85-6170-89　Cytochrome b Polyclonal Antibody 20ul　BT-AP00497

特徴

• 背景：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)

仕様

• サイズ：20ul
• 抗原：Synthesized peptide derived from human Cytochrome b. at AA range: 331-380
• 免疫動物：Rabbit
• 交差性：Human, Mouse
• 適用：WB, ELISA
• クラス：IgG
• クロナリティ：Polyclonal
• 濃度：1 mg/ml
• 別名：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
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