DsbA Monoclonal Antibody, 50ul sgRNA Library Construction This gene is expressed predominantly

This gene is expressed predominantly in T-cells

Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2)

which required for microtubule nucleation at the centrosome

Gene Ontology (GO) annotations related to NFRKB include protease binding

known as the paired box

DsbA Monoclonal Antibody, 50ul sgRNA Library Construction This gene is expressed predominantlyP0AEG4 periplasmic protein disulfide isomerase I(dsbA) Escherichia coli str. K 12 substr. MG1655 function: Required for disulfide bond formation in some periplasmic proteins such as phoA or ompA. Acts by transferring its disulfide bond to other proteins and is reduced in the process. DsbA is reoxidized by dsbB. It is required for pilus biogenesis.,similarity: Belongs to the thioredoxin family. DsbA subfamily.,similarity: Contains 1 thioredoxin domain.,