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C9ORF469号染色体开放阅读框46抗体

点击次数:144发布时间:2012/12/5 11:10:17

C9ORF469号染色体开放阅读框46抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9489R

简单介绍:本公司经销C9ORF46,9号染色体开放阅读框46抗体,克隆类型为polyclonal,宿主来源是Rabbit,C9ORF469号染色体开放阅读框46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C9ORF46,9号染色体开放阅读框46抗体,克隆类型为polyclonal,宿主来源是Rabbit,C9ORF469号染色体开放阅读框46抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9489R
英文名称:Anti-C9ORF46
中文名称:9号染色体开放阅读框46抗体
其他名称:FLJ14688;AD025;Chromosome 9 open reading frame 46;FLJ39176;Hypothetical protein LOC55848;MDS030;transmembrane protein C9orf46;Uncharacterized hematopoietic stem/progenitor cells protein MDS030.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 17kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, rat, mo, dog
产品介绍:C9orf46 is a 147 amino acid transmembrane protein. The gene encoding C9orf46 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered 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. Subcellular Location : Membrane; Multi pass membrane protein

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