Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) Peptide

MTR Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN938943
  • Target See all MTR products
    MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    GSEQLDVADL RRLRYKGIRP APGYPSQPDH TEKLTMWRLA DIEQSTGIRL
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of MTR antibody,
    Alternative Names: MTR control peptide, MTR antibody Blocking Peptide, Anti-MTR Blocking Peptide, 5-Methyltetrahydrofolate-Homocysteine Methyltransferase Blocking Peptide, FLJ45386 Blocking Peptide
    Purification
    The antibody is affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen.
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • Target
    MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
    Synonyms
    HMAG Peptide, MS Peptide, cblG Peptide, AI894170 Peptide, D830038K18Rik Peptide, methioninesynthase Peptide, 5-methyltetrahydrofolate-homocysteine methyltransferase Peptide, MTR Peptide, Mtr Peptide
    Background
    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.
    Molecular Weight
    140 kDa
You are here:
Support