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- 详细信息
- 文献和实验
- 技术资料
- 供应商:
上海经科化学科技有限公司
- 抗体英文名:
Trans-zeatin riboside | Cytokinin ELISA quantitation kit
- 规格:
1kit
| background | this ELISA assay utilise the principle of competitive binding to measure the concentration of hormone in plant extracts. The trans-zeatin riboside specific antibodies are precoated to the surface of the reaction wells. The plant extract sample, containing an unknown amount of hormone, is mixed in the reaction well with a known amount of a tracer to react with a limited number of antibodies in the reaction wells. During incubation the hormone in the sample competes with the tracer for the antibody binding sites. Unbound hormone, tracer and plant extract are washed out of the reaction wells. Following substrate addition which reacts with a tracer bound to the antibody and produces a yellow-coloured product. The absorbance of the sample is converted to concentration of hormone by means of a standard curve which is produced by simultaneously treating standards along with the samples. |
| reaction wells | antibody coated and blocked, 5pcs for 480 assays, 60 strips with 8 wells |
| tracer | 20 – 50 µl |
| tracer diluent | 5x250 mM TBS Tris, 10 mM NaCl, 1 mM MgCl2, pH 7.5 stock + 0.02 % NaN3 |
| reaction and wash solution | 10x TBS stock+0.02 % NaN3 |
| stopping reagent | 2x 5 N KOH stock |
| substrate diluent | 10x 500 mM NaHCO3 stock, pH 9.6+0 0.02 %. 0 0.02 % NaN3 |
| substrate | 100 mg |
| standards | 600 µl of each: 15.6 pmol, 7.8 pmol, 3.9 pmol, 1.95 pmol, 975 fmol, 488fmol, 244 fmol, 122 fmol, 61 fmol, 30.5 fmol, 15.2 fmol |
| assay development time | 4-5 hours |
| sensitivity | 0.01 to 10 pmol/50 µl |
| plant extract volume | 50 µl |
名称:Trans-zeatin riboside | Cytokinin ELISA quantitation kit
货号:AS11 1784
品牌:Agrisera
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文献和实验at 4°C for 15 minutes. 9. Remove and aliquot supernatant. We recommend making several 50 μl aliquots. 10. Before running ELISA, dilute protein 1:100 and run a Bradford total protein assay or Quant-iT™ Protein Quantitation Kit assay (Cat. no. Q
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