DSS1 antibody, C-term

GeneTex

DSS1 antibody, C-term

9

ImmunoFluorescence, ImmunoCytoChemistry

Research Use Only

Polyclonal

0.50 mg/ml

Unconjugated

SEM1

SEM1 26S proteasome subunit

26S proteasome complex subunit DSS1; 26S proteasome complex subunit SEM1; C7orf76; deleted in split hand/split foot protein 1; deleted in split-hand/split-foot 1; DSS1; ECD; PSMD15; SEM1 26S proteasome complex subunit; SHFD1; Shfdg1; SHFM1; SHSF1; split hand/foot deleted protein 1; split hand/foot malformation (ectrodactyly) type 1; split hand/foot malformation type 1 protein

Goat

IgG

26S proteasome complex subunit SEM1

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]

-20°C or -80°C,2°C to 8°C

12352203