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華瑞科研網-ELISA試劑盒
華瑞科研網-ELISA試劑盒
“Anti-C12ORF24抗體,12號染色體開放閱讀框24抗體科研“我公司擁有*的細胞服務技術，*的儀器設備和專業的ELISA檢測試劑盒、生物索標記、熒光索標記、酶標記等，廣泛用于多種分析研究與技術測定。咨詢，我們將竭誠為你服務！
Anti-C12ORF24抗體,12號染色體開放閱讀框24抗體科研產品介紹：
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.
與“Anti-C12ORF24抗體,12號染色體開放閱讀框24抗體科研"有關的產品：
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Anti-MTA1(Metastasis-associated 1) 腫瘤轉移相關蛋白1抗體
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產品詳情：
產品編號：HRK-9945R
產品規格: 0.1ml/0.2ml
產品別名：Chromosome 12 open reading frame 24; HSU79274; Hypothetical protein LOC29902; Protein predicted by clone 23733; F216A_HUMAN
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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