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10號(hào)染色體開(kāi)放閱讀框47抗體
AK18547
C10orf47
Rabbit
Mouse,Rat (predicted: Human,Pig,Horse,Rabbit,Sheep)
WB,ELISA
多克隆
貨號(hào) 純度 規(guī)格 目錄價(jià) 會(huì)員價(jià) 庫(kù)存 數(shù)量 購(gòu)買
AK18547-50ul 50ul 50ul ¥1380.00 登錄查看
AK18547-100ul 100ul 100ul ¥2380.00 登錄查看
AK18547-200ul 200ul 200ul ¥3480.00 登錄查看
產(chǎn)品詳情

公司產(chǎn)品僅供科研研究實(shí)驗(yàn),不得用于臨床!

商品詳情:

英文名稱:C10orf47

中文名稱:10號(hào)染色體開(kāi)放閱讀框47抗體

   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(lái)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.

理論分子量;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

   狀;Liquid

   度;1mg/ml

原;KLH conjugated synthetic peptide derived from human C10orf47: 351-435/435

   型;IgG

純化方法;affinity purified by Protein A

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.

注意事項(xiàng);This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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.

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