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CRCT1富含半胱氨酸C端蛋白1抗体

点击次数:347发布时间:2012/12/3 22:05:16

CRCT1富含半胱氨酸C端蛋白1抗体

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-9956R

简单介绍:本公司经销CRCT1,富含半胱氨酸C端蛋白1抗体,克隆类型为polyclonal,宿主来源是Rabbit,CRCT1富含半胱氨酸C端蛋白1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CRCT1,富含半胱氨酸C端蛋白1抗体,克隆类型为polyclonal,宿主来源是Rabbit,CRCT1富含半胱氨酸C端蛋白1抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-9956R
英文名称:Anti-CRCT1
中文名称:富含半胱氨酸C端蛋白1抗体
其他名称:C1orf42;CRCT1;CRCT 1;CRCT-1;CRCT1_HUMAN;Cysteine rich C terminal 1;Cysteine-rich C-terminal protein 1;NICE 1;NICE1;NICE-1;Protein NICE-1.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 10kDa
纯化方法:affinity purified by Protein A
交叉反应:hu
产品介绍:Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

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