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華瑞科研網(wǎng)-ELISA試劑盒
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華瑞科研網(wǎng)-ELISA試劑盒
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廠商性質(zhì)生產(chǎn)商
所 在 地上海市
聯(lián)系方式：韓經(jīng)理查看聯(lián)系方式
更新時(shí)間：2018-04-14 07:47:34瀏覽次數(shù)：312次
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經(jīng)營(yíng)模式：生產(chǎn)廠家
商鋪產(chǎn)品：9992條
所在地區(qū)：上海上海市
聯(lián)系人：韓經(jīng)理 （銷(xiāo)售）
“Anti-C1orf100抗體,1號(hào)染色體開(kāi)放閱讀框100抗體科研“我公司擁有*的細(xì)胞服務(wù)技術(shù)，*的儀器設(shè)備和專(zhuān)業(yè)的ELISA檢測(cè)試劑盒、生物索標(biāo)記、熒光索標(biāo)記、酶標(biāo)記等，廣泛用于多種分析研究與技術(shù)測(cè)定。咨詢(xún)，我們將竭誠(chéng)為你服務(wù)！
Anti-C1orf100抗體,1號(hào)染色體開(kāi)放閱讀框100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 C1orf100 gene product has been provisionally designated C1orf100 pending further characterization.
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Anti-CD304/BDCA-4/NRP-1抗體說(shuō)明書(shū)，神經(jīng)纖毛蛋白-1抗體
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Anti-NTN抗體說(shuō)明書(shū)，神經(jīng)生長(zhǎng)因子抗體
Anti-Ntn1抗體說(shuō)明書(shū)，軸突導(dǎo)向因子1抗體
產(chǎn)品詳情：
產(chǎn)品編號(hào)：HRK-15000R
產(chǎn)品規(guī)格: 0.1ml/0.2ml
產(chǎn)品別名：C1orf100; CA100_HUMAN; Uncharacterized protein C1orf100
產(chǎn)品價(jià)格：詢(xún)價(jià)(電詢(xún)或客服)
產(chǎn)品用途：科研實(shí)驗(yàn)
貯 存： 貯存于-20℃.
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