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    首頁>>免疫學>>一抗>>卷曲螺旋結構域蛋白7抗體
    卷曲螺旋結構域蛋白7抗體
    • 產品貨號:
      BN41292R
    • 中文名稱:
      卷曲螺旋結構域蛋白7抗體
    • 英文名稱:
      Rabbit anti-CCDC7 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN41292R-100ul

      100ul

      ¥2360.00

      交叉反應:Mouse(predicted:Human,Rat,Dog,Pig,Cow,Horse) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA

    • BN41292R-200ul

      200ul

      ¥3490.00

      交叉反應:Mouse(predicted:Human,Rat,Dog,Pig,Cow,Horse) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA

    產品描述

    英文名稱CCDC7
    中文名稱卷曲螺旋結構域蛋白7抗體
    別    名BioT2 A; BioT2 B; BioT2 C; CCDC 7; Coiled coil domain containing 7; Coiled coil domain containing protein 7; CCDC7_HUMAN.  
    研究領域細胞生物  免疫學  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Mouse,  (predicted: Human, Rat, Dog, Pig, Cow, Horse, )
    產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量56kDa
    細胞定位細胞核 細胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human CCDC7:155-250/486 
    亞    型IgG
    純化方法affinity purified by Protein A
    儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMedPubMed
    產品介紹The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. Some proteins that contain coil-coiled domains include c-jun, c-fos and tropomyosin. Coiled-coil domains consist of two or more ?helices packed together via interlacing side chains. CCDC7 (Coiled-coil domain-containing protein 7) is a 486 amino acid protein that contains a coiled-coil domain and is encoded by a gene that maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman抯 syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria. There are two isoforms of CCDC7 that are produced as a result of alternative splicing events.

    SWISS:
    Q96M83

    Gene ID:
    221016

    Database links:

    Entrez Gene: 221016 Human

    SwissProt: Q96M83 Human



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.


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