2d Vitis
Basal Medium
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 4.49 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients and vitamins as described by Chee
and Pool (1987).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture Tested
Plant Species: Grape (Vitis spp)
This medium was developed to improve grape shoot multiplication. This formulation has
reduced levels of chloride, Iodide, and manganese compared to MS. Calcium chloride was
replaced by calcium nitrate, thus improving the quality of grave shoots.
References
Chee, R and RM Pool. 1987. Improved inorganic media constituents for in vitro shoot
multiplication of Vitis. Sci. Hort. 32: 85.

CHU N6 VITAMIN SOLUTION (1000x)

CHU N6 VITAMIN SOLUTION (1000x)
Product ID: C149

Storage Temperature: 2 to 6 C

Description: CONTAINS THE VITAMINS DESCRIBED BY CHU (1975).USE AT A CONCENTRATION OF 1 mL/L OF MEDIUM TO ACHIEVE PROPER FINAL CONCENTRATION.
PLANT TISSUE CULTURE TESTED

C149
Chu N6 Vitamin Solution (1000x)
Properties
Form: Liquid
Appearance: Clear, Colorless Solution
Application: Plant Tissue Culture
Solubility: Miscible with Water
Typical Working
Concentration: 1.0 mL/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution: N/A
Other Notes: Contains the vitamins as described by Chu et al. (1975).
pH = 3.75 – 4.75



Application Notes
Plant Tissue Culture Tested
References
Chu CC, CC Wang, CS Sun, C Hsu, KC Yin, CY Chu and FY Bi. (1975) Scientia Sinic. 18: 659-
668.

CHU'S N6 BASAL MEDIUM w/ VITAMINS

CHU'S N6 BASAL MEDIUM w/ VITAMINS
Product ID: C167

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, AND VITAMINS AS DESCRIBED BY CHU (1975).
PLANT TISSUE CULTURE TESTED

C167
Chu N6 Basal Medium
w/ Vitamins

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.99 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients and vitamins as described by Chu
et al. (1975).
pH = 3.5 – 4.5


Application Notes
Plant Tissue Culture Tested
Plant species: rice (Oryza sativa )
Chu (N6) Medium was developed to promote the initiation, growth, and differentiation of callus
from rice pollen cultures.
Ammonium nitrate has been replaced by ammonium sulfate. The molar concentration of NH4
+
is 7.0 mM compared to 20.6mM for MS.
References
Chu CC, CC Wang, CS Sun, C Hsu, KC Yin, CY Chu and FY Bi. (1975) Scientia Sinic. 18: 659-
668.

CHU'S N6 BASAL SALT MIXTURE

CHU'S N6 BASAL SALT MIXTURE
Product ID: C416

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY CHU (1975).
PLANT TISSUE CULTURE TESTED

C416
Chu N6 Basal Salt Mixture

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.98 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Chu et al. (1975).
pH = 3.75 – 4.75

Application Notes
Plant Tissue Culture Tested
Plant species: rice (Oryza sativa )
Chu (N6) Medium was developed to promote the initiation, growth, and differentiation of callus
from rice pollen cultures.
Ammonium nitrate has been replaced by ammonium sulfate. The molar concentration of NH4
+
is 7.0 mM compared to 20.6mM for MS.
References
Chu CC, CC Wang, CS Sun, C Hsu, KC Yin, CY Chu and FY Bi. (1975) Scientia Sinic. 18: 659-
668.

DCR BASAL SALT MIXTURE

DCR BASAL SALT MIXTURE
Product ID: D146

Storage Temperature: 2 to 6 C

Description: CONTAINS MACRO- AND MICRONUTRIENTS AS DESCRIBED BY GUPTA & DURZAN (1985).
PLANT TISSUE CULTURE TESTED

TARIFF CODE: 3105.90.0000

RISK & SAFETY: R: 8/36/37/38 S: 17/26/36

D146
DCR Basal Salt Mixture

Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Plant Tissue Culture
Solubility:
Water
Typical Working Concentration:
1.64 g/L
Storage Temp:
2 – 6° C
Storage Temp of Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes:
Contains the macro- and micronutrients as described by Gupta and Durzan. (1985).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture Tested
Plant Species: Douglas Fir (Pseudotsuga spp.) and Sugar Pine (Pinus lambertiana)
This medium was developed to promote shoot proliferation. This formulation has approximately ¼ the concentration of NH4NO3 and KNO3 compared to MS. Additional Ca+2 and NO3- ions are supplied by Ca(NO3)2.
References
Gupta, PK and KJ Durzan. 1985. Shoot multiplication from mature Douglas-fir and sugar pine. Plant Cell Reports 4:177-179.

DKW BASAL MEDIUM, CONTAINS 10 g/L SUCROSE

DKW BASAL MEDIUM, CONTAINS 10 g/L SUCROSE
Product ID: D191

Storage Temperature: 2 to 6 C

Description: W/O VITAMINS, CONTAINS MACRO- AND MICRONUTRIENTS AS DESCRIBED BY DRIVER & KUNIYUKI (1984) AND MCGRANAHAN ET AL. (1987).

The high calcium level in this medium may inhibit many gellan gums from completely melting during autoclaving. For this reason the use of Gellan Gum with this medium is not recommended as a clear, firm gel may not be obtained.

PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 36/37/38 S: 26/36

D191
DKW Basal Medium
Synonym:
DKW Basal Salts w/ Sucrose
Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Plant Tissue Culture
Solubility:
Water
Typical Working Concentration:
15.22 g/L
Storage Temp:
2 – 6° C
Storage Temp of Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes:
Contains the macro- and micronutrients as described by Driver and Kuniyuki (1984) and McGranahan, et al. (1987).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture Tested. Plant species: Northern California Walnut (Juglans hindsii)
This medium was developed for the multiplication of shoots from nodal explants. The medium was supplemented with 4.5 μM BA and 5 nM IBA. Rooting the shoots was enhanced by dipping the basal ends of the shoots in 5 mM IBA prior to transferring to the greenhouse.
References
Driver, JA and AH Kuniyuki. 1984. HortSci 19:507-509.
McGranahan, GH, et al. 1987. In: Bonga, JB and DJ Durzan, Editors, Cell and Tissue Culture in Forestry. Martinus Nijhoff, Dordrecht, pp 261-271.

DKW BASAL MEDIUM, CONTAINS 30 G/L SUCROSE.

DKW BASAL MEDIUM, CONTAINS 30 G/L SUCROSE.
Product ID: D189

Storage Temperature: 2 to 6 C

Description: W/OUT VITAMINS; CONTAINS MACRO- AND MICRONUTRIENTS AS DESCRIBED BY DRIVER & KUNIYUKI (1984) AND MCGRANAHAN, et al. (1987)

The high calcium level in this medium may inhibit many gellan gums from completely melting during autoclaving. For this reason the use of Gellan Gum with this medium is not recommended as a clear, firm gel may not be obtained.

PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 36/37/38 S: 26/36

D189
DKW Basal Medium
Synonym:
DKW Basal Salts w/ Sucrose

Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Plant Tissue Culture
Solubility:
Water
Typical Working Concentration:
35.22 g/L
Storage Temp:
2 – 6° C
Storage Temp of Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes:
Contains the macro- and micronutrients as described by Driver and Kuniyuki (1984) and McGranahan, et al. (1987).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture
Plant species: Northern California Walnut (Juglans hindsii)
This medium was developed for the multiplication of shoots from nodal explants. The medium was supplemented with 4.5 μM BA and 5 nM IBA. Rooting the shoots was enhanced by dipping the basal ends of the shoots in 5 mM IBA prior to transferring to the greenhouse.
References
Driver, JA and AH Kuniyuki. 1984. HortSci 19:507-509.
McGranahan, GH, et al. 1987. In: Bonga, JB and DJ Durzan, Editors, Cell and Tissue Culture in Forestry. Martinus Nijhoff, Dordrecht, pp 261-271.

DKW BASAL SALT MIXTURE

DKW BASAL SALT MIXTURE
Product ID: D190

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY DRIVER & KUNIYUKI (1984) AND MCGRANAHAN, ET AL (1987).

The high calcium level in this medium may inhibit many gellan gums from completely melting during autoclaving. For this reason the use of Gellan Gum with this medium is not recommended as a clear, firm gel may not be obtained.

PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8/36/37/38 S: 17/26/36

D190
DKW Basal Salt Mixture
Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Plant Tissue Culture
Solubility:
Water
Typical Working Concentration:
5.22 g/L
Storage Temp:
2 – 6° C
Storage Temp of Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes:
Contains the macro- and micronutrients as described by Driver and Kuniyuki (1984) and McGranahan, et al. (1987).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture
Plant species: Northern California Walnut (Juglans hindsii)
This medium was developed for the multiplication of shoots from nodal explants. The medium was supplemented with 4.5 μM BA and 5 nM IBA. Rooting the shoots was enhanced by dipping the basal ends of the shoots in 5 mM IBA prior to transferring to the greenhouse.
References
Driver, JA and AH Kuniyuki. 1984. HortSci 19:507-509.
McGranahan, GH, et al. 1987. In: Bonga, JB and DJ Durzan, Editors, Cell and Tissue Culture in Forestry. Martinus Nijhoff, Dordrecht, pp 261-271.

DKW MEDIUM W/ VITAMINS

DKW MEDIUM W/ VITAMINS
Product ID: D2470

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO-, MICRONUTRIENTS, AND VITAMINS AS DESCRIBED BY DRIVER & KUNIYUKI (1984) AND MCGRANAHAN, ET AL (1987).

The high calcium level in this medium may inhibit many gellan gums from completely melting during autoclaving. For this reason the use of Gellan Gum with this medium is not recommended as a clear, firm gel may not be obtained.

PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8/36/37/38 S: 17/26/36

D2470
DKW Basal Medium with Vitamins
Properties
Form:
Powder
Appearance:
White to Yellow Powder
Application:
Plant Tissue Culture
Solubility:
Water
Typical Working Concentration:
5.32 g/L
Storage Temp:
2 – 6° C
Storage Temp of Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes:
Contains the macro- and micronutrients and vitamins as described by Driver and Kuniyuki (1984) and corrected by McGranahan, et al. (1987).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture
Plant species: Northern California Walnut (Juglans hindsii)
This medium was developed for the multiplication of shoots from nodal explants. The medium was supplemented with 4.5 μM BA and 5 nM IBA. Rooting the shoots was enhanced by dipping the basal ends of the shoots in 5 mM IBA prior to transferring to the greenhouse.
References
Driver, JA and AH Kuniyuki. 1984. HortSci 19:507-509.
McGranahan, GH, et al. 1962. In: Bonga, JB and DJ Durzan, Editors, Cell and Tissue Culture in Forestry. Martinus Nijhoff, Dordrecht, pp 261-271.

