AtpB | Beta subunit of ATP synthase, mitochondrial
AS16 3976 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Arabidopsis thaliana, Brassica oleracea var. botrytis cv. ’Diadom’, [compartment marker] of mitochondrial inner membrane
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KLH-conjugated synthetic peptide derived from available plant, algal mitochondrial sequences of beta subunits of F-type ATP synthases, including Arabidopsis thaliana ATP synthase subunit beta-1 UniProt:P83483, TAIR:AT5G08670
ATP synthases subunit beta-2 UniProt:P83484, TAIR: AT5G08690, ATPase subunit beta-3, UniProt: Q9C5A9, TAIR:AT5G08680, which belong to mitochondrial respiratory chain complex I.
59.6 | 55 kDa
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10 and 20 µg of mitochondrial proteins from cauliflower (Brassica oleracea var. botrytis cv. ’Diadom’) curds (inflorescences) isolated as described by Rurek et al., 2015 (doi: 10.1016/j.bbabio.2015.01.005) were denatured with standard sample buffer (final concentrations in the sample: 2% SDS, 10% glycerol, 50 mM Tris-HCl pH 6.8, 0.1% bromophenol blue, 1% b-mercaptoethanol) at 80oC for 10 min. Proteins were separated on 12% SDS-PAGE and blotted 1h to Immobilon-P (Millipore) using standard Towbin buffer (25 mM Tris, 192 mM glycine, pH 8.3, 20% methanol) supplemented with SDS (0.1%) and semi-dry transfer apparatus (TE77 PWR, Hoefer). Blots were CBB R250 briefly stained (CBB was dissolved in 50% methanol, 7% acetic acid), destained (with this solution without CBB) and wet-scanned (Laser Jet Pro 400 color MFP scanner, Hewlett-Packard). Blots were blocked with 5% skimmed milk (dissolved in PBS-T containing 0.1% Tween 20) in 1h, RT with agitation. Blots were incubated in the primary antibody at a dilution of 1: 1000 for overnight (15 h) at +4ºC with agitation in PBS-T. The antibody solution was decanted and the blot was rinsed briefly, then washed 3 times for 10 min in copious amounts of PBS-T at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Agrisera; product # AS09 602) diluted to 1:30 000 in 2% milk/ PBS-T for 1h at RT with agitation. The blot was washed as above and developed for 1 min with chemiluminescent detection reagent. Exposure time was: 10, 20, 30 seconds and 1 minute and is indicated on the figure above. MW marker: PageRuler Plus (product #26619) Thermo Scientific (on Western images as dots at the left side on the panels). In red- lot 15D 3650, in blue- lot 16D 2201.
Courtesy of Dr. Michał Rurek, Department of Molecular & Cellular Biology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poland
This product can be sold containing ProClin if requested.
ATP synthase is the universal enzyme that synthesizes ATP from ADP and phosphate using the energy stored in a transmembrane ion gradient. This enzyme is localised in mitochondrial inner membrane.