05-554
抗KDR / Flk-1 / VEGFR2抗体，克隆CH-11
clone CH-11, Upstate®, from mouse
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关于此项目
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
CH-11, monoclonal
Application:
ELISA
immunocytochemistry
western blot
immunocytochemistry
western blot
Species reactivity:
human, mouse
Citations:
59
Technique(s):
ELISA: suitable
immunocytochemistry: suitable
western blot: suitable
immunocytochemistry: suitable
western blot: suitable
Uniprot accession no.:
产品名称
抗KDR / Flk-1 / VEGFR2抗体，克隆CH-11, clone CH-11, Upstate®, from mouse
biological source
mouse
conjugate
unconjugated
antibody form
purified antibody
antibody product type
primary antibodies
clone
CH-11, monoclonal
species reactivity
human, mouse
packaging
antibody small pack of 25 μg
manufacturer/tradename
Upstate®
technique(s)
ELISA: suitable
immunocytochemistry: suitable
western blot: suitable
isotype
IgG1
NCBI accession no.
UniProt accession no.
shipped in
ambient
target post-translational modification
unmodified
Quality Level
Gene Information
human ... KDR(3791)
相关类别
Analysis Note
通过免疫印迹对 HUVEC 细胞的 RIPA 裂解液进行了常规评估
Application
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。
Biochem/physiol Actions
KDR/Flk-1
General description
230kDa
Immunogen
对应于鼠 KDR/Flk-1 残基 1158-1345 的重组蛋白
Other Notes
请参考特定批次的数据表。
Physical form
20mM 磷酸钠，pH 7.6、250mM NaCl 和 0.1％ 叠氮化钠
形式：纯化的
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
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存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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
Rebecca R Foster et al.
The American journal of pathology, 173(4), 938-948 (2008-09-06)
We have previously reported expression of vascular endothelial growth factor (VEGF)-A and -C in glomerular podocytes and actions of VEGF-A on glomerular endothelial cells (GEnC) that express VEGF receptor-2 (VEGFR-2). Here we define VEGFR-3 expression in GEnC and investigate the
Mária Báthori et al.
Journal of chromatographic science, 42(5), 275-279 (2004-06-11)
A suitable combination of preparative scale separation methods results in effective clean-up of the ecdysteroids of Silene italica ssp. nemoralis (Waldst. and Kit.) Nyman. The isolation of minor ecdysteroids from the partially purified extract is based on the use of
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
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