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Merck
CN

A2536

Sigma-Aldrich

L -2-氨基丁酸

BioReagent, suitable for cell culture

别名:

L-α-氨基丁酸

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About This Item

经验公式(希尔记法):
C4H9NO2
CAS号:
分子量:
103.12
Beilstein:
1720935
EC 号:
MDL编号:
UNSPSC代码:
12352205
PubChem化学物质编号:
NACRES:
NA.75

生物来源

Porcine kidney
microbial
plant

质量水平

产品线

BioReagent

形式

powder

技术

cell culture | mammalian: suitable

溶解性

water: 50 mg/mL, clear, colorless

运输

ambient

储存温度

room temp

SMILES字符串

CC[C@H](N)C(O)=O

InChI

1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1

InChI key

QWCKQJZIFLGMSD-VKHMYHEASA-N

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相关类别

一般描述

L-苏氨酸和 L-天冬氨酸经-转氨基反应合成 L-2-氨基丁酸。它是一种带有乙基侧链的 L-丙氨酸类似物。

生化/生理作用

L-α-氨基丁酸 (AABA) 是非天然氨基酸氨基丁酸的异构体,在 γ-谷氨酰循环中具有调节谷胱甘肽生物合成的活性。最近研究了 AABA 作为体外成熟培养液(NCSU 23 培养液)的补充,用于卵母细胞和胚胎的培养。本品已确认可用于细胞培养。在肽功能的研究中,AABA 也被用作丙氨酸的替代氨基酸。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

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, Faceshields, Gloves


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A one-pot system for production of L-2-aminobutyric acid from L-threonine by L-threonine deaminase and a NADH-regeneration system based on L-leucine dehydrogenase and formate dehydrogenase
Tao R, et al.
Biotechnology Letters, 36(4), 835-841 (2014)
l-2-Aminobutyric acid: two fully ordered polymorphs with Z?= 4
Gorbitz CH
Acta Crystallographica Section B, Structural Science, 66(2), 253-259 (2010)
Cornelia Reimmann et al.
Journal of bacteriology, 186(19), 6367-6373 (2004-09-18)
In Pseudomonas aeruginosa, the antibiotic dihydroaeruginoate (Dha) and the siderophore pyochelin are produced from salicylate and cysteine by a thiotemplate mechanism involving the peptide synthetases PchE and PchF. A thioesterase encoded by the pchC gene was found to be necessary
Izumi Kawabata et al.
Nature communications, 3, 722-722 (2012-03-08)
Synaptic remodelling coordinated with dendritic growth is essential for proper development of neural connections. After establishment of synaptic contacts, synaptic junctions are thought to become stationary and provide fixed anchoring points for further dendritic growth. However, the possibility of active
Danica P Galonić et al.
Nature chemical biology, 3(2), 113-116 (2007-01-16)
Enzymatic incorporation of a halogen atom is a common feature in the biosyntheses of more than 4,500 natural products. Halogenation of unactivated carbon centers in the biosyntheses of several compounds of nonribosomal peptide origin is carried out by a class

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