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

MTRR Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN980362

Aperçu rapide pour 5-Methyltetrahydrofolate-Homocysteine Methyltransferase Reductase (MTRR) (N-Term) Peptide (ABIN980362)

Antigène

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

Origine

Humain

Source

  • 2
Synthetic

Application

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

    N-Term

    Séquence

    YDLKTETAPL VVVVSTTGTG DPPDTARKFV KEIQNQTLPV DFFAHLRYGL

    Attributs du produit

    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.

    Purification

    Purified
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

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

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

    Sujet

    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

    Poids moléculaire

    80 kDa

    ID gène

    4552

    NCBI Accession

    NM_024010, NP_076915

    UniProt

    Q9UBK8
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