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PTPMT1 Protein (His tag)

PTPMT1 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 94 % as determined by reducing SDS-PAGE. Active
N° du produit ABIN7317331
  • Antigène Voir toutes PTPMT1 Protéines
    PTPMT1 (Protein Tyrosine Phosphatase, Mitochondrial 1 (PTPMT1))
    Type de proteíne
    Recombinant
    Activité biologique
    Active
    Origine
    • 4
    • 1
    • 1
    Humain
    Source
    • 4
    • 1
    • 1
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette PTPMT1 protéine est marqué à la His tag.
    Fonction
    Recombinant Human PTPMT1 Protein (His Tag)(Active)
    Séquence
    Lys 28-Thr 201
    Attributs du produit
    A DNA sequence encoding the human PTPMT1 isoform 1 (Q8WUK0-1) (Lys 28-Thr 201) was expressed, with a polyhistidine tag at the N-terminus.
    Pureté
    > 94 % as determined by reducing SDS-PAGE.
    Biological Activity Comment
    Measured by its ability to cleave pNPP.The specific activity is >200 pmoles/min/μg.
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    Discover our top product PTPMT1 Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Please refer to the printed manual for detailed information.
    Buffer
    Lyophilized from sterile PBS, 10 % glycerol, 1 mM DTT, pH 7.5
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Antigène
    PTPMT1 (Protein Tyrosine Phosphatase, Mitochondrial 1 (PTPMT1))
    Autre désignation
    PTPMT1 (PTPMT1 Produits)
    Synonymes
    im:7137979 Protein, zgc:158719 Protein, DUSP23 Protein, MOSP Protein, PLIP Protein, 1110001D10Rik Protein, 2810004N20Rik Protein, Plip Protein, protein tyrosine phosphatase, mitochondrial 1 Protein, PTPMT1 Protein, ptpmt1 Protein, Ptpmt1 Protein
    Sujet

    Background: PTPMT1 (PTP localized to the Mitochondrion 1) is a member of the protein tyrosine phosphatase superfamily that is localized exclusively to the mitochondrion. It has been recently reported that PTPMT1 dephosphorylates phosphatidylglycerol phosphate, an essential intermediate of cardiolipin biosynthesis. PTPMT1 deficiency in mouse embryonic fibroblasts compromises mitochondrial respiration and results in abnormal mitochondrial morphology. Lipid analysis of PTPMT1-deficient fibroblasts reveals an accumulation of PGP along with a concomitant decrease in phosphatidylglycerol. Modulation of mitochondrial ATP synthesis by PTPMT1 suggests a novel approach for the treatment of pancreatic cancers, which represent some of the deadliest forms of human tumors. The gluttony of cancer cells for energy is well established, and with the development of a modulator of expression, one may hope that we could also achieve the synthetic induction of PTPMT1 expression. It would then be expected that this effect would attenuate, if not abolish, the growth of pancreas-derived tumor cells and support the establishment of a novel regimen for pancreatic cancers. 

    Synonym: DUSP23;FLJ46081;MOSP;PLIP;PNAS-129

    Poids moléculaire
    21.7 kDa
    Pathways
    Inositol Metabolic Process
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