G1019
Gamborg′s Vitamin Solution
1000 ×, liquid, suitable for plant cell culture
Synonym(s):
Gamborg Vitamin Solution, Vitamin Solution
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About This Item
UNSPSC Code:
10171502
NACRES:
NA.72
Recommended Products
sterility
sterile-filtered
Quality Level
form
liquid
concentration
1000 ×
technique(s)
cell culture | plant: suitable
color
colorless
pH
5.0-7.0
application(s)
agriculture
storage temp.
2-8°C
Application
Gamborg′ B-5 medium described by Gamborg, et al. may be purchased as a complete medium (G5893) or reconstituted from Vitamin 1000x (G1019) and Basal Salt Mixture (G5768) chemstocks. Use Gamborg′s B-5 (B5) medium for in vitro plant culture of cell lines and tissues such as of Taxus globosa, Splachnum ampullaceum Hedw, Linum album, Eucalyptus camaldulensis. Gamborg′s B-5 medium has been used for the culture of Annona squamosa callus.
Use at a concentration of one ml per liter of prepared medium to achieve the proper final concentration.
Components
Solution contains (mg/ml): 100.0 myo-inositol, 1.0 nicotinic acid, 1.0 pyridoxine hydrochloride, 10.0 thiamine hydrochloride.
Related product
Product No.
Description
Pricing
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Biotechnology letters, 30(9), 1671-1677 (2008-04-23)
Cell suspension cultures of Linum album were developed from internode portions of in vitro germinated plant in Gamborg's B5 medium supplemented with 0.4 mg naphthalene acetic acid/l. The highest biomass was 8.5 g/l with podophyllotoxin and 6-methoxypodophyllotoxin at 29 and
R Mallon et al.
Cryo letters, 31(1), 24-28 (2010-03-24)
The source of germplasm as well as the technique used for storage of mosses can enhance survival after cryopreservation. Samples of gametophores, protonemata and protonemal brood cells from in vitro cultures of Splachnum ampullaceum were cryopreserved following exposure to a
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Journal of Asian natural products research, 4(3), 171-174 (2002-07-18)
Callus cultures of Annona squamosa were induced using different explants including petals, seed contents (megagametophyte and embryo) and fruits (mesocarp). Growth of the calli induced from the explants was found to be influenced by the type, concentration and ratio of
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