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10號染色體開放閱讀框30抗體
AK18548
C10orf30
Rabbit
(predicted: Human,Mouse,Rat,Chicken,Cow,Horse,Rabbit,Sheep)
WB,IHC-P,IHC-F,IF,ELISA
多克隆
貨號 純度 規(guī)格 目錄價 會員價 庫存 數(shù)量 購買
AK18548-50ul 50ul 50ul ¥1380.00 登錄查看
AK18548-100ul 100ul 100ul ¥2380.00 登錄查看
AK18548-200ul 200ul 200ul ¥3480.00 登錄查看
產(chǎn)品詳情

公司產(chǎn)品僅供科研研究實驗,不得用于臨床!

商品詳情:

英文名稱:C10orf30

中文名稱:10號染色體開放閱讀框30抗體

   名;BEN domain-containing protein 7; BEND7; Chromosome 10 open reading frame 30; FLJ40283; MGC35247; BEND7_HUMAN.

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(yīng);(predicted: Human, Mouse, Rat, Chicken, Cow, Horse, Rabbit, 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=1:50-200 (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.

理論分子量;58kDa

細胞定位;細胞外基質(zhì) 分泌型蛋白

   狀;Liquid

   度;1mg/ml

原;KLH conjugated synthetic peptide derived from human C10orf30/BEND7: 251-350/519

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

產(chǎn)品介紹;BEND7 is a 519 amino acid protein that contains a BEN domain. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. BEND7 exists as three independently spiced isoforms and the gene that encodes BEND7 maps to chromosome 10p13. Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.

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