ECONOMOU & READ BASAL MEDIUM
Product ID: E575

Storage Temperature: 2 to 6 C

Description:
Contains the macro- and micronutrients and vitamins as described by Economou & Read (1984)
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

ERIKSSON VITAMIN SOLUTION (1000x)

ERIKSSON VITAMIN SOLUTION (1000x)
Product ID: E330

Storage Temperature: 2 to 6 C

Description: CONTAINS THE VITAMINS DESCRIBED BY ERIKSON(1965).
USE A CONCENTRATION OF 1mL/L OF MEDIUM TO ACHIEVE PROPER FINAL CONCENTRATION
PLANT TISSUE CULTURE TESTED
STERILE

E330
Eriksson Vitamin Solution (1000x)

Properties
Form: Liquid
Appearance: Clear, Colorless Solution
Application: Plant Tissue Culture
Solubility: Miscible with Water
Typical Working
Concentration: 1.0 mL/L of Medium
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution: N/A
Other Notes: Contains the vitamins as described by Eriksson (1965).
pH = 3.75 – 4.75



Application Notes
Plant Tissue Culture Tested
References
Eriksson, T. 1965. Physiol. Plant 18:976-993.

EXS IIIa™ BASAL SALT MEDIUM WITH ADENINE

EXS IIIa™ BASAL SALT MEDIUM WITH ADENINE
Product ID: E333

Storage Temperature: 2 to 6 C

Description:
EXS IIIa™ is a proprietary plant cell culture medium that was originally developed for the culture of foliage plants such as Syngonium, Ficus, and Spathiphyllum.
PLANT TISSUE CULTURE TESTED

E333
EXS IIIa™ BASAL MEDIUM
Contains Adenine Hemisulfate

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.95 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Proprietary Formula
Contains myo-Inositol and Thiamine HCl
Does not contain carbohydrates or gelling agents
Application Notes
Plant Tissue Culture Tested
EXS IIIa™ is a proprietary plant cell culture medium that was originally developed for the culture
of foliage plants such as Syngonium , Ficus, and Spathiphyllum .
EXS IIIa™ has slightly less nitrogen and potassium compared to MS Medium, but higher
concentrations of calcium and magnesium. The reduced levels of nitrogen plus increased levels
of calcium and magnesium help support more productive growth in a wider range of plant
species.
References


EXS III™ BASAL MEDIUM W/OUT ADENINE

EXS III™ BASAL MEDIUM W/OUT ADENINE
Product ID: E337

Storage Temperature: 2 to 6 C

Description:
EXS III™ is a proprietary plant cell culture medium that was originally developed for the culture of foliage plants such as Syngonium, Ficus, and Spathiphyllum.
PLANT TISSUE CULTURE TESTED

E337
EXS III™ BASAL MEDIUM
WITHOUT ADENINE HEMISULFATE

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.87 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Proprietary Formula
Contains myo-Inositol and Thiamine
Does not contain carbohydrates or gelling agents
pH = 4.25 – 5.25
Application Notes
Plant Tissue Culture Tested
EXS III™ is a proprietary plant cell culture medium that was originally developed for the culture
of foliage plants such as Syngonium , Ficus, and Spathiphyllum .
EXS III™ has slightly less nitrogen and potassium compared to MS Medium, but higher
concentrations of calcium and magnesium. The reduced levels of nitrogen plus increased levels
of calcium and magnesium help support more productive growth in a wider range of plant
species.
References

Rata PenuhGAMBORG (PRL-4-DM) LONG BASAL MEDIUM

GAMBORG (PRL-4-DM) LONG BASAL MEDIUM
Product ID: G359

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, AND VITAMINS AS DESCRIBED BY GAMBORG, ET AL. (1966).
PLANT TISSUE CULTURE TESTED

G359
Gamborg (PRL-4-DM) Long
Basal Medium
Synonym: Gamborg B-5 Long Basal Medium

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 2.64 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Gamborg (1966).

Application Notes
Plant Tissue Culture
References
Gamborg, OL, 1966. Aromatic metabolism in plants. II. Enzymes of the shikimate pathway in
suspension cultures of plant cells. Can. J. Biochem. 44: 791-799.

GAMBORG B-5 BASAL MEDIUM

GAMBORG B-5 BASAL MEDIUM
Product ID: G398

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, AND VITAMINS AS DESCRIBED BY GAMBORG, ET AL. (1968).
PLANT TISSUE CULTURE TESTED

G398
Gamborg B-5 Basal Medium
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.21 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients and vitamins as described by
Gamborg, et al (1968).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture
Plant Species: Soybean (Glycine max )
This medium was developed for the initiation and growth of soybean cell suspensions. This
medium contains no ammonium nitrate; it does contain ammonium sulfate and increased levels
of potassium nitrate. Concentrations of NH4
+ over 2 mM inhibited cell growth.
Thiamine, an essential vitamin, is at a concentration 10x that of Linsmaier & Skoog Medium.
References
Gamborg, OL, RA Miller, K Ojima. 1968. Nutrient Requirements of suspension cultures of
soybean root cells. Exp. Cell Research 50: 151-158.

GAMBORG BASAL SALT MIXTURE

GAMBORG BASAL SALT MIXTURE
Product ID: G768

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY GAMBORG, ET AL. (1968).
PLANT TISSUE CULTURE TESTED

G768
Gamborg B-5 Basal Salt Mixture
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.10 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Gamborg, et al
(1968).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture
Plant Species: Soybean (Glycine max )
This medium was developed for the initiation and growth of soybean cell suspensions. This
medium contains no ammonium nitrate; it does contain ammonium sulfate and increased levels
of potassium nitrate. Concentrations of NH4
+ over 2 mM inhibited cell growth.
References
Gamborg, OL, RA Miller, K Ojima. 1968. Nutrient Requirements of suspension cultures of
soybean root cells. Exp. Cell Research 50: 151-158.


