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Cytochrome b Polyclonal Antibody

CAT: 0965-JOT-AP00497-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0965-JOT-AP00497-01Size:20 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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 mitochondrial myopathy (MM). In mitochondrial myopathy| exercise intolerance is the predominant symptom. Additional features include lactic acidosis| muscle weakness and/or myoglobinuria. Defects in MTCYB are also found in cases of exercise intolerance accompanied by deafness| mental retardation| retinitis pigmentosa| cataract| growth retardation| epilepsy (multisystem disorder).|disease:Defects in MT-CYB are the cause of cardiomyopathy infantile histiocytoid (CMIH)
CAS Number
9007-83-4
Synonyms
Cytochrome b; Cytochrome b; Complex III subunit 3; Complex III subunit III; Cytochrome b-c1 complex subunit 3; Ubiquinol-cytochrome-c reductase complex cytochrome b subunit
Host
Rabbit
Reactivity
Human, Mouse
Immunogen
Synthesized peptide derived from human Cytochrome b. at AA range: 331-380
Clonality
Polyclonal
Applications
WB, ELISA
Stability
-20°C for 1 year
Concentration
1 mg/ml
Antibody Type
Primary antibody
Isotype
IgG

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