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Anti-C2CD4C/NLF3限局性核因子3抗体

点击次数:281发布时间:2012/12/26 8:18:16

Anti-C2CD4C/NLF3限局性核因子3抗体

更新日期:2024/9/5 14:43:40

所 在 地:其它

产品型号:BY-9989R

简单介绍:本公司经销C2CD4C/NLF3,限局性核因子3抗体,克隆类型为polyclonal,宿主来源是Rabbit,C2CD4C/NLF3限局性核因子3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C2CD4C/NLF3,限局性核因子3抗体,克隆类型为polyclonal,宿主来源是Rabbit,C2CD4C/NLF3限局性核因子3抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9989R
英文名称:Anti-C2CD4C/NLF3
中文名称:限局性核因子3抗体
其他名称:KIAA1957;C2 calcium-dependent domain-containing protein 4C;C2C4C_HUMAN;C2CD4C;NLF3;Nuclear-localized factor 3;Protein FAM148C.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 45kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat
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 Fc Alpha 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 FAM148C gene product has been provisionally designated FAM148C pending further characterization.

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