GAMBORG VITAMIN POWDER (1000x)

GAMBORG VITAMIN POWDER (1000x)
Product ID: G249

Storage Temperature: 2 to 6 C

Description: CONTAINS THE VITAMINS AS DESCRIBED BY GAMBORG, ET AL. (1968).
PLANT TISSUE CULTURE TESTED

G249
Gamborg Vitamin Powder (1000x)

Properties
Form: Powder
Appearance: White to Off-white powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration:
11.20 g/ 100 mL
1.0 mL/L of medium when reconstituted to volume indicated on the label.
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution: 2 – 6° C
Other Notes: Contains the vitamins as described by Gamborg (1968).
Myo-Inositol may precipitate out of the prepared stock solution when cold;
warming with occasional agitation will redissolved the precipitated myo-
Inositol.

Application Notes
Plant Tissue Culture Tested
References
Gamborg, OL, RA Miller, K Ojima. 1968. Nutrient Requirements of suspension cultures of
soybean root cells. Exp. Cell Research 50: 151-158.

GAMBORG VITAMIN SOLUTION (1000x)

GAMBORG VITAMIN SOLUTION (1000x)
Product ID: G219

Storage Temperature: 2 to 6 C

Description: USE AT A CONCENTRATION OF 1 ML/L OF MEDIUM TO ACHIEVE THE PROPER FINAL CONCENTRATION

STERILE
PLANT TISSUE CULTURE TESTED

G219
Gamborg Vitamin Solution (1000x)
Properties
Form: Liquid
Appearance: Clear, Colorless Solution
Application: Plant Tissue Culture
Solubility: Miscible with Water
Typical Working
Concentration: 1.0 mL/L of Medium
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution: N/A
Other Notes: Contains the vitamins as described by Gamborg (1968).
Myo-Inositol may precipitate out of solution when cold; warming with
occasional agitation will redissolved the precipitate.
pH = 3.75 – 4.75

Application Notes
Plant Tissue Culture Tested
References
Gamborg, OL, RA Miller, K Ojima. 1968. Nutrient requirements of suspension cultures of
soybean root cells. Exp. Cell Research 50: 151-158.

HELLER BASAL SALT MIXTURE

HELLER BASAL SALT MIXTURE
Product ID: H393

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY HELLER (1953).

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

H393
Heller Basal Salt Mixture

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 1.64 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Heller (1953).
Application Notes
Plant Tissue Culture
References
Heller, R. 1953. Ann. Sci. Nat. Bot. Biol. Beg. 11th Ser. 14:1-223.

HELLER/WHITE MODIFIED BASAL SALT MIXTURE

HELLER/WHITE MODIFIED BASAL SALT MIXTURE
Product ID: H396

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY HELLER (1953) AND WHITE (1963). WITHOUT MOLYDENUM TRIOXIDE.
PLANT TISSUE CULTURE TESTED

H396
Heller/White Modified
Basal Salt Mixture

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 1.04 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Heller (1953) and White (1963).

Application Notes
Plant Tissue Culture
References
Heller, R. 1953. Ann. Sci. Nat. Bot. Biol. Beg. 11th Ser. 14:1-223.
White, PR. 1963. The Cultivation of Animal and Plant Cells, 2nd Edition, Ronald Press, NY, NY.

HOAGLAND MODIFIED BASAL SALT MIXTURE

HOAGLAND MODIFIED BASAL SALT MIXTURE
Product ID: H353

Storage Temperature: 2 to 6 C

Description:
CONTAINS FERROUS SULFATE AND THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY HOAGLAND AND ARNON (1950).
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

HOSTA INITIATION/MULTIPLICATION MEDIUM STAGE I/II MEDIUM

HOSTA INITIATION/MULTIPLICATION MEDIUM STAGE I/II MEDIUM
Product ID: H435

Storage Temperature: 2 to 6 C

Description: MODIFIED MURASHIGE & SKOOG W/(mg/L): 2.0 BA, 160 ADENINE HEMISULFATE, 500 CASEIN HYDROLYSATE, & .5 NAA
PLANT TISSUE CULTURE TESTED


H435
Hosta Initiation/ Multiplication Medium
Stage I/II Medium

Properties
Form: Fine to Fluffy Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 43.39 g/L
Storage Temp: 2-6°
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Murashige and
Skoog (1962) and the vitamins described by Linsmaier and Skoog (1965).
Also contains the supplements cited below.

Application Notes
Plant Tissue Culture Tested
Plant species: Hosta
Excellent stage I and II medium for Hosta cultures.
References
Murashige, T and F Skoog. 1962. A revised medium for rapid growth and bio-assays with tobacco tissue cultures. Physiologia Plantarum. 15: 473-497.
Linsmaier, EM and F Skoog. 1965. Organic growth factor requirements of tobacco tissue cultures. Physiol. Plant. 18: 100-127.

HOSTA MULTIPLICATION MEDIUM STAGE II MEDIUM

HOSTA MULTIPLICATION MEDIUM STAGE II MEDIUM
Product ID: H436

Storage Temperature: 2 to 6 C

Description: MODIFIED M & S W/(mg/L): 0.1 6- BENZYLAMINOPURINE, 160 ADENINE HEMISULFATE, 500 CASEIN HYDROLYSATE, & .5 NAA
PLANT TISSUE CULTURE TESTED

H436
Hosta Multiplication Medium
Stage II Medium

Properties
Form: Fine to Fluffy Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 43.39 g/L
Storage Temp: 2-6°
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Murashige and
Skoog (1962) and the vitamins described by Linsmaier and Skoog (1965).
Also contains the supplements cited below.

Application Notes
Plant Tissue Culture Tested
Plant species: Hosta
References
Murashige, T and F Skoog. 1962. A revised medium for rapid growth and bio-assays with tobacco tissue cultures. Physiologia Plantarum. 15: 473-497.
Linsmaier, EM and F Skoog. 1965. Organic growth factor requirements of tobacco tissue cultures. Physiol. Plant. 18: 100-127.

