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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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