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产品展示

CXorf21X染色体开放阅读框21抗体

点击次数:239发布时间:2012/12/5 11:12:01

CXorf21X染色体开放阅读框21抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9552R

简单介绍:本公司经销CXorf21,X染色体开放阅读框21抗体,克隆类型为polyclonal,宿主来源是Rabbit,CXorf21X染色体开放阅读框21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CXorf21,X染色体开放阅读框21抗体,克隆类型为polyclonal,宿主来源是Rabbit,CXorf21X染色体开放阅读框21抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9552R
英文名称:Anti-CXorf21
中文名称:X染色体开放阅读框21抗体
其他名称:Chromosome X open reading frame 21;FLJ11577;Hypothetical protein LOC80231;Uncharacterized protein CXorf21.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 34kDa
纯化方法:affinity purified by Protein A
交叉反应:hu
产品介绍:The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.

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