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MEP1A Protein (AA 22-601) (His tag)

MEP1A Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 90 % by SDS - PAGE SDS Active
N° du produit ABIN6387876
  • Antigène Voir toutes MEP1A Protéines
    MEP1A (Meprin A, alpha (PABA Peptide Hydrolase) (MEP1A))
    Type de proteíne
    Recombinant
    Activité biologique
    Active
    Attributs du protein
    AA 22-601
    Origine
    • 4
    • 4
    Humain
    Source
    • 4
    • 2
    • 2
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette MEP1A protéine est marqué à la His tag.
    Application
    SDS-PAGE (SDS)
    Séquence
    MGSSHHHHHH SSGLVPRGSH MAAYKLVLIR HGESAWNLEN RFSGWYDADL SPAGHEEAKR GGQALRDAGY EFDICFTSVQ KRAIRTLWTV LDAIDQMWLP VVRTWRLNER HYGGLTGLNK AETAAKHGEA QVKIWRRSYD VPPPPMEPDH PFYSNISKDR RYADLTEDQL PSCESLKDTI ARALPFWNEE IVPQIKEGKR VLIAAHGNSL RGIVKHLEGL SEEAIMELNL PTGIPIVYEL DKNLKPIKPM QFLGDEETVR KAMEAVAAQG KAKK
    Pureté
    > 90 % by SDS - PAGE
    Biological Activity Comment
    Specific activity is >300 units/mg, in which One unit will convert 1.0 umole of 3-phosphoglycerate to 2-phosphoglcerate per minute at pH 7.6 at 37C.
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    Discover our top product MEP1A Protéine
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    Liquid. In 20  mM Tris-HCl buffer(  pH 8.0) containing 10 % glycerol, 1  mM DTT
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles.
  • Antigène
    MEP1A (Meprin A, alpha (PABA Peptide Hydrolase) (MEP1A))
    Autre désignation
    MEP1A (MEP1A Produits)
    Synonymes
    AI098089 Protein, AW107200 Protein, Mep-1 Protein, Mep-1a Protein, Mep1 Protein, PPHA Protein, meprin A subunit alpha Protein, meprin 1 alpha Protein, Mep1a Protein, MEP1A Protein
    Sujet
    PGAM1 belongs to the phosphoglycerate mutase family. This protein is important components of glucose and 2,3-BPGA (2,3-bisphosphoglycerate) metabolism and catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). Mutations in this protein cause muscle phosphoglycerate mutase efficiency, also known as glycogen storage disease X. Recombinant human PGAM protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.
    Poids moléculaire
    30.9 kDa (274aa), confirmed by MALDI-TOF
    NCBI Accession
    NP_002620
    UniProt
    P18669
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