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The antibody against PMM2 was raised in rabbit using the Recombinant Human Phosphomannomutase 2 protein (1-246AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC, IP.
The antibody against PMM2 was raised in rabbit using the Recombinant Human Phosphomannomutase 2 protein (1-246AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC, IP.
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Immunohistochemistry of paraffin-embedded human thyroid tissue using PMM2 Antibody at dilution of 1:1002
| Cat.No | ADC-16567A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | PMM2 |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IHC, WB, IP | Storage | Upon receipt |
| Immunogen Description | Recombinant Human Phosphomannomutase 2 protein (1-246AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | O15305 |
Uniprot Id
O15305
Target Species
Human
Target Name
PMM2
Target Full Name
Phosphomannomutase 2
Target Function
Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.
Target Involvement
Congenital disorder of glycosylation 1A (CDG1A)
Target Subcellular Location
Cytoplasm.
Target Protein Families
Eukaryotic PMM family
Target Research Area
Signal Transduction
Target Synonyms
AI585868; BOS_22465; C86848; CDG 1; CDG1; CDG1a; CDGS; MGC127449; Phosphomannomutase 2; PMM 2; Pmm2; PMM2_HUMAN
Target Background
The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I.
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