SH2D1A rabbit monoclonal antibody package:100 μl Defects in this gene are

Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6)

this protein is ubiquitinated and is involved in the RAD6-dependent DNA repair pathway

Swissprot No Q9NX76 Gene Accession NP_060271 WB Predicted band size 20 kDa WB Positive control WB Recommended dilution 500-2000 IHC predicted cell location Predicted cell location: Cytoplasm IHC positive control Positive control: Human tonsil IHC Recommed dilution Recommended dilution: 50-100 Storage

75A 50/60Hz Power 30W Fuse 250V

This protein

SH2D1A rabbit monoclonal antibody package:100 μl Defects in this gene areSpecification Full name SH2D1A rabbit monoclonal antibody Alternative names 50 l 100 l Reactivity rabbit monoclonal Applications WB Host Rabbit Clone type rabbit monoclonal Target Background This gene encodes a protein that plays a major role in the bidirectional stimulation of T and B cells. This protein contains an SH2 domain and a short tail. It associates with the signaling lymphocyte activation molecule, thereby acting as an inhibitor of this