产品展示
C18orf5618号染色体开放阅读框56抗体
点击次数：193发布时间：2012/12/3 22:03:35
更新日期：2024/9/5 14:43:01
所 在 地：中国大陆
产品型号：BY-9675R
优质供应
详细内容
货号：BY-9675R
英文名称：Anti-C18orf56
中文名称：18号染色体开放阅读框56抗体
其他名称：Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations ａnd breathing difficulty. Translocation between chromosome 18 ａnd 14 is the most common translocation in cancers, ａnd occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia ａnd erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 ａnd Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
抗体来源：Rabbit
克隆类型：polyclonal
蛋白分子量：predicted molecular weight: 13kDa
纯化方法：affinity purified by Protein A
交叉反应：hu
产品介绍：Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations ａnd breathing difficulty. Translocation between chromosome 18 ａnd 14 is the most common translocation in cancers, ａnd occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia ａnd erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 ａnd Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
