Human 26S proteasome complex subunit DSS1 ELISA Kit | SHFM1 elisa kit
Human 26S proteasome complex subunit DSS1 ELISA Kit
NCBI and Uniprot Product Information
NCBI Description
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]
Uniprot Description
SHFM1: Subunit of the 26S proteasome which plays a role in ubiquitin-dependent proteolysis. Belongs to the DSS1/SEM1 family.
Protein type: DNA repair, damage; Proteasome complex; Protease
Chromosomal Location of Human Ortholog: 7q21.3
Cellular Component: proteasome complex; integrator complex
Molecular Function: protein binding
Biological Process: double-strand break repair via homologous recombination
Disease: Split-hand/foot Malformation 1
Research Articles on SHFM1
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Product Notes
The Human SHFM1 shfm1 (Catalog #AAA7217018) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA7217018 ELISA Kit recognizes Human SHFM1. It is sometimes possible for the material contained within the vial of "26S proteasome complex subunit DSS1, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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