Anti-C1orf76抗體,神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體科研產(chǎn)品介紹:
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 C1orf76 gene product has been provisionally designated C1orf76 pending further characterization.

與“Anti-C1orf76抗體,神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體科研"有關(guān)的產(chǎn)品:
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產(chǎn)品詳情:
產(chǎn)品編號:HRK-11711R
產(chǎn)品規(guī)格: 0.1ml/0.2ml
產(chǎn)品別名:C1orf76; NDSP; FAM163A; Chromosome 1 open reading frame 76; F163A_HUMAN; Fam163a; hypothetical protein MGC16664; NDSP; Neuroblastoma derived secretory protein; Neuroblastoma-derived secretory protein; Protein FAM163A
產(chǎn)品價格:詢價(電詢或客服)
產(chǎn)品用途:科研實驗
貯 存: 貯存于-20℃.
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