FITC标记的Rho GTP酶激活蛋白36抗体
产品名称: FITC标记的Rho GTP酶激活蛋白36抗体
英文名称: Anti-ARHGAP36/FITC
产品编号: HZ-18116R-FITC
产品价格: null
产品产地: 中国/上海
品牌商标: HZbscience
更新时间: 2023-08-17T10:24:20
使用范围: ICC=1:50-200 IF=1:50-200
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Rabbit Anti-ARHGAP36/FITC Conjugated antibody
FITC标记的Rho GTP酶激活蛋白36抗体
英文名称 | Anti-ARHGAP36/FITC |
中文名称 | FITC标记的Rho GTP酶激活蛋白36抗体 |
别 名 | Hypothetical Protein FLJ30058; Arhgap36; FLJ30058; hypothetical protein FLJ30058; Hypothetical protein LOC158763; OTTHUMP00000024023; OTTHUMP00000024024; OTTHUMP00000024026; Putative Rho GTPase activating protein FLJ46335; RHG36_HUMAN; Rho GTPase-activating protein 36; RP13 102H20.1; RP13-102H20.1. |
规格价格 | 100ul/2980元 购买 大包装/询价 |
说 明 书 | 100ul |
研究领域 | 细胞生物 免疫学 信号转导 G蛋白信号 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, Mouse, Rat, |
产品应用 | ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 57kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ARHGAP36 |
亚 型 | IgG |
纯化方法 | affinity purified by Protein A |
储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
产品介绍 | background: ARHGAP36 is a 547 amino acid protein that contains one Rho-GAP domain. Conserved in chimpanzee, dog, cow, mouse and rat, ARHGAP36 exists as five alternatively spliced isoforms and is encoded by a gene that maps to human chromosome Xq26.1. Chromosome X consists of nearly 153 million base pairs encoding approximately 1,000 genes. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are X chromosome-linked conditions that affect males more frequently because males carry a single X chromosome. Function: GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state. Similarity: Contains 1 Rho-GAP domain. Database links: Entrez Gene: 158763 Human SwissProt: Q6ZRI8 Human Unigene: 22905 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
ARHGAP36是一个含有547个Rho GAP结构域的蛋白质。ARHGAP36在黑猩猩、狗、奶牛、小鼠和大鼠中保存,作为五个可选择的剪接异构体存在,并且由映射到人类染色体Xq26.1的基因编码。X染色体由近1亿5300万个碱基对组成,编码约1000个基因。X染色体Y染色体的一个以上拷贝引起Krimelelter综合征。单拷贝X导致Turnter综合征。在Y染色体缺失的情况下,X染色体的2个拷贝被称为三重X综合征。色盲、血友病和杜氏肌营养不良是X染色体连锁疾病,由于男性携带单个X染色体,因此更频繁地影响男性。