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        ARHGAP36 Rabbit pAb (bs-18116R)  
        訂購熱線:400-901-9800
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        50ul/1180.00元
        100ul/1980.00元
        200ul/2800.00元
        大包裝/詢價
        產品編號 bs-18116R
        英文名稱 ARHGAP36 Rabbit pAb
        中文名稱 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.  
        研究領域 細胞生物  免疫學  信號轉導  G蛋白信號  
        抗體來源 Rabbit
        克隆類型 Polyclonal
        克 隆 號
        交叉反應 (predicted: Human,Mouse,Rat)
        產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
        not yet tested in other applications.
        optimal dilutions/concentrations should be determined by the end user.
        理論分子量 57 kDa
        檢測分子量
        細胞定位 細胞漿 細胞膜 
        性    狀 Liquid
        濃    度 1mg/ml
        免 疫 原 KLH conjugated synthetic peptide derived from human ARHGAP36: 351-450/547 
        亞    型 IgG
        純化方法 affinity purified by Protein A
        緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
        保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
        注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
        PubMed PubMed
        產品介紹 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.

        SWISS:
        Q6ZRI8

        Gene ID:
        158763

        Database links:

        Entrez Gene: 158763 Human

        SwissProt: Q6ZRI8 Human

        Unigene: 22905 Human



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