HCCS Polyclonal Antibody

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.

Research Area: Cancer, Cardiovascular, Metabolism, Signal Transduction

Synonyms:
CCHL, CCHL, cytochrome c heme-lyase, Cytochrome c-type heme lyase, DKFZp779I1858, EC 4.4.1.17, Hccs, Holocytochrome c synthase (cytochrome c heme lyase), Holocytochrome c synthase, Holocytochrome c type synthase, Holocytochrome c-type synthase, MCOPS7, OTTHUMP00000022903, OTTHUMP00000022904, OTTHUMP00000022905, OTTMUSP00000021173, OTTMUSP00000021174, RGD1563855, RP23-37L2.1

Immunogen: Fusion protein of human HCCS

Swissprot: P53701
Gene Accession: BC001691

Calculated MW: 31 kDa
Observed MW: Refer to figures

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 1.98 mg/mL
Dilution: WB 1:5000-1:10000, IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.