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Sino Biological Inc. liefert Phosphomannomutase 2 / PMM2 / CDG1 Protein (His Tag) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.
Weitere Informationen über Phosphomannomutase 2 / PMM2 / CDG1 Protein (His Tag) lesen Sie bitte:http://www.sinobiological.com/Phosphomannomutase-2-PMM2-CDG1-Protein-Antibody-a-6211.html
| Synonym | PMM2 |
| Protein Construction | A DNA sequence encoding the human PMM2 (O15305) (Met1-Ser246) was expressed with a polyhistidine tag at the N-terminus. |
| Source | Human |
| Expression Host | E.coli |
| Purity | > 95 % as determined by SDS-PAGE | SDS-PAGE:![]() PMM2 protein |
| Endotoxin | Please contact us for more information. | |
| Stability | Samples are stable for up to twelve months from date of receipt at -70℃ | |
| Predicted N terminal | His | |
| Molecular Mass | The recombinant human PMM2 consists of 261 amino acids and predicts a molecular mass of 29.9 KDa. It migrates as an approximately 28 KDa band in SDS-PAGE under reducing conditions. | |
| Formulation | Lyophilized from sterile 20mM Tris,100mM NaCl, 10% Glycerol, pH 8.0.
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| Storage | Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
| Reconstitution | A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information. |
Phosphomannomutase 2, also known as PMM2 and CDG1, belongs to the eukaryotic PMM family. Phosphomannomutase 2 catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate. Mannose 1-phosphate is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. GDP-mannose can transfer its small sugar molecule called mannose to the growing oligosaccharide chain. Once the correct number of small sugar molecules are linked together to form the oligosaccharide, it can be attached to a protein. Phosphomannomutase 2 is also required for a number of critical mannosyl transfer reactions. Mutations in PMM2 gene have been shown to cause defects in the protein glycosylation pathway manifest as carbohydrate-deficient glycoprotein syndrome type I.