biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
HMab-1, monoclonal
form
buffered aqueous solution
mol wt
antigen ~43 kDa
species reactivity
human
concentration
~1.0 mg/mL
technique(s)
western blot: 4.0-8.0 μg/mL using extract of HEK-293T cells overexpressing IDH1R132H.
UniProt accession no.
application(s)
research pathology
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... IDH1(3417)
General description
鼠抗IDH1(R132H)单克隆抗体(小鼠IgG1同种型)源自杂交瘤HMab1。这一杂交瘤是用对应人IDH1突变R132H 的多肽对 BALB/c 小鼠进行免疫接种后,取脾细胞与小鼠骨髓瘤细胞融合产生。异柠檬酸脱氢酶(IDH)家族成员IDH1是人细胞质NADP特异性酶。其亚细胞定位显示在过氧化物酶体和细胞质中。
Immunogen
与人 IDH1 突变 R132H 相对应的的肽。
Application
抗-IDH1(R132H)抗体用于:
- 免疫印迹
- 免疫组化
- 蛋白印迹
- 细胞周期分析和凋亡测定
- 染色质免疫沉淀(ChIP)测定
- 体外 迁移实验
Biochem/physiol Actions
异柠檬酸脱氢酶1(IDH1)将 NADP 作为共底物,催化异柠檬酸氧化脱羧成 α α -KG。IDH1 突变为 Arg132(R132)特有,这一突变使其具有生成2-羟基戊二酸(2HG)(而不是 α-KG)的功能。此产品通过影响 DNA 和组蛋白甲基化,改变基因转录。存在几种 IDH1 突变,包括 R132H、R132C、R132S、R132G 和 R132L。每种突变都可能导致不同肿瘤类型,具有不同恶性进展。最常见的突变(>90%)是精氨酸变为组氨酸(R132H)。 因此,识别 IDH1R132H 突变的抗体可用于诊断携带突变的肿瘤(如神经胶质瘤)。
Physical form
0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。
Disclaimer
除非我们的产品目录或产品随附的其他公司文件中另有说明,否则我们的产品仅用于研究用途,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、体外或体内治疗用途或任何类型的人类或动物消费或应用。
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存储类别
10 - Combustible liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
低风险生物材料
常规特殊物品
此项目有
IDH1R132H decreases the proliferation of U87 glioma cells through upregulation of microRNA-128a
Nie Q M, et al.
Molecular Medicine Reports, 12(5), 6695-6701 (2015)
Peroxisomal localization and function of NADP+-specific isocitrate dehydrogenases in yeast
Lu Q and McAlister-H L.
Archives of Biochemistry and Biophysics, 493(2), 125-134 (2010)
Expression of Idh1R132H in the murine subventricular zone stem cell niche recapitulates features of early gliomagenesis
Bardella C, et al.
Cancer Cell, 30(4), 578-594 (2016)
Molecular mechanisms of isocitrate dehydrogenase 1 (IDH1) mutations identified in tumors: the role of size and hydrophobicity at residue 132 on catalytic efficiency
Matteo D A, et al.
The Journal of biological chemistry, 292(19), 7971-7983 (2017)
Shuchen Chen et al.
Cancer medicine, 11(22), 4122-4133 (2022-05-09)
Isocitrate dehydrogenase (IDH) is an appealing target for anticancer therapy, and IDH (IDH1/2) inhibitors have been approved for targeted therapy of acute myeloid leukemia (AML) and Cholangiocarcinoma. The therapeutic potential of IDH inhibitors for non-small-cell lung cancer (NSCLC) patients is
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