Anti-C2orf39抗體,2號染色體開放閱讀框39抗體科研產品介紹:
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximay 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial omeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf39 gene product has been provisionally designated C2orf39 pending further characterization.

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產品詳情:
產品編號:HRK-15149R
產品規格: 0.1ml/0.2ml
產品別名:CC164_HUMAN; CCDC164; Coiled-coil domain-containing protein 164
產品價格:詢價(電詢或客服)
產品用途:科研實驗
貯 存: 貯存于-20℃.
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