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Phosphomannomutase

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Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.

Below are the list of possible Phosphomannomutase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Phosphomannomutase

 Phosphomannomutase ELISA Kit
 Phosphomannomutase Recombinant
 Phosphomannomutase Antibody
Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.
 PMM ELISA Kit
 PMM Recombinant
 PMM Antibody
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Phosphomannomutase 1

 Phosphomannomutase 1 ELISA Kit
 Phosphomannomutase 1 Recombinant
 Phosphomannomutase 1 Antibody
Also known as Phosphomannomutase 1 (PMM 1).
Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.
 pmmA ELISA Kit
 pmmA Recombinant
 pmmA Antibody
 DDB_G0279289 ELISA Kit
 DDB_G0279289 Recombinant
 DDB_G0279289 Antibody
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Phosphomannomutase 2

 Phosphomannomutase 2 ELISA Kit
 Phosphomannomutase 2 Recombinant
 Phosphomannomutase 2 Antibody
Also known as Phosphomannomutase 2 (PMM 2).
PMM2: Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions. Defects in PMM2 are the cause of congenital disorder of glycosylation type 1A (CDG1A); also known as carbohydrate-deficient glycoprotein syndrome type Ia (CDGS1A) or Jaeken syndrome. Congenital disorders of g
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lycosylation are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. They are characterized by under-glycosylated serum glycoproteins. CDG1A is an autosomal recessive disorder characterized by a severe encephalopathy with axial hypotonia, abnormal eye movement, and pronounced psychomotor retardation, as well as peripheral neuropathy, cerebellar hypoplasia, and retinitis pigmentosa. Patients show a peculiar distribution of subcutaneous fat, nipple retraction, and hypogonadism. Belongs to the eukaryotic PMM family.

Protein type: Carbohydrate Metabolism - amino sugar and nucleotide sugar; Carbohydrate Metabolism - fructose and mannose; EC 5.4.2.8; Isomerase

Cellular Component: cell soma; cytoplasm; cytosol

Molecular Function: phosphomannomutase activity

Biological Process: GDP-mannose biosynthetic process; mannose metabolic process; protein amino acid N-linked glycosylation; protein targeting to ER
 Pmm2 ELISA Kit
 Pmm2 Recombinant
 Pmm2 Antibody
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