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Coagulation Factor VIII (F8) (C-Term) Peptide

F8 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN976555
  • Target See all Factor VIII (F8) products
    Factor VIII (F8) (Coagulation Factor VIII (F8))
    Protein Region
    C-Term
    Origin
    Human
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Sequence
    GSKGEKGERG RAGELGEAGP SGEPGVPGDA GMPGERGEAG HRGSAGALGP
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-F8 Antibody. 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
  • Application Notes
    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.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    Factor VIII (F8) (Coagulation Factor VIII (F8))
    Synonyms
    fb61d02 Peptide, wu:fb61d02 Peptide, Cf-8 Peptide, Cf8 Peptide, FVIII Peptide, AHF Peptide, DXS1253E Peptide, F8B Peptide, F8C Peptide, HEMA Peptide, coagulation factor VIIi Peptide, coagulation factor VIII Peptide, coagulation factor VIII, procoagulant component Peptide, f7i Peptide, F8 Peptide
    Background
    This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. Mutations in this gene are associated with multiple epiphyseal dysplasia type 3.

    Alias Symbols: AHF, DXS1253E, F8B, F8C, FVIII, HEMA

    Protein Interaction Partner: COL2A1,MAG,EGFR

    Protein Size: 684
    Molecular Weight
    63 kDa
    Gene ID
    2157
    NCBI Accession
    NM_000132, NP_000123
    UniProt
    P00451
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