A4800
琼脂
Type M, suitable for plant cell culture
别名:
琼脂-琼脂, 胶琼脂
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线性分子式:
(C12H18O9)n
化学文摘社编号:
UNSPSC Code:
50405901
eCl@ss:
42040102
EC Number:
232-658-1
NACRES:
NA.21
MDL number:
产品名称
琼脂, Type M, suitable for plant cell culture
SMILES string
O1[C@@H]([C@@H]([C@@H]([C@H](C1OC2[C@H]3OCC2OC([C@H]3O)C)O)OC)O)CO
InChI
1S/C14H24O9/c1-5-8(16)13-11(7(21-5)4-20-13)23-14-10(18)12(19-2)9(17)6(3-15)22-14/h5-18H,3-4H2,1-2H3/t5?,6-,7?,8-,9+,10-,11?,12+,13+,14?/m1/s1
InChI key
GYYDPBCUIJTIBM-DYOGSRDZSA-N
biological source
algae (Rhodophyceae)
type
Type M
form
powder
technique(s)
cell culture | plant: suitable
transition temp
transition temp 34-36 °C
application(s)
agriculture
storage temp.
room temp
Quality Level
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Application
Type M agar has been used as a component of Murashige and Skoog (MS) medium for culturing Arabidopsis thalania seeds. It has also been used in rooting media for tomato (Solanum lycopersicum) seeds.
General description
Type M agar is predominantly used in plant tissue culture. It is similar to agar, a polysaccharide complex with a backbone of alternating agarose and agaropectin molecules and extracted from red algae.
存储类别
11 - Combustible Solids
wgk
WGK 1
ppe
Eyeshields, Gloves, type N95 (US)
Sangeeta Negi et al.
The Plant journal : for cell and molecular biology, 61(1), 3-15 (2009-10-02)
In this study we investigated the role of ethylene in the formation of lateral and adventitious roots in tomato (Solanum lycopersicum) using mutants isolated for altered ethylene signaling and fruit ripening. Mutations that block ethylene responses and delay ripening -Nr
Sanjaya B Ekanayake et al.
Methods in molecular biology (Clifton, N.J.), 1305, 223-240 (2015-04-26)
One of the most striking features of plant mitochondria when visualized in living tissue is their dynamism. The beauty of cytoplasmic streaming, driving, and being driven by the motility of mitochondria and other small organelles belies the complexity of the
Xiaohua Wang et al.
Nature protocols, 10(12), 2054-2063 (2015-11-20)
Measuring the mobility and interactions of proteins is key to understanding cellular signaling mechanisms; however, quantitative analysis of protein dynamics in living plant cells remains a major challenge. Here we describe an automated, single-molecule protocol based on total internal reflection
Extraction and characterization of agar from Australian Pterocladia lucida
Chiovitti A, et al.,
Journal of Applied Phycology, 16(1), 41-48 (2004)
Arnaud Dechesne et al.
Applied and environmental microbiology, 74(16), 5195-5200 (2008-07-01)
Water is arguably the most important constituent of microbial microhabitats due to its control of physical and physiological processes critical to microbial activity. In natural environments, bacteria often live on unsaturated surfaces, in thin (micrometric) liquid films. Nevertheless, no experimental
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