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C19orf2419号染色体开放阅读框24抗体

点击次数:204发布时间:2012/12/3 22:04:37

C19orf2419号染色体开放阅读框24抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9679R

简单介绍:本公司经销C19orf24,19号染色体开放阅读框24抗体,克隆类型为polyclonal,宿主来源是Rabbit,C19orf2419号染色体开放阅读框24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C19orf24,19号染色体开放阅读框24抗体,克隆类型为polyclonal,宿主来源是Rabbit,C19orf2419号染色体开放阅读框24抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9679R
英文名称:Anti-C19orf24
中文名称:19号染色体开放阅读框24抗体
其他名称:C19orf24;Chromosome 19 open reading frame 24;CS024_HUMAN;FLJ20640;Hypothetical protein LOC55009;Uncharacterized membrane protein C19orf24.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 14kDa
纯化方法:affinity purified by Protein A
交叉反应:hu
产品介绍:Consisting of around 63 million bases with over 1,400 genes, chromosome 19 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. The C19orf24 gene product has been provisionally designated C19orf24 pending further characterization.Subcellular Location : Membrane.

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