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

Holocytochrome C Synthase (HCCS) Peptide

HCCS Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN936361
  • Target See all HCCS products
    HCCS (Holocytochrome C Synthase (HCCS))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    PAHQERAYEY VECPIRGTAA ENKENLDPSN LMPPPNQTPA PDQPFALSTV
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of HCCS antibody,
    Alternative Names: HCCS control peptide, HCCS antibody Blocking Peptide, Anti-HCCS Blocking Peptide, holocytochrome c synthase Blocking Peptide, CCHL Blocking Peptide, DKFZp779I1858 Blocking Peptide, MCOPS7 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
    HCCS (Holocytochrome C Synthase (HCCS))
    Synonyms
    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
    Background
    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.
    Molecular Weight
    30 kDa
You are here:
Support