Mouse Monoclonal Anti-Mannose Phosphate Isomerase antibody (STJ99059)


Reactivity: Human, Rat
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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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

Image descriptions:

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Alternative names:

Check alternative names for the antibody


|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.



Human, Rat


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.











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.


1 mg/ml


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

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

Cytoplasm .


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St John’s Laboratory Ltd.

Product type

Primary antibody


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