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RXR Alpha/RXRA/Retinoid X receptor核受体RXRα抗体

产品信息
本公司经销RXR Alpha/RXRA/Retinoid X receptor,核受体RXRα抗体,克隆类型为polyclonal,宿主来源是Rabbit,RXR Alpha/RXRA/Retinoid X receptor核受体RXRα抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!
本公司经销RXR Alpha/RXRA/Retinoid X receptor,核受体RXRα抗体,克隆类型为polyclonal,宿主来源是Rabbit,RXR Alpha/RXRA/Retinoid X receptor核受体RXRα抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-1379R
英文名称:Anti-RXR Alpha/RXRA/Retinoid X receptor
中文名称:核受体RXRα抗体
其他名称:名Retinoid X receptor alpha; FLJ16020; FLJ16733; MGC102720; NR2B1; Retinoic acid receptor RXR alpha; RXR alpha1; RXRalpha1; retinoid-X receptor alpha.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 51kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, rat, mo
产品介绍:The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.
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