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HTRF Human & Mouse Total STAT1 Detection Kit, 10,000 Assay Points
HTRF Human & Mouse Total STAT1 Detection Kit, 10,000 Assay Points
Shipping box for Revvity reagent kits
This HTRF kit detects cellular STAT1 and can be used as a normalization assay with our phospho-STAT1 kit for an optimal readout of JAK/STAT signaling.
| Feature | Specification |
|---|---|
| Application | Cell Signaling |
| Sample Volume | 16 µL |
This HTRF kit detects cellular STAT1 and can be used as a normalization assay with our phospho-STAT1 kit for an optimal readout of JAK/STAT signaling.
Product Variants
Unit Size: 500 Assay Points
Part #:
63ADK096PEG
List Price
USD 2,271.53
Unit Size: 10,000 Assay Points
Part #:
63ADK096PEH
List Price
USD 13,214.42
For research use only. Not for use in diagnostic procedures. All products to be used in accordance with applicable laws and regulations including without limitation, consumption and disposal requirements under European REACH regulations (EC 1907/2006).
HTRF Human & Mouse Total STAT1 Detection Kit, 10,000 Assay Points
Shipping box for Revvity reagent kits
HTRF Human & Mouse Total STAT1 Detection Kit, 10,000 Assay Points
Product information
Overview
The total STAT1 assay measures endogeneous levels of STAT1 in cell lysates. STAT1 acts as an important transcriptional activator and the assay serves as a readout for JAK inhibitors in oncology, virology, and inflammation. The assay can be used to normalize the amount of phosphorylated STAT1 over total STAT1.
Specifications
| Application |
Cell Signaling
|
|---|---|
| Brand |
HTRF
|
| Detection Modality |
HTRF
|
| Molecular Modification |
Total
|
| Product Group |
Kit
|
| Sample Volume |
16 µL
|
| Shipping Conditions |
Shipped in Dry Ice
|
| Target Class |
Phosphoproteins
|
| Target Species |
Human
Mouse
|
| Technology |
TR-FRET
|
| Therapeutic Area |
Infectious Diseases
Neuroscience
Oncology & Inflammation
|
| Unit Size |
10,000 Assay Points
|
Video gallery
HTRF Human & Mouse Total STAT1 Detection Kit, 10,000 Assay Points
HTRF Human & Mouse Total STAT1 Detection Kit, 10,000 Assay Points
How it works
Total-STAT1 assay principle
The Total-STAT1 assay quantifies the expression level of STAT1 in a cell lysate. Contrary to Western Blot, the assay is entirely plate-based and does not require gels, electrophoresis or transfer. The Total-STAT1 assay uses two labeled antibodies: one coupled to a donor fluorophore, the other to an acceptor. Both antibodies are highly specific for a distinct epitope on the protein. In presence of STAT1 in a cell extract, the addition of these conjugates brings the donor fluorophore into close proximity with the acceptor and thereby generates a FRET signal. Its intensity is directly proportional to the concentration of the protein present in the sample, and provides a means of assessing the proteins expression under a no-wash assay format.
Total-STAT1 2-plate assay protocol
The 2 plate protocol involves culturing cells in a 96-well plate before lysis then transferring lysates to a 384-well low volume detection plate before adding Total-STAT1 HTRF detection reagents. This protocol enables the cells' viability and confluence to be monitored.
Total-STAT1 1-plate assay protocol
Detection of total STAT1 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.
Assay validation
HTRF assay compared to Western Blot using total STAT1 cellular assays on human jurkat cells
HeLa cells were grown in a T175 flask at 37 °C, 5% CO2 for 48h. Cells were then stimulated with IFNa for 20 min. After medium removal, the cells were lysed with 3mL of supplemented lysis buffer for 30 min at room temperature. Soluble fractions were then collected after 10 min centrifugation. Serial dilutions of the cell lysate were performed in the supplemented lysis buffer and 16 µL of each dilution were dispensed and analyzed side-by-side by Western-blot and by HTRF. For each cell density tested, the fluorescence ratio closely matched the western blot band intensity, demonstrating the reliability of HTRF as an analytical technique for the measurement of total STAT1.
HTRF total-STAT1 assay used to check the phosphorylation status of STAT1 on murine and human cells
After 20 minutes of stimulation with increasing IFNa concentrations, NIH 3T3 & Hela cells (200,000 cells/96well plate) were lysed with 50 µL of supplemented lysis buffer and incubated for 30 min at RT under gentle shaking. For phospho- STAT1 detection (blue curve), 16 µL of lysate were transferred into a 384-well low volume white microplate, followed by 4 µL of the HTRF phospho-STAT1 detection reagents For total STAT1 detection (red curve), 16µl of lysate were transferred into a 384-well low volume white, followed by 4 µL of the HTRF Total-STAT1 detection reagents. HTRF signals were recorded after an overnight incubation. Note that the HeLa cells display better potency of IFNa compared to NIH3T3 cells.
Simplified pathway
Transcriptional activator STAT1 involved in the JAK/STAT pathway
STAT1 is an important transcriptional activator involved in the JAK/STAT pathway which is activated by interferon I class, growth factors or chemokines. After stimulation, phosphorylated STAT1 dimers bind to Interferon Stimulated Gene Factor 3 complex. Then STAT1 proteins translocate into the nucleus and activate the transcription of genes associated to cell survival, viability or pathogen response. In response to IFNγ, STAT1 forms homodimers or heterodimers with STAT3 that bind to the GAS (Interferon-Gamma-Activated Sequence) promoter element. In response to either IFNα or IFNß, STAT1 forms heterodimer with STAT2 that bind the Interferon-Stimulated Response Element (ISRE).
Resources
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Application Note
Neuroinflammation study combining hiPSC-derived astrocytes and HTRF
Dive deeper into astrocyte cell research
The release of pro-inflammatory factors by activated astrocytes has been shown to be...
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