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Anti-C12ORF54抗体,12号染色体开放阅读框54抗体科研

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“Anti-C12ORF54抗体,12号染色体开放阅读框54抗体科研“我公司拥有*的细胞服务技术，*的仪器设备和专业的ELISA检测试剂盒、生物索标记、荧光索标记、酶标记等，广泛用于多种分析研究与技术测定。咨询，我们将竭诚为你服务！

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Anti-C12ORF54抗体,12号染色体开放阅读框54抗体科研产品介绍：

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 C12orf54 gene product has been provisionally designated C12orf54 pending further characterization.

与“Anti-C12ORF54抗体,12号染色体开放阅读框54抗体科研"有关的产品：

细胞核因子/k基因结合核因子抗体 Anti-NFKB p65
alpha 1肾上腺素能受体B抗体 Anti-ADRA1B
高分子量神经丝蛋白抗体 Anti-NF-H/Neurofilament H/Neurofilament 200/NF200
DNA损伤关卡蛋白1抗体 Anti-NFBD1/MDC1
NFKB激活蛋白抗体 Anti-NKAP
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产品详情：
产品编号：HRK-9952R
产品规格: 0.1ml/0.2ml
产品别名：MGC35033; C12orf54; Chromosome 12 open reading frame 54; CL054_HUMAN; HSD 29; HSD 30; HSD29; Uncharacterized protein C12orf54
产品价格：询价(电询或客服)
产品用途：科研实验
贮存：贮存于-20℃.

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