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Mouse Monoclonal Anti-Mannose Phosphate Isomerase antibody (STJ99059)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
|PMI1 antibody|CDG1B antibody|FLJ39201 antibody|Mannose 6 phosphate isomerase antibody|Mannose-6-phosphate isomerase antibody|MANNOSEPHOSPHATE ISOMERASE antibody|MGC94106 antibody|MPI antibody|MPI_HUMAN antibody|Phosphohexomutase antibody|phosphomannose isomerase 1 antibody|Phosphomannose isomerase antibody|PMI antibody|Anti-Mannose Phosphate Isomerase antibody [EPR10234] (ab154198)
SCBT cat No: sc-393484|sc-161875|sc-393477|
Anti-Mannose Phosphate Isomerase antibody
|Catalogue No.|| |
Anti-Mannose Phosphate Isomerase antibody detects endogenous levels of Mannose Phosphate Isomerase and does not cross-react with related proteins.
Purified recombinant human Mannose Phosphate Isomerase protein fragments expressed in E.coli.
|Recommended dilution|| |
WB 1:500-2000; ELISA 1:10000-20000
|Molecular weight|| |
Anti-Mannose Phosphate Isomerase antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Anti-Mannose Phosphate Isomerase antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
PMI1 antibody, CDG1B antibody, FLJ39201 antibody, Mannose 6 phosphate isomerase antibody, Mannose-6-phosphate isomerase antibody, MANNOSEPHOSPHATE ISOMERASE antibody, MGC94106 antibody, MPI antibody, MPI_HUMAN antibody, Phosphohexomutase antibody, phosphomannose isomerase 1 antibody, Phosphomannose isomerase antibody, PMI antibody
|Database links|| |
|Protein function|| |
Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.
|Protein tissue specificity|| |
Expressed in all tissues, but more abundant in heart, brain and skeletal muscle.
|Involvement in disease|| |
Congenital disorder of glycosylation 1B (CDG1B) [MIM:602579]: A form of congenital disorder of glycosylation, a multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in 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. CDG1B is clinically characterized by protein-losing enteropathy. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the mannose-6-phosphate isomerase type 1 family.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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