HOSTA ROOTING MEDIUM STAGE III MEDIUM

HOSTA ROOTING MEDIUM STAGE III MEDIUM
Product ID: H437

Storage Temperature: 2 to 6 C

Description: MODIFIED MURASHIGE & SKOOG (1962) WITH (MG/L): 0.1 BA, 500.0 CASEIN HYDROLYSATE, AND 0.5 NAA


H437
Hosta Rooting Medium
Stage III Medium
Properties
Form: Fine to Fluffy Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 43.23 g/L
Storage Temp: 2-6°
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Murashige and
Skoog (1962) and the vitamins described by Linsmaier and Skoog (1965).
Also contains the supplements cited below.

Application Notes
Plant Tissue Culture Tested
Plant species: Hosta
References
Murashige, T and F Skoog. 1962. A revised medium for rapid growth and bio-assays with tobacco tissue cultures. Physiologia Plantarum. 15: 473-497.
Linsmaier, EM and F Skoog. 1965. Organic growth factor requirements of tobacco tissue cultures. Physiol. Plant. 18: 100-127.

KAO & MICHAYLUK BASAL SALT MIXTURE

KAO & MICHAYLUK BASAL SALT MIXTURE
Product ID: K413

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS AS DESCRIBED BY KAO & MICHAYLUK (1975).
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

K413
Kao & Michayluk
Basal Salt Mixture
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.65 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients as described by Kao & Michayluk
(1975).

Application Notes
Plant Tissue Culture
Plant species: Vicia hajastana
This medium was originally developed for the culture of Vicia hajastana protoplasts. The culture of low cell densities (1-2 cells/ml) is enhanced when the medium is supplemented with organic acids, sugar alcohols, sugars, plant growth regulators and amino acids. (See K427) Cell growth and division could also be enhanced by raising the concentrations of calcium chloride from 1 to 5 mM.
References
Kao, KN and MR Michayluk. 1975. Nutritional requirements for growth of Vicia hajastana cells and protoplasts at a very low population density in liquid media. Planta 126:105-110.

KAO & MICHAYLUK MODIFIED BASAL MEDIUM

KAO & MICHAYLUK MODIFIED BASAL MEDIUM
Product ID: K427

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- & MICRONUTRIENTS, VITAMINS, & ORGANIC ACIDS AS DESCRIBED BY KAO & MICHAYLUK.
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

K427
KAO & MICHAYLUK
MODIFIED BASAL MEDIUM
Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 3.9 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble precipitates may form.
Other Notes: Contains the macro- and micronutrients, vitamins, and organic supplements as described by Kao and Michayluk (1975).

Application Notes
Plant Tissue Culture Tested
Plant species: Vicia hajastana
This medium was originally developed for the culture of Vicia hajastana protoplasts. The culture of low cell densities (1-2 cells/ml) is enhanced when the medium is supplemented with organic acids, sugar alcohols, sugars, plant growth regulators and amino acids. Cell growth and division could also be enhanced by raising the concentrations of calcium chloride from 1 to 5 mM.
References
Kao, KN and MR Michayluk. 1975. Nutritional requirements for growth of Vicia hajastana cells and protoplasts at a very low population density in liquid media. Planta 126:105-110.

KAO & MICHAYLUK VITAMIN SOLUTION (100x)

KAO & MICHAYLUK VITAMIN SOLUTION (100x)
Product ID: K421

Storage Temperature: 2 to 6 C

Description: USE AT A CONCENTRATION OF 10 mL/L OF MEDIUM TO ACHIEVE THE PROPER FINAL CONCENTRATION.

STERILE: PASSES USP STERILITY TESTING

PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 36/37/38 S: 26-36

K421
Kao & Michayluk Vitamin Solution (100x)

Properties
Form: Liquid
Appearance: Clear, Colorless to Slight Yellow Tint Solution
Application: Plant Tissue Culture
Solubility: Miscible with Water
Typical Working
Concentration: 10.0 mL/L of Medium
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution: N/A
Other Notes: Contains the vitamins as described by Kao and Michayluk (1975).

Application Notes
Plant Tissue Culture Tested
References
Kao, KN and MR Michayluk. 1975. Nutritional requirements for growth of Vicia hajastana cells and protoplasts at a very low population density in liquid media. Planta 126:105-110.

LINSMAIER & SKOOG BASAL MEDIUM

LINSMAIER & SKOOG BASAL MEDIUM
Product ID: L689

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- & MICRONUTRIENTS, & VITAMINS DESCRIBED BY LINSMAIER & SKOOG (1964).
This medium may be sold as Murashige & Skoog (MS) Medium with Minimal Organics (MSMO) by some media suppliers.
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 8-36/37/38 S: 17-26-36

L689
Linsmaier & Skoog
Basal Medium
Synonym: Murashige & Skoog (MS) Medium with Minimal Organics (MSMO)

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 4.43 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients and vitamins as described by
Linsmaier and Skoog (1965).
pH = 3.5 – 4.5

Application Notes
Plant Tissue Culture Tested
Plant species: Originally tobacco; since then many other species
This medium is the standard Murashige & Skoog (MS) basal salts supplemented with Linsmaier and Skoog vitamins. This medium is a subsequent optimization of the medium developed by Murashige and Skoog. Linsmaier’s research on the optimization of vitamins first described by Murashige as essential. Linsmaier found that certain vitamins were not essential when Thiamine•HCI was optimized from 0.1 to 0.4 mg/L. Linsmaier also noted that Folic acid, p-Aminobenzoic Acid, L-Glutamine, and Ascorbic Acid all had a positive influence on the growth of Nicotiana callus but was not as essential as Thiamine•HCI and myo-Inositol.
References
Linsmaier, EM and F Skoog. 1965. Organic growth factor requirements of tobacco tissue culture. Physiol. Plant. 18:100-127.

