Phospho-S6RP (Ser235/236) cellular kit
Highly sensitive and robust kit to detect Phospho-S6RP (Ser235/236)
This HTRF kit enables the cell-based quantitative detection of phosphorylated RSK1 Thr359.
The Phospho-RSK1 (T359) Cellular kit is designed for the robust quantification of RSK1 phosphorylation at Threonine359 directly using a streamlined mix-and-read, no-wash protocol. RSK1 plays a pivotal role in cell proliferation and differentiation. This kit can be used from basic research to high throughput drug screening. Its versatility means it is suitable for many applications, ranging from basic research to the analysis of pharmacological questions in cellular models.
The phospho-RSK1 assay measures RSK1 phosporylated at T59. Unlike Western Blot, the assay is entirely plate-based and does not require gels, electrophoresis, or transfer. The Total RSK1 assay uses 2 labeled antibodies: one with a donor fluorophore, the other with an acceptor. The first antibody was selected for its specific binding to the phosphorylated motif on the protein, the second for its ability to recognize the protein independent of its phosphorylation state. Protein phosphorylation enables an immune-complex formation involving both labeled antibodies and which brings the donor fluorophore into close proximity to the acceptor, thereby generating a FRET signal. Its intensity is directly proportional to the concentration of phosphorylated protein present in the sample, and provides a means of assessing the protein’s phosphorylation state under a no-wash assay format.
The 2 plate protocol involves culturing cells in a 96-well plate before lysis. Then lysates are transferred into a 384-well low volume detection plate before the addition of HTRF Phospho-RSK1 (T359) detection reagents. This protocol enables the cells' viability and confluence to be monitored.
Detection of Phospho-RSK1 (T359) with HTRF reagents can be performed in a single plate used for culturing, stimulation, and lysis. No washing steps are required. This HTS designed protocol enables miniaturization while maintaining robust HTRF quality.
A431 cells were plated under 100 µl in a 96-well plates (80,000 cells/well) in complete culture medium and incubated overnight at 37°C, 5% CO2. The day after, cells were treated with 50 µl of increasing concentrations of EGF for 5 min at 37°C, 5% CO2.
After medium removal, cells were then lysed with 100 µL of supplemented lysis buffer #2 for 30 minutes at RT under gentle shaking, and 16 µL of lysate were transferred into a low volume white microplate before the addition of 2 µL of the HTRF D2 detection reagent and 2 µL HTRF Eu-K detection reagent. Total RSK1 and phospho-RSK1 T359 were quantified in separate wells. The HTRF signal was recorded after ON incubation.
The Ribosomal protein S6 kinase alpha-1 (RSK1) is a downstream component of the MAP kinase and ERK signaling pathway and participates to the regulation of transcription factors, cell proliferation, survival, and differentiation with Serine/Threonine kinase.
It is phosphorylated at Thr359/Ser363 by MAPK1/ERK as an initial activation, and then autophosphorylates at Ser380 which allow PDK1 binding.
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Physiologically relevant results fo fast flowing research - Flyers
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Valuable guidelines for efficiently analyzing and interpreting results - Application Notes
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HTRF and WB compatible guidelines - Technical Notes
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Unmatched ease of use, sensitivity and specificity assays - Videos
Get the brochure about technology comparison. - Brochures
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A fun video introducing you to phosphorylation assays with HTRF - Videos
Insight into the diversity of cells & signaling pathways - Guides
64RSK1T9PEG-64RSK1T9PEH - Product Insert
Seeding and lysing recommendations for a number of cell culture vessels. - Technical Notes
Combination of AlphaLISA®, HTRF®, or AlphaLISA® SureFire® Ultra™ immunoassays with the ATPlite™ 1step cell viability assay - Application Notes
Learn how to reduce time and sample consumption - Application Notes
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