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C17orf4917号染色体开放阅读框49抗体

点击次数:194发布时间:2012/12/5 10:42:18

C17orf4917号染色体开放阅读框49抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9640R

简单介绍:本公司经销C17orf49,17号染色体开放阅读框49抗体,克隆类型为polyclonal,宿主来源是Rabbit,C17orf4917号染色体开放阅读框49抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

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本公司经销C17orf49,17号染色体开放阅读框49抗体,克隆类型为polyclonal,宿主来源是Rabbit,C17orf4917号染色体开放阅读框49抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9640R
英文名称:Anti-C17orf49
中文名称:17号染色体开放阅读框49抗体
其他名称:Bap18;BAP18_HUMAN;BPTF-associated protein of 18 kDa;Chromatin complexes subunit BAP18;Chromosome 17 open reading frame 49;Hypothetical protein LOC124944;MGC49942;Uncharacterized potential DNA binding protein C17orf49.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 18kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat, cow, dog, zebrafish
产品介绍:C17orf49 is a 172 amino acid protein that is encoded by a gene mapping to human chromosome 17. Chromosome 17 makes up over 2.5% of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.Subcellular Location : Nucleus.

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