LINSMAIER & SKOOG BASAL MEDIUM W/ 30g/L SUCROSE & 7 g/L AGAR

LINSMAIER & SKOOG BASAL MEDIUM W/ 30g/L SUCROSE & 7 g/L AGAR
Product ID: L467

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO- AND MICRONUTRIENTS, AND VITAMINS AS DESCRIBED BY LINSMAIER & SKOOG (1965).
This medium may be sold as Murashige & Skoog (MS) Medium with Minimal Organics (MSMO) by some media suppliers.
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 36/37/38 S: 26-36

L467
Linsmaier & Skoog Basal Medium
w/ 30 g/L Sucrose and 7 g/L Agar
Synonym: Murashige & Skoog (MS) Medium with Minimal Organics (MSMO)

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 41.43 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients and vitamins as described by
Linsmaier and Skoog (1965).
pH = 4.25 – 5.25

Application Notes
Plant Tissue Culture Tested
Plant species: Originally tobacco; since then many other species
This medium is the standard Murashige & Skoog (MS) basal salts supplemented with Linsmaier and Skoog vitamins. This medium is a subsequent optimization of the medium developed by Murashige and Skoog. Linsmaier’s research on the optimization of vitamins first described by Murashige as essential. Linsmaier found that certain vitamins were not essential when Thiamine•HCI was optimized from 0.1 to 0.4 mg/L. Linsmaier also noted that Folic acid, p-Aminobenzoic Acid, L-Glutamine, and Ascorbic Acid all had a positive influence on the growth of Nicotiana callus but was not as essential as Thiamine•HCI and myo-Inositol.
References
Linsmaier, EM and F Skoog. 1965. Organic growth factor requirements of tobacco tissue culture. Physiol. Plant. 18:100-127.

LINSMAIER & SKOOG BASAL MEDIUM W/ 30g/L SUCROSE & 7g/L AGAR, pH ADJUSTED & BUFFERED

LINSMAIER & SKOOG BASAL MEDIUM W/ 30g/L SUCROSE & 7g/L AGAR, pH ADJUSTED & BUFFERED
Product ID: L452

Storage Temperature: 2 to 6 C

Description: CONTAINS THE MACRO-& MICRONUTRIENTS, & VITAMINS AS DESCRIBED BY LINSMAIER & SKOOG (1965)
PLANT TISSUE CULTURE TESTED

RISK & SAFETY: R: 36/37/38 S: 26-36

L452
Linsmaier & Skoog Modified Basal Medium
w/ 30 g/L Sucrose & 7 g/L Agar
pH Adjusted and Buffered
Synonym: Murashige & Skoog (MS) Medium with Minimal Organics (MSMO)

Properties
Form: Powder
Appearance: White to Yellow Powder
Application: Plant Tissue Culture
Solubility: Water
Typical Working
Concentration: 42.53 g/L
Storage Temp: 2 – 6° C
Storage Temp of
Stock Solution:
Preparation of concentrated solutions is not recommended as insoluble
precipitates may form.
Other Notes: Contains the macro- and micronutrients and vitamins as described by
Linsmaier and Skoog (1965).

Application Notes
Plant Tissue Culture Tested
This medium is the standard Murashige & Skoog (MS) basal salts supplemented with Linsmaier and Skoog vitamins. The medium is pH adjusted and buffered with MES. Under most circumstances, adjusting the pH is not necessary; simply add water and any desired PGR’s, gelling agent, or other supplements. The addition of MES will help to stabilize pH fluctuations during media preparation and culture.
References
Linsmaier, EM and F Skoog. 1965. Organic growth factor requirements of tobacco tissue culture. Physiol. Plant. 18:100-127.

Jumat, 09 Juli 2010

MEDIA KULTUR JARINGAN TUMBUHAN SIAP PAKAI YANG ADA DI PERDAGANGAN

Penulis : Agung Surono, S.Si

Pada mulanya media kultur jaringan harus dibuat dengan cara meracik sendiri dan kita kalau mau membuat media kultur jaringan harus mengumpulkan terlebih dahulu zat-zat kimia yang diperlukan untuk pembuatan media kultur jaringan. Dalam mengumpulkan zat-zat kimia yang diperlukan untuk pembuatan suatu media kultur jaringan ini tentunya dibutuhkan biaya yang besar. Kenapa diperlukan biaya yang besar untuk mengumpulkan zat-zat kimia yang diperlukan untuk pembuatan media kultur jaringan, hal ini dikarenakan untuk membeli zat-zat kimia tersebut tidak bisa dilakukan dengan cara mengecer, pembeliannya biasanya harus dalam ukuran kemasan tertentu. Dan zat-zat kimia tersebut belum tentu dalam kondisi ready stock dan kadang harus indent sampai beberapa bulan.

 


