Anti-C12ORF61抗體*,12號染色體開放閱讀框61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 C12orf61 gene product has been provisionally designated C12orf61 pending further characterization.

與“Anti-C12ORF61抗體*,12號染色體開放閱讀框61抗體科研"有關的產品:
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活化T細胞核因子1蛋白抗體 Anti-NFATc1/NFAT2
黑素皮質素受體4抗體 Anti-MC4 Receptor/MC4-R
突觸泡蛋白2C抗體 Anti-SV2C
產品詳情:
產品編號:HRK-9953R
產品規格: 0.1ml/0.2ml
產品別名:C12orf61; CL061_HUMAN; Putative uncharacterized protein C12orf61
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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