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Mannose-P-dolichol utilization defect 1 protein

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Required for normal utilization of mannose-dolichol phosphate (Dol-P-Man) in the synthesis of N-linked and O-linked oligosaccharides and GPI anchors.

Below are the list of possible Mannose-P-dolichol utilization defect 1 protein 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.
 

Mannose-P-dolichol utilization defect 1 protein

 Mannose-P-dolichol utilization defect 1 protein ELISA Kit
 Mannose-P-dolichol utilization defect 1 protein Recombinant
 Mannose-P-dolichol utilization defect 1 protein Antibody
Also known as Mannose-P-dolichol utilization defect 1 protein (Suppressor of Lec15 and Lec35 glycosylation mutation homolog) (SL15).
MPDU1: Required for normal utilization of mannose-dolichol phosphate (Dol-P-Man) in the synthesis of N-linked and O-linked oligosaccharides and GPI anchors. Defects in MPDU1 are the cause of congenital disorder of glycosylation type 1F (CDG1F). CDGs are a family o
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f severe inherited diseases caused by a defect in protein N- glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. Belongs to the MPDU1 (TC 2.A.43.3) family.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Cellular Component: endoplasmic reticulum; membrane; mitochondrion

Biological Process: dolichol-linked oligosaccharide biosynthetic process; oligosaccharide biosynthetic process
 Mpdu1 ELISA Kit
 Mpdu1 Recombinant
 Mpdu1 Antibody
 Supl15h ELISA Kit
 Supl15h Recombinant
 Supl15h Antibody
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Mannose-P-dolichol utilization defect 1 protein homolog

 Mannose-P-dolichol utilization defect 1 protein homolog ELISA Kit
 Mannose-P-dolichol utilization defect 1 protein homolog Recombinant
 Mannose-P-dolichol utilization defect 1 protein homolog Antibody
 F38E1.9 ELISA Kit
 F38E1.9 Recombinant
 F38E1.9 Antibody
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Mannose-P-dolichol utilization defect 1 protein homolog 1

 Mannose-P-dolichol utilization defect 1 protein homolog 1 ELISA Kit
 Mannose-P-dolichol utilization defect 1 protein homolog 1 Recombinant
 Mannose-P-dolichol utilization defect 1 protein homolog 1 Antibody
 At5g59470 ELISA Kit
 At5g59470 Recombinant
 At5g59470 Antibody
 F2O15.15 ELISA Kit
 F2O15.15 Recombinant
 F2O15.15 Antibody
 F2O15_130 ELISA Kit
 F2O15_130 Recombinant
 F2O15_130 Antibody
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Mannose-P-dolichol utilization defect 1 protein homolog 2

 Mannose-P-dolichol utilization defect 1 protein homolog 2 ELISA Kit
 Mannose-P-dolichol utilization defect 1 protein homolog 2 Recombinant
 Mannose-P-dolichol utilization defect 1 protein homolog 2 Antibody
Required for normal utilization of mannose-dolichol phosphate (Dol-P-Man) in the synthesis of N-linked and O-linked oligosaccharides and GPI anchors.
 At4g07390 ELISA Kit
 At4g07390 Recombinant
 At4g07390 Antibody
 F28D6.6 ELISA Kit
 F28D6.6 Recombinant
 F28D6.6 Antibody
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