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Phosphomannomutase catalyzes the conversion between D-mannose 6-phosphate and D-mannose 1-phosphate which is a substrate for GDP-mannose synthesis. Zusätzlich bieten wir Ihnen Phosphomannomutase 1 Antikörper (17) und viele weitere Produktgruppen zu diesem Protein an.
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human alpha-phosphomannomutase 1 crystallographic structure reveals the structural basis of congenital disorder of glycosylation type 1a
The genes GUS (zeige GUSB Proteine) and PMM1 are recommended for normalization purposes in gene expression studies of liver tissue from patients with chronic hepatitis.
PMM1 is responsible for the degradation of Glc-1,6-P(2) in brain
Pmm1 activity in jejunum increased during the early stages of life, and it decreased at 1 month old, as does the amount of mannose incorporated into glycoproteins, whereas in the ileum, they were not affected by age.
Pmm1 immunoreactivity seen in prenatal brain until postnatal and adult stage and restricted in neuronal cell bodies.
The normal phenotype of Pmm1-deficient mice suggests that Pmm1 is not essential for normal mouse development.
Phosphomannomutase catalyzes the conversion between D-mannose 6-phosphate and D-mannose 1-phosphate which is a substrate for GDP-mannose synthesis. GDP-mannose is used for synthesis of dolichol-phosphate-mannose, which is essential for N-linked glycosylation and thus the secretion of several glycoproteins as well as for the synthesis of glycosyl-phosphatidyl-inositol (GPI) anchored proteins.
, PMM 1
, brain glucose-1,6-bisphosphatase
, Secp53 homolog