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聯(lián)系我時,請告知來自 環(huán)保在線博研生物強烈*“Anti-C12orf72抗體,12號染色體開放閱讀框72抗體介紹",品質(zhì)保障,*,提供,實驗無結(jié)果可免費退換?。?/p>
產(chǎn)品介紹:
產(chǎn)品名稱:Anti-C12orf72抗體,12號染色體開放閱讀框72抗體介紹
產(chǎn)品編號:BYK-18117R
英文名稱 C12orf72
中文名稱 12號染色體開放閱讀框72抗體
別 名 hypothetical protein LOC254013; C12orf72; Chromosome 12 open reading frame 72; MGC50559; UPF0516 protein C12orf72.
研究領(lǐng)域 細胞生物 免疫學
產(chǎn)品價格:詢價(電詢或客服)
抗體來源:本公司抗體有兔來源和鼠來源等
克隆類型:兔來源為多抗,鼠來源為單抗
產(chǎn)品類型:一抗
產(chǎn)品用途:科研實驗
性 狀: Lyophilized or Liquid
濃 度: 1mg/1ml
亞 型: IgG
貯 存: 貯存于-20℃.
Anti-C12orf72抗體,12號染色體開放閱讀框72抗體介紹介紹:GTPase-activating proteins (GAPs) accelerate the intrinsic rate of GTP hydrolysis of Ras-related proteins, resulting in downregulation of their active form. ARHGAP36 (Rho GTPase activating protein 36) 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 approximay 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.
相關(guān)的標記有:Alexa Fluor 350 標記、Alexa Fluor 488 標記、Alexa Fluor 555 標記、Alexa Fluor 647 標記、AP標記、APC標記、Biotin標記、Cy3標記、Cy5標記、Cy5.5標記、Cy7標記、FITC標記、Gold標記、HRP標記、PE標記、PE-Cy3標記、PE-CY5標記、PE-CY5.5標記、PE-CY7標記、RBITC標記
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.
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