The following mannose-P-dolichol utilization defect 1 ELISA kits are useful research tools for the measurement of mannose-P-dolichol utilization defect 1 in biological samples. In humans this protein is encoded by the MPDU1 gene. This protein is reported to be required for normal utilization of mannose-dolichol phosphate (Dol-P-Man) in the synthesis of N-linked and O-linked oligosaccharides and GPI anchors. The canonical protein structure is reported to have an amino acid length of 247 residues, a mass of 26.6 kDa, and is a member of the MPDU1 (TC 2.A.43.3) protein family. Its subcellular location is known to be in the membrane. As many as 2 protein isoforms have been reported. The gene encoding this protein has been associated with the disease, Congenital disorder of glycosylation. This protein may also be known as HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, SLC66A5, and CDGIF.
Some mannose-P-dolichol utilization defect 1 ELISA kits can detect targets at levels as low as 0.156 ng/mL and as high as 10 ng/mL. Use the search filters to narrow your search and click on the ELISA kits below for more detailed information, such as reactivity and assay sensitivity.