Split Hand/foot Malformation (Ectrodactyly) Type 1 ELISA试剂盒
(Split Hand/foot Malformation (Ectrodactyly) Type 1 (SHFM1))
The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008].
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
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| SHFM1 ELISA 试剂盒 | 小鼠 | – |
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| SHFM1 ELISA 试剂盒 | 人 | – |
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| SHFM1 ELISA 试剂盒 | Cow | – |
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