05-710
抗-NG2抗体，克隆132.38
clone 132.38, Upstate®, from mouse
别名:
Anti-CSPG4A, Anti-HMW-MAA, Anti-MCSP, Anti-MCSPG, Anti-MEL-CSPG, Anti-MSK16, Anti-NG2
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关于此项目
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
132.38, monoclonal
Species reactivity:
rat, mouse
Application:
IHC, WB
Citations:
29
biological source
mouse
Quality Level
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
132.38, monoclonal
species reactivity
rat, mouse
manufacturer/tradename
Upstate®
technique(s)
immunohistochemistry: suitable, western blot: suitable
isotype
IgG1
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
mouse ... Cspg4(121021)
rat ... Cspg4(81651)
General description
~270-300 kDa
Immunogen
HEK293细胞表达由氨基酸1592-2222组成的截短完整膜形式的NG2
Application
抗NG2抗体，克隆132.38，可检测NG2的水平 & 已出版&并经过验证可用于IH & WB。
研究子类别
神经 & 胶质标记
神经 & 胶质标记
研究类别
神经科学
神经科学
预期与小鼠发生交叉反应。
Biochem/physiol Actions
识别NG2。
Physical form
形式：纯化
蛋白A纯化的免疫球蛋白，溶于0.1M Tris-甘氨酸（pH 7.4）、0.15M NaCl和0.05％叠氮化钠作为防腐剂的缓冲液中。
蛋白G纯化
Preparation Note
自运送之日起在-20°C可稳定保存2年。避免反复冻融。为了最大程度地回收产品，在融化后和取下盖子之前，将原始样品瓶进行离心。
Analysis Note
对照
脑组织
脑组织
通过免疫印迹对整个鼠脑制剂进行了常规评估
Other Notes
浓度：请参考批次特异性浓缩物的分析证书。
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
除非我们的产品目录或产品附带的其他公司文档另有说明，否则我们的产品仅供研究使用，不得用于任何其他目的，包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
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存储类别
10 - Combustible liquids
wgk
WGK 1
Dongying Chen et al.
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Fibronectin (Fn1) is an evolutionarily conserved extracellular matrix glycoprotein essential for embryonic development. Global deletion of Fn1 leads to mid-gestation lethality from cardiovascular defects. However, severe morphogenetic defects that occur early in embryogenesis in these embryos precluded assigning a direct
In vivo intracellular recording suggests that gray matter astrocytes in mature cerebral cortex and hippocampus are electrophysiologically homogeneous.
Mishima, T; Hirase, H
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Antiangiogenic drugs have been used as anticancer agents to target tumor endothelial cells or pericytes. Because of limited efficacy of the current monotherapies, there is a strong demand for the dual targeting of endothelial cells and pericytes. Here, we identify