| Field | Specification |
|---|---|
| Mfr No | |
| Accession Number | |
| Alternative Names | TNP2; MGC116783; MGC116785; TP2 |
| 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 Nuclear transition protein 2 (TNP2) ELISA Kit has high sensitivity and excellent specificity for detection of Human TNP2. No significant cross-reactivity or interference between Human TNP2 and analogues was observed.
Background
TNP2 were not found in human testicular RNA or human testis cDNA libraries. Finding homologous sequences in the human genome was greatly facilitated, however, by the finding that, in the boar and bull genomes, the genes for protamine-1 (PRM1) and Prm2 are clustered with Tnp2. Schluter et al. (1992) tested a genomic human cosmid clone containing the genes for both protamines and found that the TNP2 gene was within a distance of 7.5 kb 3-prime of the PRM2 gene. The gene was transcribed in human testicular RNA only at a level demonstrable by RT-PCR and RNase protection assay. In contrast to the TNP2 genes of mouse, rat, boar, and bull, the human TNP2 gene lacks the nucleotide sequence GCCATCAC in its 3-prime UTR.
This Nuclear transition protein 2 (TNP2) 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 Nuclear transition protein 2 (TNP2) 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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