產(chǎn)品編號(hào) | bs-16123R |
英文名稱 | ZNF474 Rabbit pAb |
中文名稱 | 鋅指蛋白蛋白474抗體 |
別 名 | FLJ32921Testis specific zinc finger protein; Testis-specific zinc finger protein; TSZFP; Zfp474; Zinc finger protein 474; ZN474_HUMAN; ZNF474. |
研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) 鋅指蛋白 |
抗體來(lái)源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Mouse (predicted: Human,Rat,Pig,Dog,Horse) |
產(chǎn)品應(yīng)用 | WB=1:500-2000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理論分子量 | 40 kDa |
檢測(cè)分子量 | |
細(xì)胞定位 | 細(xì)胞核 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ZNF474: 101-200/364 |
亞 型 | |
純化方法 | affinity purified by Protein A |
緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
保存條件 | Shipped at 4℃. Store at -20℃ 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. |
PubMed | PubMed |
產(chǎn)品介紹 |
ZNF474 is a 364 amino acid protein containing one C2H2-type zinc fingers. The gene encoding ZNF474 localizes to chromosome 5 which contains 181 million base pairs and comprises nearly 6% of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. Similarity: Contains 1 C2H2-type zinc finger. SWISS: Q6S9Z5 Gene ID: 133923 Database links: Entrez Gene: 133923 Human SwissProt: Q6S9Z5 Human Unigene: 646680 Human |
產(chǎn)品圖片 | |
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