View All
| Feature | Specification |
|---|---|
| Application | Protein Quantification |
| Dynamic Range | 1.6 - 100,000 pg/mL |
| Limit of Detection | 1.6 pg/mL |
| Sample Volume | 5 µL |
Formats:
Features:
C-X-C Motif Chemokine 9 (CXCL9), previously called MIG, is a 14 kDa protein belonging to the intercrine alpha (chemokine CXC) family. Its induction is enhanced by TNFa in dermal fibroblasts and vein endothelial cells. The synthesis of CXCL9 is specifically induced in macrophages, monocytes, neutrophils, APC, B cells, and eosinophils by IFN? and mediated via the JAK-STAT signaling pathway. The main function of this chemokine is the recruitment of leukocytes to sites of infection and inflammation. Some studies have shown that CXCL9 is active against Gram-negative and Gram-positive bacteria. CXCL9 may play a role as a mediator of T-cell recruitment and activation in some diseases like psoriasis and pulmonary disease. CXCL9 is expressed in allogeneic skin grafts several days before completion of rejection.
AlphaLISA technology allows the detection of molecules of interest in a no-wash, highly sensitive, quantitative assay. In an AlphaLISA assay, a biotinylated anti-analyte antibody binds to the Streptavidin-coated Donor beads while another anti-analyte antibody is conjugated to AlphaLISA Acceptor beads. In the presence of the analyte, the beads come into close proximity. The excitation of the Donor beads causes the release of singlet oxygen molecules that triggers a cascade of energy transfer in the Acceptor beads, resulting in a sharp peak of light emission at 615 nm.
The AlphaLISA assay is based on an AlphaLISA sandwich immunoassay involving a biotinylated anti-analyte antibody bound to Streptavidin-coated AlphaLISA Donor beads and an anti-analyte antibody conjugated to AlphaLISA Acceptor beads. Both antibodies are directed against the analyte of interest. In the presence of the target, both antibodies bind to analyte and the beads come into proximity. The excitation of the Donor beads provokes the release of singlet oxygen molecules that triggers a cascade of energy transfer within the Acceptor beads, resulting in emission with λmax at 615 nm. The intensity of the signal is directly proportional to the concentration of analyte present in the sample.
The AlphaLISA assay can be run in a 96- or 384-well detection plate (50 µL final). As described here, samples or standards are dispensed directly into the assay plate for the detection of the analyte of interest by AlphaLISA reagents. No washing steps are needed. The protocol can be further miniaturized or upscaled by simply resizing each addition volume proportionally.
| Application |
Protein Quantification
|
|---|---|
| Automation Compatible |
Yes
|
| Brand |
AlphaLISA
|
| Detection Modality |
Alpha
|
| Dynamic Range |
1.6 - 100,000 pg/mL
|
| Limit of Detection |
1.6 pg/mL
|
| Product Group |
Kit
|
| Sample Volume |
5 µL
|
| Shipping Conditions |
Shipped in Blue Ice
|
| Target |
CXCL9
|
| Target Class |
Cytokines
|
| Target Species |
Human
|
| Technology |
Alpha
|
| Therapeutic Area |
Inflammation
|
| Unit Size |
500 assay points
|
Are you looking for resources, click on the resource type to explore further.
Cytokines play a vital role in both innate and adaptive immunity and are known for their ability to exert diverse functions on...
Advance your autoimmune disease research and benefit from Revvity broad offering of reagent technologies
Loading...
We are here to answer your questions.