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5-Methyltetrahydrofolate-Homocysteine Methyltransferase Reductase (MTRR) (N-Term) Peptid

MTRR Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN980362

Kurzübersicht für 5-Methyltetrahydrofolate-Homocysteine Methyltransferase Reductase (MTRR) (N-Term) Peptid (ABIN980362)

Target

MTRR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase Reductase (MTRR))

Spezies

Human

Quelle

  • 2
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Sequenz

    YDLKTETAPL VVVVSTTGTG DPPDTARKFV KEIQNQTLPV DFFAHLRYGL

    Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti-MTRR Antibody(ARP57657_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Aufreinigung

    Purified
  • Applikationshinweise

    Each Investigator should determine their own optimal working dilution for specific applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    MTRR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase Reductase (MTRR))

    Hintergrund

    Methionine is an essential amino acid required for protein synthesis and one-carbon metabolism. Its synthesis is catalyzed by the enzyme methionine synthase. Methionine synthase eventually becomes inactive due to the oxidation of its cob(I)alamin cofactor. The protein encoded by this gene regenerates a functional methionine synthase via reductive methylation. It is a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. Patients of the cbl-E complementation group of disorders of folate/cobalamin metabolism are defective in reductive activation of methionine synthase. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms.

    Alias Symbols: MGC129643, MSR, cblE

    Protein Interaction Partner: MMAB

    Protein Size: 725

    Molekulargewicht

    80 kDa

    Gen-ID

    4552

    NCBI Accession

    NM_024010, NP_076915

    UniProt

    Q9UBK8
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