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HCCS Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech
SDP

Rabbit Polyclonal Antibody

Manufacturer:  Proteintech Group Inc 151181AP150UL

Encompass_Preferred

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Catalog No. 50-172-9995


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Description

Description

CCHL (cytochrome c-type heme lyase), also known as HCCS (holocytochrome c-type synthase), is a 268 amino acid mitochondrial inner membrane protein that belongs to the cytochrome c-type heme lyase family. Containing two HRM (heme regulatory motif) repeats, HCCS participates in the covalent linkage of a heme group to an apoprotein of cytochrome c. The gene encoding HCCS maps to the human X chromosome. Defects to this gene cause microphthalmia syndromic type 7 (MCOPS7), also known as MIDAS syndrome or microphthalmia with linear skin defects (MLS). MCOPS7 is an X-linked male-lethal disorder that results in eye deformation, unilateral or bilateral microphthalmia, linear skin defects in affected females, and in utero lethality for males.
Specifications

Specifications

HCCS
Polyclonal
Unconjugated
HCCS
CCHL, Cytochrome c type heme lyase, HCCS, Holocytochrome c type synthase, MCOPS7
Rabbit
Antigen Affinity Chromatography
RUO
15159, 3052, 317444
-20°C
Liquid
Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot
0.69 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
P53701, P53702
Hccs
HCCS Fusion Protein Ag7189
150 μL
Primary
Human, Mouse, Rat
Antibody
IgG
SDS
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Documents

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