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    首頁>>免疫學>>一抗>>過氧化氫誘導轉錄蛋白1抗體
    過氧化氫誘導轉錄蛋白1抗體
    • 產品貨號:
      BN41399R
    • 中文名稱:
      過氧化氫誘導轉錄蛋白1抗體
    • 英文名稱:
      Rabbit anti-C20orf111 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規(guī)格

      售價

      備注

    • BN41399R-100ul

      100ul

      ¥2360.00

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

    • BN41399R-200ul

      200ul

      ¥3490.00

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

    產品描述

    英文名稱C20orf111
    中文名稱過氧化氫誘導轉錄蛋白1抗體
    別    名Chromosome 20 open reading frame 111; CT111_HUMAN; HSPC207; Oxidative stress responsive 1; Perit1; Peroxide inducible transcript 1; Uncharacterized protein C20orf111.  
    研究領域細胞生物  免疫學  發(fā)育生物學  神經生物學  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Human, Mouse,  (predicted: Rat, Chicken, Dog, Pig, Cow, Rabbit, Zebrafish, Sheep, )
    產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=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32 kDa
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human C20orf111:1-100/292 
    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Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf111 gene product has been provisionally designated C20orf111 pending further characterization.

    SWISS:
    Q9NX31

    Gene ID:
    51526

    Database links:

    Entrez Gene: 51526 Human

    SwissProt: Q9NX31 Human

    SwissProt: Q9D722 Mouse

    Unigene: 75798 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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