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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total DSS1.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 26S proteasome complex subunit DSS1; deleted in split hand/split foot protein 1; deleted in split hand/split foot protein 1 homolog; deleted in split-hand/split-foot 1; Method: conceptual translation supplied by author.; SEM1 26S proteasome complex subunit; SEM1, 26S proteasome complex subunit; SHFM1; split hand/foot deleted gene 1; split hand/foot deleted protein 1; split hand/foot deleted protein 1 homolog; split hand/foot malformation (ectrodactyly) type 1; split hand/foot malformation type 1 protein; split hand/foot malformation type 1 protein homolog; unnamed protein product
基因别名: C7orf76; DSS1; ECD; PSMD15; SHFD1; Shfdg1; Shfg; SHFM1; SHSF1
UniProt ID: (Human) P60896, (Mouse) P60897
Entrez Gene ID: (Human) 7979, (Mouse) 20422, (Rat) 680532