Rat Cxc-Chemokine Receptor 2, CXCR2 ELISA Kit
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Chemotactic for human polymorphonuclear leukocytes but does not induce chemokinesis or an oxidative burst. Contributes to neutrophil activation during inflammation.
Fully tested in-house by ABMIUM, or supported by an advanced validation report from a partner reviewed by ABMIUM. Highest confidence. Non-conformities fully supported under the ABMIUM Product Promise.
Quality verified. Independent collaborator or expected-performance data available. Product meets ABMIUM quality standards.
Expected to work based on structural and biochemical data. Not yet directly tested by ABMIUM or a collaborator. No non-conformity support for this combination.
Not recommended for this application or species/sample combination. This may indicate either evidence of unsuitability or that the combination has not been tested and therefore cannot currently be recommended.
Evidence status by application and model.
| Evidence | Serum | Plasma | Cell culture supernatants | Ascites | Tissue homogenates |
|---|---|---|---|---|---|
| Compatibility |
This product is manufactured by BT LAB and sold through ABMIUM without relabelling.
ABMIUM supports global orders. Availability, shipping requirements and applicable import arrangements are confirmed before fulfilment where required.
Yes. Send your target, sample, application and experimental conditions through ABMIUM MATCH or technical support.
Unless the listing expressly states otherwise, ABMIUM products are supplied for research use only and are not for diagnostic or therapeutic use.
C-X-C motif chemokine ligand 2 (CXCL2), also known as GRO-beta and MIP-2a, is an inflammatory CXC chemokine expressed at sites of inflammation. This hub connects verified names and identifiers with ABMIUM catalogue products.
Biological function: C-X-C motif chemokine ligand 2 (CXCL2; GRO-beta/MIP-2a) is a secreted inflammatory chemokine produced by activated monocytes and neutrophils. Reviewed UniProt evidence supports chemokine activity, chemotaxis and inflammatory-response biology, while NCBI notes expression at sites of inflammation.
