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C11orf6511号染色体开放阅读框65抗体

点击次数:245发布时间:2012/12/3 22:18:33

C11orf6511号染色体开放阅读框65抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9940R

简单介绍:本公司经销C11orf65,11号染色体开放阅读框65抗体,克隆类型为polyclonal,宿主来源是Rabbit,C11orf6511号染色体开放阅读框65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C11orf65,11号染色体开放阅读框65抗体,克隆类型为polyclonal,宿主来源是Rabbit,C11orf6511号染色体开放阅读框65抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9940R
英文名称:Anti-C11orf65
中文名称:11号染色体开放阅读框65抗体
其他名称:Chromosome 11 open reading frame 65;Hypothetical protein LOC160140.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 37kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat
产品介绍:C11orf65, also known as MGC33948, is a 313 amino acid protein that 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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