Sebagian kecil zat-zat kimia yang diperlukan untuk membuat media kultur jaringan

Belum lagi saat ini ada kendala lagi yaitu beberapa bahan kimia penyusun media kultur jaringan sangat sulit didapat karena zat tersebut bisa digunakan sebagai bahan peledak, bahan yang tersebut adalah ammonium nitrat. Pada saat ini tidak semua produsen zat kimia menjual bahan ammonium nitrat untuk umum dan untuk mendapatkannya harus dengan menggunakan surat end user asli dimana dalam surat end user tersebut pembeli harus membuat pernyataan bahwa ammonium nitrat tersebut hanya digunakan untuk keperluan laboratorium dan tidak akan menjual ammonium nitrat tersebut ke orang lain. Belum lagi saat ini HCl juga susah untuk mendapatkannya karena HCl termasuk bahan prekursur dan untuk mendapatkannya selain harus memakai surat end user juga harus membelinya langsung di PPI Jakarta sedangkan pedagang zat-zat kimia biasa saat ini tidak bisa lagi menjualnya karena adanya Undang-undang yang melarang dengan sanksi hukuman yang berat.
Selain diperlukan biaya yang mahal untuk meracik sendiri medium kultur jaringan juga untuk kegiatan menimbang lalu membuat larutan stok dan mencampur bahan-bahan tersebut menjadi media kultur ternyata cukup menyita waktu serta belum lagi adanya kemungkinan terjadinya kesalahan dalam mempersiapkan media kultur tersebut.
Dengan adanya beberapa hal yang menyulitkan tersebut di atas maka pada saat ini banyak laboratorium yang menggunakan media kultur siap pakai yang pada saat ini banyak terdapat dalam dunia perdagangan. Ada beberapa pabrik bahan kimia yang saat ini menjual campuran dari bahan kimia penyusun media tersebut dalam bentuk serbuk kering. Sebagai hasil dari dari pengalaman dalam menanam materi tanaman yang cukup banyak macamnya, doktor T. Murashige telah membuat sejumlah formulasi dari media kultur untuk propagasi secara in vitro yang memenuhi kebutuhan di masa sekarang ini.

 

Media Murashige & Skoog termasuk vitamin siap pakai produk Duchefa dalam kemasan 50 liter, 10 liter dan 1 liter


Media Murashige & Skoog dengan vitamin Gamborg B5 siap pakai produk Duchefa dalam kemasan 1 liter

Medium kultur Orchimax siap pakai produk dari Duchefa kemasan 1 liter

Media kultur MS siap pakai produk Phytotech

Media kultur MS siap pakai produk kemasan 1 liter produk Phytotech

Medium Linsmaier & Skoog siap pakai produk Phytotech

Medium kultur Ichihasi New Pahalaenopsis (NP) medium siap pakai produk dari Phytotech kemasan 10 liter

Pada saat ini ada beberapa industri bahan kimia seperti Duchefa, Phytotech, Caisson, MP Bio, Sigma yang telah menjual campuran mineral dan zat organik dari Murashige dan media organik dengan atau tanpa agar. Ada juga berbagai formulasi Murashige yang khusus dibuat untuk spesies-spesies yang biasa dipropagasikan telah ada dalam perdagangan. Beberapa jenis media kultur jaringan yang lain seperti Anderson's rhododendron medium, Chee and Pool Vitis medium, Chu (N6) medium, Ipomoea basal medium, De Greef and Jacobs medium, Juglans medium, Eriksson medium, Gamborg B5 medium, Gresshoff & Doy medium, Heller medium, Kao & michayluk medium, Knudson C Orchid medium, Lindemann Orchid medium
, Linsmaier & Skoog medium, Litvay medium, McCown Woody Plant medium, Murashige & Miller medium, Nitsch medium, NLN medium, Orchimax medium, Quoirin & Lepoivre medium, Rugini Olive medium, Shenk & Hildebrandt medium, S-medium Milieu S Milieu de Bouturage, Westvaco WV5 medium, Vacin & Went medium, White medium dan lain-lain juga sudah bisa didapatkan di pasaran perdagangan.
Dalam membuat media kultur jaringan dari campuran serbuk yang siap pakai ini dilakukan hanya dengan melarutkan dalam jumlah tertentu air yang kualitasnya memenuhi persyaratan, lalu menyesuaikan pHnya lalu memasukkan ke dalam wadah-wadah dan selanjutnya mensterilkannya. Untuk melarutkan campuran media kultur yang mengandung agar diperlukan pemanasan yang secukupnya. Dan untuk mendapatkan media-media yang sesuai, dapat dilakukan dengan membeli campuran dari formulasi dasar, lalu kemudian ditambahkan hormon atau zat pengatur tumbuh serta bahan-bahan lain yang sesuai dengan yang dibutuhkan.
GIBCO Laboratories pada saat ini telah menginformasikan bahwa mereka telah memasarkan jenis formulasi baru, terdiri campuran serbuk media kultur yang telah di buffer pada pH 5,7. Dan pada akhit-akhir ini GIBCO Laboratories juga telah memasarkan media kultur dengan nama "Nutri-Tubed" yang betul-betul siap pakai dan telah diosterilkan dalam wadah kultur.
Pada saat ini pembuatan media dengan cara menimbang dan mencampur bahan-bahan dasar, dilakukan kalau dirasa perlu untuk coba-coba atau bila komposisi dari suatu formulasi yang dibutuhkan tidak tersedia di dunia perdagangan.
Bagi yang membutuhkan media siap pakai yang seperti tersebut di atas bisa mengontak penulis : 


Agung Surono, S.Si 
dengan no.telp 08562927655 
atau bisa juga menghubungi via email di agungsurono@yahoo.com 

dan untuk pembelian paket kemasan 1 liter media MS didalamnya terdapat medium dasar MS termasuk vitamin, 30 gr gula, 8 gram agar serta anti kontaminasi jamur dan bakteri berupa PPM 1 ml.

Referensi :
Wetherel, D. F. 1982. Pengantar Propagasi Tanaman Secara In Vitro.. Avery Publishing Group Inc. New Jersey. pp. 51.

MACAM-MACAM PENUTUP BOTOL KULTUR

Penulis : Agung Surono, S.Si

Penutup botol kultur jaringan yang sering digunakan di antarnya adalah gumpalan kapas, aluminium foil dan tutup dari logam atau polipropilen.
Untuk penggunaan gumpalan kapas yang dibuat dengan baik untuk penutup botol kultur jaringan merupakan pelindung terhadap kontaminasi mikrobia udara yang paling baik akan tetapi kelemahannya dibutuhkan waktu yang lama untuk membuatnya, selain itu menyebabkan terjadinya penguapan uap air uyang cepat dan apabila dipakai berulang kali akan cepat rusak. Dan pada saat ini sudah jarang yang menggunakan gumpalan kapas ini sebagai penutup botol kultur jaringan.

