HCCS (NM_001122608) Human Recombinant Protein
Product Specifications
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. [provided by RefSeq, Jan 2010]
Overview
Recombinant protein of human holocytochrome c synthase (cytochrome c heme-lyase) (HCCS)
Synonyms
CCHL; LSDMCA1; MCOPS7; MLS
Gene ID
3052
UniProt
P53701, A0A024RBY9
Accession Number mRNA
NM_001122608
Chromosomal Location
Xp22.2
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Porphyrin and chlorophyll metabolism
Field of Research
Porphyrin and chlorophyll metabolism
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
30.4 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
HCCS
Species
Human
Protein ID
NP_001116080
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/3052
Uniprot URL
https://www.uniprot.org/uniprot/P53701
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001122608
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001116080
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