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首頁>>免疫學(xué)>>一抗>>10號(hào)染色體開放閱讀框47抗體
10號(hào)染色體開放閱讀框47抗體
  • 產(chǎn)品貨號(hào):
    BN41406R
  • 中文名稱:
    10號(hào)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(hào)

    產(chǎn)品規(guī)格

    售價(jià)

    備注

  • BN41406R-100ul

    100ul

    ¥2360.00

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

  • BN41406R-200ul

    200ul

    ¥3490.00

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

產(chǎn)品描述

英文名稱C10orf47
中文名稱10號(hào)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(lǐng)域細(xì)胞生物  免疫學(xué)  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應(yīng)Mouse, Rat,  (predicted: Human, Pig, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)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(xì)胞定位細(xì)胞核 細(xì)胞漿 細(xì)胞膜 細(xì)胞外基質(zhì) 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(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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