A15512
Size
  • 50ul
  • 100ul
Price
  • $129
  • $229
Qty
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Product description

holocytochrome c synthase(HCCS) Homo sapiens 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 transcr

Source
Rabbit
Applications
WB,IHC,IF,ELISA
Reactivity
Human,Mouse,Monkey
Dilution
WB: 1/500 - 1/2000. IHC: 1/100 - 1/300. IF: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.
Storage
-20°C/1 year
Specificity
HCCS Polyclonal Antibody detects endogenous levels of HCCS protein.
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
The antiserum was produced against synthesized peptide derived from human Cytochrome c-type Heme Lyase. AA range:81-130
Uniprot No
P53701
Alternative names
HCCS; CCHL; Cytochrome c-type heme lyase; CCHL; Holocytochrome c-type synthase
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
Background
holocytochrome c synthase(HCCS) Homo sapiens 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 transcr
Other
Gene_name: HCCS ; Protein_name: Cytochrome c-type heme lyase; Expression: Brain,Liver,Ovary,
Mol.Wt (Da)
31 kD
Concentration
1 mg/ml

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