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特異性
KDR/Flk-1
免疫原
对应于鼠 KDR/Flk-1 残基 1158-1345 的重组蛋白
應用
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。
品質
通过免疫印迹对 HUVEC 细胞的 RIPA 裂解液进行了常规评估
標靶描述
230kDa
外觀
20mM 磷酸钠，pH 7.6、250mM NaCl 和 0.1％ 叠氮化钠
形式：纯化的
其他說明
请参考特定批次的数据表。
法律資訊
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
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儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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
Aleksandar Pashev et al.
Beilstein journal of organic chemistry, 16, 1456-1464 (2020-07-11)
The Castagnoli-Cushman reaction of 3,4-dihydroisoquinolines with glutaric anhydride, its oxygen and sulfur analogues was investigated as a one-step approach to the benzo[a]quinolizidine system and its heterocyclic analogs. An extension towards the pyrrolo[2,1-a]isoquinoline system was achieved with the use of succinic
Nikola Burdzhiev et al.
Molecules (Basel, Switzerland), 25(17) (2020-08-23)
Tautomerization of 2-phenylimidazolecarbaldehydes has not been studied in detail so far, although this process is a well-known phenomenon for imidazole derivatives. That is why we focus our study on a series of 2-phenylimidazolecarbaldehydes and their parent alcohols that were synthesized
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
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
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