<legend id="oozfl"></legend>
    <strike id="oozfl"></strike>
    掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
      
    客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
    產品中心-北京博奧森生物技術有限公司
    首頁 > 產品中心 > 標記一抗 > 產品信息
    Rabbit Anti-ARHGAP36/Gold Conjugated antibody (bs-18116R-Gold)
    訂購熱線:400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
    技術支持:techsupport@bioss.com.cn
    說 明 書: 100ul(10nm  15nm  35nm
    100ul/2980.00元
    大包裝/詢價
    產品編號 bs-18116R-Gold
    英文名稱 Rabbit Anti-ARHGAP36/Gold Conjugated antibody
    中文名稱 膠體金標記的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.  
    規格價格 100ul/2980元 購買        大包裝/詢價
    說 明 書 100ul(10nm  15nm  35nm
    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
    交叉反應 (predicted: Human, Mouse, Rat, )
    產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
    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 0.4mg/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 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
    保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
    產品介紹 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.
    版權所有 2004-2026 www.radiasunchina.com 北京博奧森生物技術有限公司
    通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
    通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
    京ICP備05066980號-1         京公網安備110107000727號
    国产剧情演绎系列丝袜高跟|一级毛片av性爱黄色网站|欧美三级午夜理伦三级|国产av巨作情欲放纵|亚洲 欧美 中文 日韩aⅴ

    <legend id="oozfl"></legend>
    <strike id="oozfl"></strike>