SC61B Polyclonal Antibody, 20ul Serum Mutations in THBD are a

Mutations in THBD are a cause of thromboembolic disease

0 kb in fetal lung and with one transcript of 8

PTM:It is not sure whether N-glycosylation is on Asn-165 and/or Asn-166

and tek/tie-2) whose expression is almost exclusively restricted to the endothelial cells

which phosphorylates multiple target proteins to promote transcriptional elongation

SC61B Polyclonal Antibody, 20ul Serum Mutations in THBD are aThe Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. Oligomers of the Sec61 complex form a transmembrane channel where proteins are translocated across and integrated into the ER membrane. This complex consists of three membrane proteins alpha, beta, and gamma. This gene encodes the beta subunit protein. The Sec61 subunits are also observed in the post ER compartment, suggesting