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|Tested species reactivity||Bovine, C. elegans, Fruit fly, Human, Mollusc, Mouse, Rat|
|Published species reactivity||Rat, Human, Not Applicable|
|Host / Isotype||Mouse / IgG2b|
|Immunogen||Bovine Complex V|
|Storage buffer||HEPES buffered saline|
|Contains||0.02% sodium azide|
|Storage Conditions||4° C, do not freeze|
|Tested Applications||Dilution *|
|Immunocytochemistry (ICC)||1-2 ug/ml|
|Immunofluorescence (IF)||Assay Dependent|
|Western Blot (WB)||1.0 ug/ml|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
ATP synthase is extremely conserved through evolution and can be found in plants, fungi, bacteria, and animals. The ATP synthase enzyme is a transmembrane protein responsible for driving the reversible reaction from ADP+ phosphate to ATP. This reaction is accomplished by a flux of protons across the membrane as a result of electron transfer. The ATP synthase protein has two main sections; the F1 ATP-ase (soluble) and the F0 ATP-ase (membrane embedded). The F1 section consists of the alpha, beta, gamma, delta, and epsilon subunits. While the F0 consists of a, b, and c subunits.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
|Not Applicable||Not Cited||
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy.
43-9800 was used in western blot to study muscular dystrophy and the downstream effects of plectin mutations in epidermolysis bullosa simplex
|Winter L,Türk M,Harter PN,Mittelbronn M,Kornblum C,Norwood F,Jungbluth H,Thiel CT,Schlötzer-Schrehardt U,Schröder R||Acta neuropathologica communications (4:null)||2016|
Reducing Lissencephaly-1 levels augments mitochondrial transport and has a protective effect in adult Drosophila neurons.
43-9800 was used in western blot to learn about augmentation of mitochondrial transport and protective effect in adult Drosophila neurons by reducing lissencephaly-1 levels
|Vagnoni A,Hoffmann PC,Bullock SL||Journal of cell science (129:178)||2016|
|Human||Not Cited||A chemical cross-linking method for the analysis of binding partners of heat shock protein-90 in intact cells.||Song S,Kole S,Bernier M||BioTechniques (0:1)||2012|
Independent roles of methionine sulfoxide reductase A in mitochondrial ATP synthesis and as antioxidant in retinal pigment epithelial cells.
43-9800 was used in western blot to test if and how MsrA affects retinal pigment epithelium functionality.
|Dun Y,Vargas J,Brot N,Finnemann SC||Free radical biology and medicine (65:1340)||2013|
||A chemical cross-linking method for the analysis of binding partners of heat shock protein-90 in intact cells.||Song S,Kole S,Bernier M||BioTechniques (0:1)||2012|
alpha subunit; ATP synthase; ATP synthase alpha chain; ATP synthase alpha chain, mitochondrial; ATP synthase alpha subunit; ATP synthase subunit alpha; ATP synthase subunit alpha, mitochondrial; ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform 1; ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform 1, cardiac muscle; ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform 2, non-cardiac muscle-like 2; ATP sythase (F1-ATPase) alpha subunit; ATP5A; ATP5AL2; ATPM; cardiac muscle; epididymis secretory sperm binding protein Li 123m; H+ transporting; hATP1; iso; isoform 1; mitochondrial; mitochondrial ATP synthetase, oligomycin-resistant; mitochondrial F1 complex; mitochondrial H+-ATP synthase alpha subunit; modifier of Min 2; MOM2; OMR; ORM
AI035633; AL022851; AL023067; ATP5A; ATP5A1; ATP5A2; ATP5AL2; ATPM; BOS_22238; COXPD22; D18Ertd206e; hATP1; HEL-S-123m; MC5DN4; MOM2; OMR; ORM