Petupup botol kultur dari plastik yang dibagian tengahnya gumpalan kapas

Pada botol kultur bisa juga mengunaan penutup dari plastik yang ditengahnya berlubang dan bagian yang berlubang ini dipasangi gumpalan kapas. Tutup botol kultur model ini banyak dipakai untuk botol kultur yang berisi media yang digunakan untuk budidaya perkecambahan biji anggrek. Tutup botol ini bisa dipakai berulang kali dengan penggantian gumpalan kapas. Dn untuk lebih merapatkan penutupan di bagian luarnya diberi plastik.

Aluminium foil sebagai penutup botol kultur jaringan

Pada umumnya dalam budidaya jaringan yang biasa digunakan sebagai penutup botol kultur adalah aluminium foil. Aluminium foil dipotong persegi dan ukuran potongan aluminium foil dibuat sedemikian rupa sehingga aluminium foil tersebut menutupi bagian terbuka dari botol kultur sampai 2 inchi ke bawah pada tepi botol kultur atau wadah lainnya. Karena aluminium foil ini dapat menutup dengan rapat maka penguapan dapat sangat berkurang. Dan untuk lebih merapatkan penutupan dapat dipakai karet gelang. Aluminium foil tahan panas sehingga pada saat pembuatan media setelah media dimasukkan ke dalam botol dan kemudian disterilkan dengan menggunakan autoclaf maka dengan aluminium foil ini tidak masalah karena aluminium foil sifatnya tahan panas. Akan tetapi pasa saat penanaman eksplan kadang saat membuka penutup botol yang berupa aluminium foil ini kalau tidak hati-hati kadang aluminium foil yang kualitasnya jelek karena tipis akan mudah sekali robek akibatnya harus mengganti dengan potongan aluminium foil yang baru. Untuk itu pada umumnya pada saat penanaman eksplan atau pada saat subkultur perlu disediakan potongan aluminium foil yang juga sudah disterilkan.Dan pada saat menutup botol kultur dengan menggunakan aluminium foil kalau tidak hati-hati aluminium foil ini bisa melaukai tangan. Dan selain itu aluminium foil ini harganya lumayan mahal dan umumnya hanya bisa digunakan untuk sekali pakai.

Botol kultur dari bekas botol obat dengan tutup botol asli dari logam

Selain itu ada pula yang menggunakan botol bekas obat untuk botol kultur sehingga untuk tutupnya digunakan tutup botolnya yang terbuat dari logam dan untuk menambah kerapatan penutupan botol kulturnya ditambah lagi lembaran plastik atau plastik wrap untuk menutupi lagi bagian luarnya. Tutup dari logam ini bisa dipakai berulang kali.

Penggunaan tutup plstik pada botol kultur dari bekas jam

Kemudian untuk botol kultur jaringan yang menggunakan botol bekas jam bisa kita gunakan penutup dari cetakan plastik, penutup ini tahan panas, bisa digunakan berulang kali hanya lama kelamaan penutup ini bisa juga menjadi rusak. Dan kelemahan penutup botol ini harga persatuannya lebih mahal daripada harga sepotong aluminium foil dan untuk mendapatkannya harus membeli dalam jumlah banyak.

Penutup botol kultur dari lembaran plastik dan dibantu dengan karet gelang untuk membantu merapatkan penutupan

Kemudian untuk lebih menghemat ada yang memakai lembaran plastik tahan panas untuk penutup botol kultur. Untuk penggunaan lembaran plastik ini kelemahannya harus menggunakan karet gelang untuk membantu merapatkan penutupannya. Dan saat ini banyak pengkultur yang menggunakan lembaran plastik dan karet gelang ini karena terbilang murah. Pada pemakaian lembaran plastik sebagai penutup botol kultur ini bisa digunakan mulai dari pembuatan media sampai penanaman eksplan.

Plastik wrap yang digunakan untuk menutup botol kultur

Dan yang sedang kami lakukan uji coba saat ini adalah menggunalan plastik wrap untuk menutup botol kultur jaringan. Pada mulanya penulis ragu untuk menggunakan lastik wrap untuk penutup botol kultur yang telah diisi eksplan atau bahan kultur lainnya. Penulis ragu menggunakan plastik wrap ini karena memikirkan bagaimana cara untuk mensterilkan sebelum digunakan untuk menutup botol kultur. Akan tetapi melihat keberhasilan teman kami dalam menggunakan plastik wrap ini di Laboratorium kultur jaringan tumbuhan di Fakultas Farmasi Universitas Sanata Dharma Yogyakarta, maka penulis melihat dan langsung praktek cara menutup botol kultur dengan plastik wrap. Dan setelah itu mencobanya di laboratorium yang ada di kantor. Setelah kita coba dan hasilnya sampai satu bulan ini baik media maupun eksplan tidak mengalami kontaminasi maka penulis yakin plastik wrap bisa digunakan sebagai alternatif untuk penutup botol kultur jaringan. Hanya saja pada saat membuat media kita masih menggunakan aluminium foil untuk menutup botol kultur dan plastik wrap hanya digunakan setelah botol kultur yang berisi media ditanami eksplan. Akan tetapi paling tidak plastik wrap bisa sebagai alternatif untuk penutup botol kultur jaringan. Dan mungkin saat ini yang menggunakan baru penulis dan Laboratorium kultur jaringan tumbuhan di Fakultas Farmasi Universitas Sanata Dharma Yogyakarta.

Referensi :

Wetherel, D. F. 1982. Pengantar Propagasi Tanaman Secara In Vitro.. Avery Publishing Group Inc. New Jersey. pp. 64-65.