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5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) Peptide

MTR Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN980359
  • Antigène Tous les produits MTR
    MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
    Origine
    Humain
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-MTR antibody (Catalog #: ARP48473_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
    MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
    Synonymes
    HMAG Peptide, MS Peptide, cblG Peptide, AI894170 Peptide, D830038K18Rik Peptide, methioninesynthase Peptide, 5-methyltetrahydrofolate-homocysteine methyltransferase Peptide, MTR Peptide, Mtr Peptide
    Sujet
    MTR is the enzyme 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. MTR encodes the enzyme 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: FLJ45386, MS, cblG

    Protein Interaction Partner: DYNLL1,TSC22D1

    Protein Size: 1265
    Poids moléculaire
    140 kDa
    ID gène
    4548
    NCBI Accession
    NM_000254, NP_000245
    UniProt
    Q99707
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