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商品详情：
英文名称：DSS1
中文名称：先天性裂手/裂足畸形相关蛋白DSS1抗体
别 名:26S proteasome complex subunit DSS1; Deleted in split hand/split foot 1; Deleted in Split-Hand/Split-Foot 1 region; ECD; SEM1; SHFD1; DSS1_HUMAN; SHFM1; SHSF1; PSMD15; Shfdg1; C7orf76; Split hand/foot deleted protein 1; Split hand/foot malformation (ectrodactyly) type 1; Split hand/foot malformation type 1 protein.
研究领域:细胞生物 发育生物学 细胞周期蛋白 泛素
抗体来源:Rabbit
克隆类型:Polyclonal
交叉反应: Human, (predicted: Pig, Cow, Rabbit, )
产品应用:ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量:8.3kDa
细胞定位:细胞核 细胞浆
性 状:Liquid
浓 度:1mg/ml
免 疫 原:KLH conjugated synthetic peptide derived from human DSS1: 1-70/70
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
先天性裂手/裂足畸形相关蛋白DSS1抗体注意事项:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Function:
The gene for DSS1 has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. DSS1 has been proposed to be a candidate 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.
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