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    最近搜索:細胞培養 微生物學 分子生物 生物化學
    首頁>>免疫學>>一抗>>10號染色體開放閱讀框47抗體
    10號染色體開放閱讀框47抗體
    • 產品貨號:
      BN41406R
    • 中文名稱:
      10號染色體開放閱讀框47抗體
    • 英文名稱:
      Rabbit anti-C10orf47 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN41406R-100ul

      100ul

      ¥2360.00

      交叉反應:Mouse,Rat(predicted:Human,Pig,Horse,Rabbit,Sheep) 推薦應用:WB,ELISA

    • BN41406R-200ul

      200ul

      ¥3490.00

      交叉反應:Mouse,Rat(predicted:Human,Pig,Horse,Rabbit,Sheep) 推薦應用:WB,ELISA

    產品描述

    英文名稱C10orf47
    中文名稱10號染色體開放閱讀框47抗體
    別    名C10orf47; Chromosome 10 open reading frame 47; CJ047_HUMAN; Hypothetical protein LOC254427; MGC35403; Uncharacterized protein C10orf47.  
    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, Rat,  (predicted: Human, Pig, Horse, Rabbit, Sheep, )
    產品應用WB=1:500-2000 ELISA=1:5000-10000 
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量46kDa
    細胞定位細胞核 細胞漿 細胞膜 細胞外基質 分泌型蛋白 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human C10orf47:351-435/435 
    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C10orf47 is a 435 amino acid protein that exists as two alternatively spliced isoforms that are encoded by a gene located on human chromosome 10. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

    SWISS:
    Q86WR7

    Gene ID:
    254427

    Database links:




    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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