簡要描述:11號(hào)染色體開放閱讀框74抗體免 疫 原;KLH conjugated synthetic peptide derived from human C11orf74: 111-210/221
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11號(hào)染色體開放閱讀框74抗體
產(chǎn)品名稱 | 英文名稱 | 貨號(hào) |
11號(hào)染色體開放閱讀框74抗體 | C11orf74 | GOY-01K4262 |
商品屬性:
英文名稱: C11orf74
中文名:11號(hào)染色體開放閱讀框74抗體
別 名;Chromosome 11 open reading frame 74; FLJ38678; HEPIS; Hypothetical protein LOC119710; Protein HEPIS; CK074_HUMAN.
研究領(lǐng)域;心血管 細(xì)胞生物 免疫學(xué) 神經(jīng)生物學(xué)
抗體來源;Rabbit
克隆類型;Polyclonal
交叉反應(yīng);(predicted: Human, Mouse, Rat, )
產(chǎn)品應(yīng)用;WB=1:500-2000 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;25kDa
細(xì)胞定位;細(xì)胞核 細(xì)胞漿 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 C11orf74: 111-210/221
亞 型;IgG
純化方法;affinity purified by Protein A
緩 沖 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:
C11orf74, also known as FLJ38678, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. |
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