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    卷曲螺旋結(jié)構(gòu)域蛋白125抗體
    • 產(chǎn)品貨號(hào):
      BN41237R
    • 中文名稱:
      卷曲螺旋結(jié)構(gòu)域蛋白125抗體
    • 英文名稱:
      Rabbit anti-CCDC125 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號(hào)

      產(chǎn)品規(guī)格

      售價(jià)

      備注

    • BN41237R-100ul

      100ul

      ¥2360.00

      交叉反應(yīng):Mouse(predicted:Human,Rat,Pig,Cow,Sheep) 推薦應(yīng)用:WB,IHC-P,IHC-F,IF,ELISA

    • BN41237R-200ul

      200ul

      ¥3490.00

      交叉反應(yīng):Mouse(predicted:Human,Rat,Pig,Cow,Sheep) 推薦應(yīng)用:WB,IHC-P,IHC-F,IF,ELISA

    產(chǎn)品描述

    英文名稱CCDC125
    中文名稱卷曲螺旋結(jié)構(gòu)域蛋白125抗體
    別    名CC125_HUMAN; CCDC125; Coiled-coil domain-containing protein 125; KENAE;y Protein kenae.  
    研究領(lǐng)域細(xì)胞生物  免疫學(xué)  
    抗體來(lái)源Rabbit
    克隆類型Polyclonal
    交叉反應(yīng)Mouse,  (predicted: Human, Rat, Pig, Cow, Sheep, )
    產(chǎn)品應(yīng)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(fù))
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量56kDa
    細(xì)胞定位細(xì)胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human CCDC125:151-250/511 
    亞    型IgG
    純化方法affinity purified by Protein A
    儲(chǔ) 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(chǎn)品介紹CCDC125, also known as KENAE, is a 511 amino acid protein expressed as two isoforms produced by alternative splicing and encoded by a gene mapping to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

    Function:
    May be involved in the regulation of cell migration.

    Subcellular Location:
    Cytoplasm.

    SWISS:
    Q86Z20

    Gene ID:
    202243

    Database links:
    UniProtKB/Swiss-Prot: Q86Z20.2

    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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