| Field | Specification |
|---|---|
| Mfr No | |
| Accession Number | |
| Alternative Names | TNFAIP8L2; RP11-68I18.4; FLJ23467; TIPE2; inflammation factor 20 |
| Assay Time | |
| Assay Type | |
| Detection Method | |
| Gene ID | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | Cell culture supernatants, Serum, Plasma, Other biological fluids |
| Shipping | |
| Storage |
Features & Benefits
Human Tumor necrosis factor alpha-induced protein 8-like protein 2 (TNFAIP8L2) ELISA Kit has high sensitivity and excellent specificity for detection of Human TNFAIP8L2. No significant cross-reactivity or interference between Human TNFAIP8L2 and analogues was observed.
Background
Sun et al. (2008) cloned mouse Tnfaip8l2, which they called Tipe2, and by database analysis, they identified human TNFAIP8L2. The deduced 184-amino acid human protein shares 94% identity with mouse Tnfaip8l2, shares 53% identity with human TNFAIP8 , and contains a death effector domain (DED) and 6 putative alpha-helices characteristic of DED-containing proteins. Northern blot analysis detected strong expression in mouse thymus, spleen, lymph node, and small intestine, with weak expression in lung, skin, and colon. Tnfaip8l2 was also expressed in murine lymphoid cells and cell lines, in inflamed mouse spinal cord, and in TNF-alpha-stimulated mouse fibroblasts, suggesting that Tnfaip8l2 is preferentially expressed in lymphoid tissue.
This Tumor necrosis factor alpha-induced protein 8-like protein 2 (TNFAIP8L2) ELISA kit is validated for use with Cell culture supernatants, Serum, Plasma, Other biological fluids. Samples should be collected, processed, and stored correctly to preserve analyte integrity — avoid repeated freeze-thaw cycles and centrifuge to remove particulates before use. Dilute samples exceeding the kit's detection range using the supplied assay diluent. Hemolytic, icteric, or lipemic samples may affect assay performance and should be tested with caution.
This is a sandwich ELISA kit employing an HRP (horseradish peroxidase)-conjugated secondary antibody paired with a TMB (3,3′,5,5′-tetramethylbenzidine) colorimetric substrate. In the sandwich format, the target analyte Tumor necrosis factor alpha-induced protein 8-like protein 2 (TNFAIP8L2) captured on the microplate surface is detected by the conjugated antibody, generating a colorimetric signal proportional to analyte concentration. The reaction is stopped and absorbance measured at 450 nm on a standard microplate reader.
The complete protocol, from sample addition to final plate reading, requires approximately 3–5 hours. This includes two incubation periods (analyte binding and detection antibody steps), intermediate wash cycles to remove unbound material, 15–30 minutes of TMB substrate development, and final stop-solution addition before absorbance reading. Exact timing will vary with experience level and the number of samples processed in parallel.
Required equipment: (1) a microplate spectrophotometer capable of reading absorbance at 450 nm (reference wavelength 540–570 nm recommended for background correction); (2) precision single-channel or multichannel pipettes; (3) a plate washer or multichannel aspirator; (4) a microcentrifuge for sample clarification; and (5) a 37°C incubator or stable room-temperature environment. No fluorescence or luminescence reader is required — standard colorimetric plate readers are fully compatible with this kit.
This ELISA kit is formally validated for Human. Cross-reactivity with species not listed in the specification has not been independently characterized. Variability in protein sequence homology across species means that performance in unlisted species cannot be guaranteed without additional validation. For cross-species detection requirements or non-standard sample matrices, please contact BioHippo support or refer to the manufacturer's technical team for guidance.
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