Anti-Human TNFRSF1A Antibody [B273] with collaborator-tested evidence for ICC/IF.
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Anti-Human TNFRSF1A Antibody [B273] is a research-use antibody from Elabscience for studying TNFRSF1A in IF/ICC workflows with listed reactivity for Human. Specifications and supporting documents below should be reviewed when planning the experiment.
Fully tested in-house 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.
| Species | WB | IHC-P | IHC-Fr | IF/ICC | Flow Cyt | IP | ChIP | ICC/IF |
|---|---|---|---|---|---|---|---|---|
| Human |
This product is manufactured by Elabscience 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.
TNF receptor superfamily member 1A (TNFRSF1A), commonly called TNF receptor 1 (TNFR1) or CD120a, is a receptor for tumor necrosis factor. This ABMIUM record links NCBI Gene 7132 and UniProtKB P19438 to catalogue-backed research products.
Biological function: TNF receptor superfamily member 1A (TNFRSF1A/TNFR1/CD120a) binds TNF and lymphotoxin-alpha. Receptor signalling can activate inflammatory and cell-survival pathways and, through its intracellular death domain and adaptor complexes, can also initiate caspase-dependent apoptosis.
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