Plant/Algal cell biology / Physcomitrella patens

product information

Glutamine synthetase (GLN or GS) is one of the key enzymes involved in nitrogen metabolism of plants. It catalyses the synthesis of glutamine from glutamate and ammonia in an ATP-dependent reaction. There are two general classes of glutamine synthetase in plants: GLN1, a cytosolic form and GLN2, a chloroplastic form. GLN1 is highly abundant in the vascular elements of roots nodules, flowers and fruits, functioning in the assimilation of ammonium and the biosynthesis of glutamine for nitrogen transport. GLN2 is encoded by a single gene and is highly abundant in leaf mesophyll chloroplasts. Here GLN functions in the assimilation of ammonia produced from photorespiration and the reduction of nitrate in the chloroplasts

KLH-conjugated synthetic peptide derived from a wide range of available sequences including all isoforms of Arabidopsis thaliana GLN1-1,1-2,1-3 and 1-4

store lyophilized/reconstituted at -20°C; once reconstituted 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.

western blot (WB)

AS08 296 GLN | GS2, chloroplastic form of glutamine synthetase

collection of antibodies to proteins involved in nitrogen metabolism

to be added when available

application information

1:10000 on 0.5-15 ug protein (WB)

39-40 GLN1kDa (cytoplasmic form) , 44-45 kDa GLN2 (chloroplastic form)

Arabidopsis thaliana, Spinacia oleracea, Zea mays, red alga Gracilaria gracilis

GLN1 dicots including: Brassica napus, Phaseolus. vulgaris, monocots including: Hordeum vulgare, Oryza sativa, trees: Pinus sylvestris, Populus sp. moss: Physcomitrella patens
GLN2 dicots including: Brassica napus, Glycine max, Phaseolus vulgaris, monocots including: Triticum aestivum, Oryza sativa

no confirmed exceptions from predicted reactivity known in the moment

to be added when available

to be added when available

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 (MagicMark^TM,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).