| 產(chǎn)品編號(hào) | bs-18116R-RBITC |
| 英文名稱 | Rabbit Anti-ARHGAP36/RBITC Conjugated antibody |
| 中文名稱 | 羅丹明（RBITC）標(biāo)記的Rho GTP酶激活蛋白36抗體 |
| 別 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. |
| 規(guī)格價(jià)格 | 100ul/2980元 購(gòu)買 大包裝/詢價(jià) |
| 說(shuō) 明 書(shū) | 100ul |
| 研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) 信號(hào)轉(zhuǎn)導(dǎo) G蛋白信號(hào) |
| 抗體來(lái)源 | Rabbit |
| 克隆類型 | Polyclonal |
| 交叉反應(yīng) | (predicted: Human, Mouse, Rat, ) |
| 產(chǎn)品應(yīng)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 狀 | Lyophilized or Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human ARHGAP36 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 儲(chǔ) 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存條件 | 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. |
| 產(chǎn)品介紹 |
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. |
