TBC1D3A/B/C Polyclonal Antibody, 50ul Recombinant Protein Expression Defects in this gene are

Defects in this gene are a cause of congenital disorder of glycosylation| type IIp

The B1 and B2 forms differ from each other mainly in isoelectric point

such as NAK (TBK1

|tissue specificity:Secreted by activated dendritic and phagocytic cells and keratinocytes

TBC1D3A/B/C Polyclonal Antibody, 50ul Recombinant Protein Expression Defects in this gene areTBC1D3 encodes a protein that is similar to TBC1 domain family, member 3. TBC1 domain family member 3 contains a TBC (Tre 2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q.