IGSF4D Polyclonal Antibody, 20ul DNA Libraries Synthesis Defects in GRK1 are known

Defects in GRK1 are known to cause Oguchi disease 2 (also known as stationary night blindness Oguchi type-2)

this protein contains an SH2 domain flanked by two SH3 domains

Our specialized services include oligonucleotides (which can be modified with special bases)

GAPs stimulate the intrinsic GTP hydrolysis of small G proteins

A domain at its N-terminus can also interact with the poly(A)-binding protein

IGSF4D Polyclonal Antibody, 20ul DNA Libraries Synthesis Defects in GRK1 are knownCADM2 encodes a member of the synaptic cell adhesion molecule 1 (SynCAM) family which belongs to the immunoglobulin (Ig) superfamily. Cell adhesion molecule 2 has three Ig like domains and a cytosolic protein 4. 1 binding site near the C terminus. Proteins belonging to the protein 4. family crosslink spectrin and interact with other cytoskeletal proteins. Multiple transcript variants encoding different isoforms have been found for this gene.