HCCS rabbit pAb
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 transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010],
Product Specifications
Background
Product Name Alternative
HCCS; CCHL; Cytochrome c-type heme lyase; CCHL; Holocytochrome c-type synthase
UniProt
P53701
Swiss Prot
P53701
Reactivity
Human; Mouse; Monkey
Immunogen
The antiserum was produced against synthesized peptide derived from human Cytochrome c-type Heme Lyase. AA range:81-130
Target
HCCS
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Buffer
-20°C/1 year
Molecular Weight
31kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
31kD
Fragment
IgG
Subcellular Location
Mitochondrion inner membrane . Membrane ; Lipid-anchor .
Other Product Names
HCCS; CCHL; Cytochrome c-type heme lyase; CCHL; Holocytochrome c-type synthase
Gene ID (Human)
3052
Available Sizes
Frequently Asked Questions
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