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Thymidylate Synthetase (TYMS) Peptide

TYMS Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN939139
  • Target See all TYMS products
    TYMS (Thymidylate Synthetase (TYMS))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    HIEPLKIQLQ REPRPFPKLR ILRKVEKIDD FKAEDFQIEG YNPHPTIKME
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of TYMS antibody,
    Alternative Names: TYMS control peptide, TYMS antibody Blocking Peptide, Anti-TYMS Blocking Peptide, Thymidylate Synthetase Blocking Peptide, HsT422 Blocking Peptide, MGC88736 Blocking Peptide, TMS Blocking Peptide, TS Blocking Peptide, TSase Blocking Peptide
  • 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
    TYMS (Thymidylate Synthetase (TYMS))
    Synonyms
    FN1 Peptide, ECK2823 Peptide, JW2795 Peptide, ts Peptide, Ts Peptide, HST422 Peptide, TMS Peptide, TS Peptide, thymidylate synthetase Peptide, contains intron in T4 phage Peptide, ThyE Peptide, thymidylate synthase Peptide, thymidylate synthetase L homeolog Peptide, TYMS Peptide, thyA Peptide, td Peptide, thyE Peptide, DDA3937_RS04960 Peptide, tyms.L Peptide, XBJ1_RS15770 Peptide, EAMY_RS20680 Peptide, Tyms Peptide
    Target Type
    Viral Protein
    Background
    TYMS catalyzes the methylation of deoxyuridylate to deoxythymidylate using 5,10-methylenetetrahydrofolate (methylene-THF) as a cofactor. This function maintains the dTMP (thymidine-5-prime monophosphate) pool critical for DNA replication and repair. The enzyme has been of interest as a target for cancer chemotherapeutic agents. It is considered to be the primary site of action for 5-fluorouracil, 5-fluoro-2-prime-deoxyuridine, and some folate analogs.
    Molecular Weight
    36 kDa
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