所有图片(1)
About This Item
线性分子式:
[Co(NH3)6]Cl3
CAS号:
分子量:
267.48
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.52
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一般描述
六胺钴 (III) 被认为是完全溶剂化镁的类似物，能够激活一些需要镁的酶。在 DNA 缩合研究中是有用的。
应用
适用于
- DNA 缩合研究
- 诱导 DNA 从 B 型向 A 型或 Z 型转化
- 核酸晶体生长诱导
- 三级 tRNA 相互作用的稳定性
- 连接缓冲液的制备
警示用语：
Danger
危险分类
Aquatic Chronic 4 - Carc. 2 - Resp. Sens. 1 - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Filip Senigl et al.
Cell reports, 29(12), 3902-3915 (2019-12-19)
Somatic hypermutation (SHM) introduces point mutations into immunoglobulin (Ig) genes but also causes mutations in other parts of the genome. We have used lentiviral SHM reporter vectors to identify regions of the genome that are susceptible ("hot") and resistant ("cold")
J S Kieft et al.
Structure (London, England : 1993), 5(5), 713-721 (1997-05-15)
Solvated metal ions are critical for the proper folding and function of RNA. Despite the importance of these ions, the details of specific metal ion-RNA interactions are poorly understood. The crystal structure of a group I intron ribozyme domain characterized
T Allers et al.
Nucleic acids research, 28(2), e6-e6 (1999-12-22)
The Holliday junction is a central intermediate in genetic recombination. This four-stranded DNA structure is capable of spontaneous branch migration, and is lost during standard DNA extraction protocols. In order to isolate and characterize recombination intermediates that contain Holliday junctions
M C Whitby et al.
The Journal of biological chemistry, 273(31), 19729-19739 (1998-07-25)
The RecG protein of Escherichia coli is a junction-specific DNA helicase that drives branch migration of Holliday intermediates in genetic recombination and DNA repair. The reaction was investigated using synthetic X-junctions. RecG dissociates X-junctions to flayed duplex products, although DNA
K L Kindle
Proceedings of the National Academy of Sciences of the United States of America, 87(3), 1228-1232 (1990-02-01)
By using a method in which cell-wall-deficient Chlamydomonas reinhardtii cells were agitated in the presence of DNA, glass beads, and polyethylene glycol, nuclear transformation rates of approximately 10(3) transformants per micrograms of plasmid DNA were achieved. The nitrate reductase gene
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