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Merck
CN
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主要文件

安全信息

05-554

Sigma-Aldrich

抗KDR / Flk-1 / VEGFR2抗体,克隆CH-11

clone CH-11, Upstate®, from mouse

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About This Item

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物来源

mouse

质量水平

抗体形式

purified antibody

抗体产品类型

primary antibodies

克隆

CH-11, monoclonal

种属反应性

human, mouse

包装

antibody small pack of 25 μg

制造商/商品名称

Upstate®

技术

ELISA: suitable
immunocytochemistry: suitable
western blot: suitable

同位素/亚型

IgG1

NCBI登记号

UniProt登记号

运输

ambient

靶向翻译后修饰

unmodified

基因信息

human ... KDR(3791)

特异性

KDR/Flk-1

免疫原

对应于鼠 KDR/Flk-1 残基 1158-1345 的重组蛋白

应用

抗 KDR/Flk-1/VEGFR2 抗体,克隆 CH-11 检测 KDR/Flk-1/VEGFR2 水平&,经发表 & 验证可用于 ELISA,IC & WB。

质量

通过免疫印迹对 HUVEC 细胞的 RIPA 裂解液进行了常规评估

目标描述

230kDa

外形

20mM 磷酸钠,pH 7.6、250mM NaCl 和 0.1% 叠氮化钠
形式:纯化的

其他说明

请参考特定批次的数据表。

法律信息

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

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Ashok Aspatwar et al.
Journal of enzyme inhibition and medicinal chemistry, 35(1), 109-117 (2019-11-07)
With the aim to obtain novel compounds possessing both strong affinity against human carbonic anhydrases and low toxicity, we synthesised novel thiourea and sulphonamide derivatives 3, 4 and 10, and studied their in vitro inhibitory properties against human CA I, CA
Eva Torres et al.
Antiviral research, 99(3), 281-291 (2013-06-27)
We here report on the synthesis of new series of polycyclic amines initially designed as ring-rearranged analogs of amantadine and featuring pentacyclo, hexacyclo, and octacyclo rings. A secondary amine, 3-azahexacyclo[7.6.0.0¹,⁵.0⁵,¹².0⁶,¹⁰.0¹¹,¹⁵]pentadeca-7,13-diene, 3, effectively inhibited A/M2 proton channel function, and, moreover, possessed
Rosana Leiva et al.
European journal of medicinal chemistry, 139, 412-428 (2017-08-19)
Recent findings suggest that treatment with 11β-HSD1 inhibitors provides a novel approach to deal with age-related cognitive dysfunctions, including Alzheimer's disease. In this work we report potent 11β-HSD1 inhibitors featuring unexplored pyrrolidine-based polycyclic substituents. A selected candidate administered to 12-month-old
Ornella Di Pietro et al.
European journal of medicinal chemistry, 84, 107-117 (2014-07-13)
Optimization of an essentially inactive 3,4-dihydro-2H-pyrano[3,2-c]quinoline carboxylic ester derivative as acetylcholinesterase (AChE) peripheral anionic site (PAS)-binding motif by double O → NH bioisosteric replacement, combined with molecular hybridization with the AChE catalytic anionic site (CAS) inhibitor 6-chlorotacrine and molecular dynamics-driven
J F Höfling et al.
Brazilian journal of biology = Revista brasleira de biologia, 70(4), 1065-1068 (2010-12-25)
The increase in the resistance to antimicrobial drugs in use has attracted the attention of the scientific community, and medicinal plants have been extensively studied as alternative agents for the prevention of infections. The Candida genus yeast can become an

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