产品货号:
Z24364
中文名称:
Prohibitin/PHB抗体
英文名称:
Anti-Prohibitin/PHB Antibody
产品规格:
50μl|100μl|150μl
发货周期:
1~3天
产品价格:
询价
抗体名称 | Anti-Prohibitin/PHB Antibody |
指标别名 | Cell and organelle markers;Mitochondria Marker;Mitochondrial Marker;Mitochondrion Marker;PHB;PHB1;prohibiti |
克隆性 | Polyclonal |
检验物种 | human,mouse,rat |
应用范围 | WB,IHC,ELISA |
基因名称 | PHB |
抗体来源 | Rabbit |
抗体类型 | IgG |
免疫原 | E.coli-derived human Prohibitin/PHB recombinant protein (Position:M1-I257). |
实际分子量 | 30KD |
成分 | 500μg/mL antibody with PBS,0.02% NaN3,1mg BSA and 50% glycerol. |
纯化方式 | Immunogen affinity purified. |
浓度 | 500μg/mL |
产品形态 | 溶液 |
保存条件 | 12 months from date of receipt,-20℃ as supplied.6 months 2 to 8℃ after reconstitution.Avoid repeated freezing and thawing. |
背景资料 | PHB(Prohibitin),also known as PHB1,is a protein that in humans is encoded by the PHB gene.White et al.(1991) mapped the PHB gene to chromosome 17 by analysis of human-mouse somatic cell hybrid cell lines using a genomic fragment of human prohibitin DNA isolated from a library using the rat prohibitin cDNA clone.By in situ hybridization,they localized the gene to 17q21.Sato et al.(1992) isolated the human homolog of the rat prohibitin gene and mapped it to 17q12-q21 by in situ hybridization.Proliferation of tumor cells depends on new blood vessel formation(angiogenesis) that accompanies malignant progression.Anticancer therapies using angiogenesis inhibitors or cytotoxic agents targeted to the vasculature of tumors have been evaluated in clinical trials.Although white fat is a nonmalignant tissue,it has the capability to quickly proliferate and expand.Furthermore,it is highly vascularized.Rupnick et al.(2002) showed that nonspecific angiogenesis inhibitors can prevent the development of obesity of mice. |
Uniprot ID | P35232 |
推荐配套试剂 | Biorab recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ZN1926) for Western blot. |
基因名全称 | prohibitin |
蛋白名全称 | Prohibitin |
推荐稀释比 | Western blot(WB) 1:500~2000 Immunohistochemistry in paraffin section IHC 1:50~400 ELISA 1:100~1000 (Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
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