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Plant/Algal cell antibodies
- Protein standards-quantitation
- Global antibodies
- Compartment markers
- Bioenergetics
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- Food proteins
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Animal cell antibodies
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- Secondary antibodies
GLN1 GLN2 | GS1 GS2 glutamine synthetase global antibody
AS08 295 | clonality: polyclonal | host: rabbit | reactivity: [global antibody] | A. thaliana, Z. mays, S. oleracea, P.patens, red alga Gracilaria gracilis
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| application information |
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| recommended dilution | 1:10 000 withn 0.5-15 ug protein/well (WB) |
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| expected | apparent MW | 39-40 kDa (GLN1,cytoplasmic form) , 44-45 kDa (GLN2, chloroplastic form) |
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| confirmed reactivity | Arabidopsis thaliana, Spinacia oleracea, Zea mays, moss: Physcomitrella patens red alga Gracilaria gracilis |
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| predicted reactivity | GLN1 dicots including: Brassica napus, Phaseolus vulgaris, monocots including: Hordeum vulgare, Oryza sativa, trees: Pinus sylvestris, Populus sp., C
GLN1 in algae: Chlamydomonas reinhardii |
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| not reactive in | no confirmed exceptions from predicted reactivity known in the moment |
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| additional information | to be added when available |
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| selected references | Podgórska et al. (2013). Long-term ammonium nutrition of Arabidopsis increases the extrachloroplastic NAD(P)H/NAD(P)+ ratio and mitochondrial reactive oxygen species level in leaves but does not impair photosynthetic capacity. Plant Cell Environ. April 10. Brouwer et al. (2011) The Impact of Light Intensity on Shade-Induced Leaf Senescence. Plant Cell Environ. Dec. 15 (ahead of print). Lang, E.G.E., S.J. Mueller, S.N.W. Hoernstein, J. Porankiewicz-Asplund, M. Vervliet-Scheebaum, R. Reski (2010). Simultaneous isolation of pure and intact chloroplasts and mitochondria from moss as basis for sub-cellular proteomics. Plant Cell Reports, DOI: 10.1007/s00299-010-0935-4. (open source) |
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application example 0.5 µg of protein from Arabidopsis thaliana total leaf fraction (1), 15 µg of protein from Zea mays total leaf fraction (2), 5 µg of protein from Spinacia oleracea chloroplast enriched fraction (3) molecular weight markers (MagicMarkTM,Invitrogen) (M), extracted with PEB (AS08 300), were separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 1h to PVDF (Millipore). Filters were blocked 1h with 2% low-fat milk powder in TBS-T (0.1% TWEEN 20) and probed with anti-GLN1 GLN2 antibody (AS08 295, 1:10 000, 1h) and secondary anti-rabbit (1:20000, 1 h) antibody (HRP conjugated, Abcam) in TBS-T containing 2% low fat milk powder. Antibody incubations were followed by washings in TBS-T. All steps were performed at RT with agitation. Blots were developed for 5 min with ECL Advance detection reagent according the manufacturers instructions (GE Healthcare). Images of the blots were obtained using a CCD imager (FluorSMax, Bio-Rad) and Quantity One software (Bio-Rad). |
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||| For applications or usage on species others than stated as confirmed above Agrisera offers a payment-after-testing option. To learn more about this or for any questions on this product, please use the LiveChat option in the left menue bar or contact us at support@agrisera.com

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