Anti-C1orf110抗体,1号染色体开放阅读框110抗体科研产品介绍：

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. The C1orf110 gene product has been provisionally designated C1orf110 pending further characterization. 

与“Anti-C1orf110抗体,1号染色体开放阅读框110抗体科研”有关的产品：

Anti-CD304/BDCA-4/NRP-1抗体说明书，神经纤毛蛋白-1抗体
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Anti-NT-4/NT-5抗体说明书，神经生长因子4/5抗体
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Anti-NTN抗体说明书，神经生长因子抗体
Anti-Ntn1抗体说明书，轴突导向因子1抗体

产品详情：
产品编号：HRK-15006R
产品规格: 0.1ml/0.2ml
产品别名：Chromosome 1 open reading frame 110; Coiled coil domain containing protein C1orf110; FLJ41579; Hypothetical protein LOC339512; MGC48998; RP11-331H2.2; CA110_HUMAN
产品价格：询价(电询或客服)
产品用途：科研实验
贮 存：   贮存于-20℃.

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