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    最近搜索:細胞培養(yǎng) 微生物學 分子生物 生物化學
    首頁>>免疫學>>一抗>>卷曲螺旋結(jié)構(gòu)域蛋白12抗體
    卷曲螺旋結(jié)構(gòu)域蛋白12抗體
    • 產(chǎn)品貨號:
      BN41302R
    • 中文名稱:
      卷曲螺旋結(jié)構(gòu)域蛋白12抗體
    • 英文名稱:
      Rabbit anti-CCDC12 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產(chǎn)品規(guī)格

      售價

      備注

    • BN41302R-100ul

      100ul

      ¥2360.00

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

    • BN41302R-200ul

      200ul

      ¥3490.00

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

    產(chǎn)品描述

    英文名稱CCDC12
    中文名稱卷曲螺旋結(jié)構(gòu)域蛋白12抗體
    別    名CCD12_HUMAN; CCDC12; Coiled coil domain containing 12; Coiled-coil domain-containing protein 12; FLJ39430; FLJ40801; MGC23918.  
    研究領(lǐng)域細胞生物  免疫學  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Human, Rat,  (predicted: Mouse, Dog, Pig, Cow, Horse, )
    產(chǎn)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19kDa
    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 CCDC12:19-120/166 
    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(chǎn)品介紹CCDC12, also known as FLJ39430, FLJ40801 or MGC23918, is a 166 amino acid protein encoded by a gene mapping to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

    SWISS:
    Q8WUD4

    Gene ID:
    151903

    Database links:

    Entrez Gene: 151903 Human

    Entrez Gene: 72654 Mouse

    Entrez Gene: 363151 Rat

    SwissProt: Q8WUD4 Human

    SwissProt: Q8R344 Mouse

    Unigene: 631918 Human



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