Plant/Algal cell antibodies
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- Global antibodies
- Protein standards-quantitation
- Loading controls
- Compartment markers
- Developmental biology
- DNA/RNA/cell cycle
- Environmental stress
- Food proteins
- Mitochondria | Respiration
- Membrane transport system
- Nitrogen metabolism
- Plant pathogens
- Control serum | Pre-immune
- Tag antibodies
- Anti-guinea pig
- Anti mouse
- Blocking /control
Animal cell antibodies
- Carrier proteins
- Fish proteins
- Human proteins
- Anti-bovine IgG
- Anti-cat IgG
- Anti-chicken IgY
- Anti-guinea pig
- Blocking /control
- Bacterial/fungal antibodies
- Anti-guinea pig
- Detection reagents
AtpB | beta subunit of ATP synthase (100 ĩl)
AS05 085 | clonality: polyclonal | host: rabbit | reactivity: [global antibody] for plant, green alga, animal and bacterial F-type ATP synthases
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1:100 (IF), 1: 2000 - 1: 5 000 with standard ECL (WB), 1: 5000 (BN-PAGE)
|expected | apparent MW||
53.9 kDa (Arabidopsis thaliana), 51.7 kDa (Synechocystis PCC 6803), 53.7 kDa (Spinacia oleracea)
Arabidopsis thaliana, Bacillus cereus, Chlamydomonas reinhardtii, Hordeum vulgare, Glycine max, Lycopersicum esulentum, Oryza sp. (roots, leafs, pollen), Nicotiana bentamiana, Nicotiana tabacum, Plasmodium berghei, Populus sp., Spinacia oleracea, Zea mays
Animal tissues from: cow, chicken, pig, rat, salmon, seal, Locusta migratoria
dicots, including Vitis vinifera, and monocots:Triticum aestivum, algae, cyanobacteria, marine diatoms, Acinetobacter baumannii, Clostridium sp., bacteria including E.coli K-12, Trichodesmium erythraeum, Salmonella typhimurium, Yrsinia sp.,
|not reactive in||
archeal V-type ATP synthase
Blue Native gel electrophoresis (BN-PAGE) has been performed on samples solubilized with digitonin (4:1) and loaded at 100 µg/well. Gel thickness was 2 mm with 4.5-16 % gradient.
Antibody is recognizing mitochondrial form of AtpB Subota el. al (2011).
|selected references||Rurek et al. (2015). Biogenesis of mitochondria in cauliflower (Brassica oleracea var. botrytis) curds subjected to temperature stress and recovery involves regulation of the complexome, respiratory chain activity, organellar translation and ultrastructure. Biochim Biophys Acta. 2015 Jan 21. pii: S0005-2728(15)00016-X. doi: 10.1016/j.bbabio.2015.01.005.
Eom et al. (2014). Bacillus subtilis HJ18-4 from Traditional Fermented Soybean Food Inhibits Bacillus cereus Growth and Toxin-Related Genes. J Food Sci. 2014 Nov;79(11):M2279-87. doi: 10.1111/1750-3841.12569. Epub 2014 Oct 30.
Lintala et al. (2013). Arabidopsis tic62 trol mutant lacking thylakoid bound ferredoxin-NADP+ oxidoreductase shows distinct metabolic phenotype. Mol Plant Sep 16.
Teng et al. (2013). Mitochondrial Genes of Dinoflagellates Are Transcribed by a Nuclear-Encoded Single-Subunit RNA Polymerase. PLOS ONE, June 2013. (immuofluorescence)
Rasala et al. (2013). Expanding the spectral palette of fluorescent proteins for the green microalga Chlamydomonas reinhardtii. Plant J. March 23.
Heinnickel et al. (2013). Novel thylakoid membrane greencut protein cpld38 impacts accumulation of the cytochrome b6f complex and associated regulatory processes. J. Biol. Chem. Jan 9.
2 µg of total protein extracted with PEB (AS08 300) from leaf tissue of (1) Arabidopsis thaliana, (2) Spinacia oleracea, (3) Lycopersicon esculentum, (4) Glycine max, (5) Populus sp., (6) Zea mays and (7) Hordeum vulgare were separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 1h to nitrocellulose. In parallel a dilution row (a-g: 10 - 5 - 2.5 - 1.25 - 0.63 - 0.32 - 0.16 µg protein/lane) from sample 1 (Arabidopsis) was processed. Filters were blocked 1h with 2% low-fat milk powder in TBS-T (0.1% TWEEN 20) and probed with anti-AtpB (AS08 085, 1:5000, 1h) and secondary anti-rabbit (1:10000, 1 h) antibody (HRP conjugated, recommended secondary antibody AS09 602) in TBS-T containing 2% low fat milk powder. Antibody incubations were followed by washings in TBS-T (15, +5, +5, +5 min). All steps were performed at RT with agitation. Signal was detected with standard ECL (Invitrogen) using a Fuji LAS-3000 CCD (300s, standard sensitivity).
application example 2
2 µg of total protein from (1) cow muscle, (2) chicken muscle, (3) pig muscle, (4) rat liver, (5) salmon muscle, (6) seal muscle, (8) Arabidopsis thaliana, (9) Zea mays extracted with Protein Extration Buffer, PEB (AS08 300) and separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 1h to PVDF. Blots were blocked immediately following transfer in 2% ECL Advance blocking reagent (GE Healthcare) in 20 mM Tris, 137 mM sodium chloride pH 7.6 with 0.1% (v/v) Tween-20 (TBS-T) for 1h at room temperature with agitation. Blots were incubated in the primary antibody at a dilution of 1: 50 000 for 1h at room temperature with agitation. The antibody solution was decanted and the blot was rinsed briefly twice, then washed once for 15 min and 3 times for 5 min in TBS-T at room temperature with agitation. Blots were incubated in secondary antibody (Agrisera anti-rabbit IgG horse radish peroxidase conjugated, AS09 602) diluted to 1:50 000 in 2% ECL Advance blocking solution for 1h at room temperature with agitation. The blots were washed as above and developed for 5 min with ECL Advance detection reagent according to the manufacturers instructions. Images of the blots were obtained using a CCD imager (FluorSMax, Bio-Rad) and Quantity One software (Bio-Rad). Exposure time was 30 seconds.
M - molecular weight marker
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AS09 602 | Goat anti-rabbit IgG (H&L), HRP conjugated
AS09 607 | Goat anti-rabbit IgG (H&L), ALP conjugated
AS10 1489 | Rabbit anti-Chicken IgY (H&L), HRP conjugated
AS09 606 | Goat anti-chicken IgY (H&L), ALP conjugated
For a complete list of Agrisera secondary antibodies
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AgriseraECL Bright for Western Blot detection is a high quality substrate for detection of horseradish peroxidase enzyme activity at a femtogram level. Its a ready to use 2 component system with low background and superior signal to nouse ratios.
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TMB based, one component, especially formulated with extreme sensitivity, HRP substrate for microwell application.