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Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. Additionally we are shipping Mitochondrially Encoded ATP Synthase 6 Antibodies (4) and and many more products for this protein.
Mice were created that allotopically express either a mutant (A6M) or wildtype (A6W) mt-Atp6 transgene.
ATP6 genetic polymorphisms associated with breast cancer in Mizoram mongloid population.
analysis of mitochondrial deletion and double mutations in the MT-ATP6 gene in Tunisian patients
Two synonymous substitutions (mt.8614T>C and mt.8994G>A) in the mt-ATP6 gene may be associated with childhood obesity; study provides first data about mitochondrial genome variations in a Turkish obese population and also the first in obese children
This study suggests that, in part, polymorphisms in the MT-ATP6 and MT-CYB (show MT-CYB ELISA Kits) genes may contribute to the unexpected fertilization failure.
T8821G mutation of the ATPase6 is associated with Leber's hereditary optic neuropathy.
Screening of the MT-ATP6 gene in a large collection of patients suspected of suffering different mitochondrial DNA (mtDNA) disorders. Biochemical, molecular-genetics and other analyses show three new pathologic mutations.
Five mutations able to change amino acid synthesis for the ATP synthase subunit 6 were associated with acute lymphoblastic leukemia in a Saudi Arabian cohort.
identified 8 changes in ATP6 gene in 36/50 examined breast cancer cell samples and 5 changes in ATP8 (show MT-ATP8 ELISA Kits) gene (10/50); most were homoplasmic changes of missense type; 4 changes (A8439C, G8858C, C9130G and T9119G) had not been described in the literature before
Lack of Atp6 (F0-a) alters the structure but not the content of ATP synthase.
Case Report: absence of mtDNA-encoded ATPase6 and ATPase8 (show MT-ATP8 ELISA Kits) genes in progressive external ophthalmoplegia patient clearly resulted in aberrant synthesis of ATP synthase.
Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Key component of the proton channel\; it may play a direct role in the translocation of protons across the membrane.