A13354
Size
  • 50ul
  • 100ul
Price
  • $129
  • $229
Qty
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Product description

cofactor:Binds 2 heme groups non-covalently.,disease:Defects in MT-CYB are a rare cause of mitochondrial dysfunction underlying different myopathies. They include mitochondrial encephalomyopathy, hypertrophic cardiomyopathy (HCM), and sporadic mitochondri

Source
Rabbit
Applications
WB,ELISA
Reactivity
Human,Mouse
Dilution
WB 1:500-2000, ELISA 1:10000-20000
Storage
-20°C/1 year
Specificity
Cytochrome b Polyclonal Antibody detects endogenous levels of Cytochrome b
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
Synthesized peptide derived from human Cytochrome b. at AA range: 331-380
Uniprot No
P00156
Alternative names
Cytochrome b (Complex III subunit 3) (Complex III subunit III) (Cytochrome b-c1 complex subunit 3) (Ubiquinol-cytochrome-c reductase complex cytochrome b subunit)
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
Background
cofactor:Binds 2 heme groups non-covalently.,disease:Defects in MT-CYB are a rare cause of mitochondrial dysfunction underlying different myopathies. They include mitochondrial encephalomyopathy, hypertrophic cardiomyopathy (HCM), and sporadic mitochondri
Other
Gene_name: MT-CYB ; Protein_name: Cytochrome b; Expression: Bone fossil,Heart,Lymphoblast,Placenta,
Mol.Wt (Da)
48 kD
Concentration
1 mg/ml

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