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

C7orf76, DSS1, ECD, PSMD15, SHFD1, SHFM1, SHSF1, Shfdg1, 26S proteasome complex subunit SEM1, 26S proteasome complex subunit DSS1, SEM1 26S proteasome complex subunit, deleted in split hand/split foot protein 1, deleted in split-hand/split-foot 1, 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