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Anti-C9orf1529号染色体开放阅读框152抗体

点击次数:198发布时间:2012/12/26 8:24:56

Anti-C9orf1529号染色体开放阅读框152抗体

更新日期:2024/9/5 14:43:40

所 在 地:其它

产品型号:BY-9497R

简单介绍:本公司经销C9orf152,9号染色体开放阅读框152抗体,克隆类型为polyclonal,宿主来源是Rabbit,C9orf1529号染色体开放阅读框152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C9orf152,9号染色体开放阅读框152抗体,克隆类型为polyclonal,宿主来源是Rabbit,C9orf1529号染色体开放阅读框152抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9497R
英文名称:Anti-C9orf152
中文名称:9号染色体开放阅读框152抗体
其他名称:Chromosome 9 open reading frame 152;Hypothetical protein LOC401546;Uncharacterized protein C9orf152.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 26kDa
纯化方法:affinity purified by Protein A
交叉反应:hu
产品介绍:C9orf152 is a 239 amino acid protein encoded by a gene that maps to human chromosome 9q31.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

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