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product information
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| background |
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Catalase is an enzyme found in most living organisms which is catalazying decomposition of hydrogen peroxide to water and oxygen. In plant cells catalase is found in peroxisomes. This enzyme is involved in photorespiration and symbiotic nitrogen fixation. |
| immunogen |
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purified native catalase from Ricinus communis |
| antibody format |
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rabbit |
polyclonal, |
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ammonium sulfate purified IgG, |
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| quantity |
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| storage |
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store at -20°C; make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes. |
| tested applications |
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ELISA (ELISA), western blot (WB) |
| related products |
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AS08 374 | anti-KatG | catalase peroxidase (HPI), cyanobacterial |
| additional information |
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0.1 % sodium azide is added as preservative. For antibody re-suspending information check the tube lable. |
application information
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| recommended dilution |
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1: 8000 (ELISA), 1: 2000 with standard ECL (WB) |
| expected | apparent MW |
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57 | 55 kDa |
| confirmed reactivity |
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Ricinus communis
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| predicted reactivity |
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dicots including: Arabidopsis thaliana,Gossypium mexicanum, Vitis vinifera, monocots including: Hordeum vulgare, Oryza sativa, trees: Populus jackii
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| not reactive in |
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no confirmed exceptions from predicted reactivity known in the moment |
| additional information |
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Protein or membrane sample should be treated at 70°C for 10 min before loading on the gel. Diluted antibody solution can be used 2 to 3 times within one month if it contains 0.1 % sodium azide as preservative and is stored at -20ºC to -80ºC. Manufactured by Operon Biotechnologies. |
| selected references |
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Maeshima et al. (1992). Tissue-Specific Isoforms of Catalase Subunits in Castor Bean Seedlings. Plant and Cell Physiology 33:225-232. |
| application example SDS-PAGE of crude preparation of catalaze purified from Ricinus communis endosperm (1) and western blot detection of crude preparation of Ricinus communis endosperm proteins (2) . Proteins were separated on 12 % SDS-PAGE and blotted 1h to PVDF membrane (40 min. at 10 V using BioRad semidry transfer). Filters were blocked 1h with 5 % low-fat milk powder in TBS-T (0.05% Triton X.100). Membranes were washed 5 times with TBS-T, each time in a fresh polystyrene box and probed with anti-catalase antibodies (AS09 501, 1:1000, 1h) and secondary anti-rabbit (1:2000, 1 h). All steps were performed in RT with agitation. |  |
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