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Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity).. Additionally we are shipping Mitochondrially Encoded Cytochrome B Antibodies (34) and Mitochondrially Encoded Cytochrome B Proteins (3) and many more products for this protein.
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An analysis of eight structures of mitochondrial bc(1) with bound quinol oxidation (Q(o)) site inhibitors revealed that the presence of inhibitors causes a bidirectional repositioning of the cd1 helix in the cytochrome b subunit.
mt-Cytb mutations were studied in a mouse cultured cell model. Complex III assembly was impeded and caused a severe reduction in the amount of Complex I.
Mitochondrial mutation m.15804T>C in the mtCYB gene in a family with fibromyalgia is associated with NLRP3 (show NLRP3 ELISA Kits)-inflammasome activation.
These results indicate that miR (show MLXIP ELISA Kits)-151a-5p may participate in the regulation of cellular respiration and ATP production through targeting Cytb.
This study suggests that, in part, polymorphisms in the MT-ATP6 (show MT-ATP6 ELISA Kits) and MT-CYB genes may contribute to the unexpected fertilization failure.
The polymorphisms of CYTB as a very useful DNA marker were significantly different between different geographical Uyghur
Significant elevation of ERalpha (show ESR1 ELISA Kits) and MTCYB transcript levels in premenopausal leiomyomas and its association with ERalpha (show ESR1 ELISA Kits), -397 CC genotype suggests the mitochondrial-mediated role of estrogen as the promoter of leiomyoma tumorigenesis.
Data show that homoplasmic G6709A (MT-CO1) and G14804A (MT-CYB) alterations cause amino acid changes in the highly conserved residues.
mitocryptide-2 (MCT-2 (show SLC16A7 ELISA Kits)) and its human homolog hMCT-2 are cryptides that activate neutrophils
The other proband had a non-synonymous G15221A mutation in the cytochrome b gene.
In a mitochondrial myopathy patient, a novel stop-codon mutation (G15761A) was found in the mitochondrial DNA (mtDNA)-encoded cytochrome b gene, resulting in loss of the last 41 amino acids of the protein and complex III deficiency
biochemical and molecular genetic studies of a patient with both muscle and brain involvement and a severe reduction in the activities of both complexes I and III in skeletal muscle due to a novel mutation in the MTCYB gene
Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity).