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C250

Recombinant Human PMM2/Phosphomannomutase 2

10ug

1200

1080

现货

国产

C250

Recombinant Human PMM2/Phosphomannomutase 2

50ug

3520

3168

现货

国产

C250

Recombinant Human PMM2/Phosphomannomutase 2

500ug

12320

11088

现货

国产

C250

Recombinant Human PMM2/Phosphomannomutase 2

1mg

17600

15840

现货

国产

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  • Catalog# C250
    Source E.coli
    Description Recombinant Human Phosphomannomutase 2/PMM2 is produced by our E. coli expression system. The target protein is expressed with sequence (Met1-Ser246) of Human PMM2 fused with a His tag at the C-terminus.
    Names Phosphomannomutase 2, PMM 2, PMM2
    Accession # O15305
    Formulation Supplied as a 0.2 μm filtered solution of 20mM Tris-HCl, 150mM NaCl, pH 8.0
    Shipping The product is shipped on dry ice/ice packs.
    Storage Store at < -20°C, stable for 6 months after receipt.
    Please minimize freeze-thaw cycles.
    Purity Greater than 95% as determined by reducing SDS-PAGE.
    Endotoxin Less than 0.1 ng/μg (1 IEU/μg).
    Amino Acid Sequence
    MAAPGPALCLFDVDGTLTAPRQKITKEMDDFLQKLRQKIKIGVVGGSDFEKVQEQLGNDVVEKYD YVFPENGLVAYKDGKLLCRQNIQSHLGEALIQDLINYCLSYIAKIKLPKKRGTFIEFRNGMLNVS PIGRSCSQEERIEFYELDKKENIRQKFVADLRKEFAGKGLTFSIGGQISFDVFPDGWDKRYCLRH VENDGYKTIYFFGDKTMPGGNDHEIFTDPRTMGYSVTAPEDTRRICELLFSLEHHHHHH
    Background Phosphomannomutase 2 (PMM2) is an enzyme that is a member of the highly variable methyltransferase superfamily. PMM2 is a cytoplasmic protein and catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate.In addition, PMM2 involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose that required for a number of critical mannosyl transfer reactions. Defects in PMM2 can results in congenital disorder of glycosylation type 1A (CDG1A). Congenital disorders of glycosylation are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation.