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Holocytochrome C Synthase (HCCS) (N-Term) Peptide

HCCS Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN977878
  • Antigène Tous les produits HCCS
    HCCS (Holocytochrome C Synthase (HCCS))
    Protein Region
    N-Term
    Origine
    Humain
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    PAHQERAYEY VECPIRGTAA ENKENLDPSN LMPPPNQTPA PDQPFALSTV
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-HCCS 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
  • 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
    HCCS (Holocytochrome C Synthase (HCCS))
    Synonymes
    hccsb Peptide, id:ibd1278 Peptide, wu:fb18h01 Peptide, wu:fc64e12 Peptide, wu:fi43e01 Peptide, cchl Peptide, mcops7 Peptide, DDBDRAFT_0217711 Peptide, DDBDRAFT_0266707 Peptide, DDB_0217711 Peptide, DDB_0266707 Peptide, CCHL Peptide, MCOPS7 Peptide, RGD1563855 Peptide, holocytochrome c synthase b Peptide, holocytochrome c synthase Peptide, cytochrome c heme-lyase Peptide, cytochrome c-type heme lyase Peptide, holocytochrome c synthetase Peptide, hccsb Peptide, hccs Peptide, cchl Peptide, HCCS Peptide, Hccs Peptide, LOC100356413 Peptide
    Sujet
    The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.

    Alias Symbols: CCHL, DKFZp779I1858, MCOPS7

    Protein Size: 268
    Poids moléculaire
    30 kDa
    ID gène
    3052
    NCBI Accession
    NM_005333, NP_005324
    UniProt
    P53701
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