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C11orf7111号染色体开放阅读框71抗体

点击次数:325发布时间:2012/12/3 22:18:54

C11orf7111号染色体开放阅读框71抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9941R

简单介绍:本公司经销C11orf71,11号染色体开放阅读框71抗体,克隆类型为polyclonal,宿主来源是Rabbit,C11orf7111号染色体开放阅读框71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C11orf71,11号染色体开放阅读框71抗体,克隆类型为polyclonal,宿主来源是Rabbit,C11orf7111号染色体开放阅读框71抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9941R
英文名称:Anti-C11orf71
中文名称:11号染色体开放阅读框71抗体
其他名称:C11orf71 chromosome 11 open reading frame 71;CK071_HUMAN;FLJ20010;Gm5617;hypothetical protein LOC54494;Uncharacterized protein C11orf71.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 13kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo
产品介绍:C11orf71, also known as FLJ20010, 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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