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C19orf4519号染色体开放阅读框45抗体

点击次数:212发布时间:2012/12/3 22:02:24

C19orf4519号染色体开放阅读框45抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9681R

简单介绍:本公司经销C19orf45,19号染色体开放阅读框45抗体,克隆类型为polyclonal,宿主来源是Rabbit,C19orf4519号染色体开放阅读框45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C19orf45,19号染色体开放阅读框45抗体,克隆类型为polyclonal,宿主来源是Rabbit,C19orf4519号染色体开放阅读框45抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9681R
英文名称:Anti-C19orf45
中文名称:19号染色体开放阅读框45抗体
其他名称:chromosome 19 open reading frame 45;C19orf45;CS045_HUMAN;FLJ35784;FLJ56642;hypothetical protein LOC374877;Uncharacterized protein C19orf45.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 57kDa
纯化方法:affinity purified by Protein A
交叉反应:hu
产品介绍:C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

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