CHSTB Polyclonal Antibody, 50ul Miscellaneous a disorder characterized by urinary

a disorder characterized by urinary salt wasting

Mutations in this gene may be associated with a range of autoimmune disorders including Type 1 Diabetes

Binds to neuroligins NLGN1

MAP kinases play a significant role in many biological processes

mismatch repair system component forms heterodimers with the gene product of the mutL homolog 1 (MLH1) gene to form the MutL-alpha heterodimer

CHSTB Polyclonal Antibody, 50ul Miscellaneous a disorder characterized by urinaryThe protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of the N acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage, and is distributed on the surfaces of many cells and extracellular matrices. A chromosomal translocation involving this gene and IgH, t(12;