| Field | Specification |
|---|---|
| Mfr No | |
| Accession Number | |
| Alternative Names | PRB2; PRPPRB1; Ps; cP7; proline-rich protein BstNI; subfamily-2 (parotid size variant); salivary proline-rich protein 2 |
| Assay Time | |
| Assay Type | |
| Detection Method | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | Cell culture supernatants, Serum, Plasma, Other biological fluids |
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Features & Benefits
Human Basic salivary proline-rich protein 2 (PRB2) ELISA Kit has high sensitivity and excellent specificity for detection of Human PRB2. No significant cross-reactivity or interference between Human PRB2 and analogues was observed.
Background
The Ps proteins of saliva are so called because they are parotid size variants, i.e., variants in the size of parotid salivary protein. The polymorphism is determined by 1 unexpressed and 2 expressed alleles at an autosomal locus. The electrophoretic polymorphism is manifested by apparent differences in molecular weights between the Ps proteins which are glycosylated. Ps and Pm are closely linked to Pr, Pa, Db, and G1.
Goodman and Karn (1983) presented evidence supporting the conclusion of Azen and Denniston (1980) that there is a molecular weight difference between the 2 allelic proteins Ps-1 and Ps-2. The difference appears to be due to an extension of the Ps-2 chain (presumably at its COOH-end). Minaguchi et al. (1988) described new variants.
This Basic salivary proline-rich protein 2 (PRB2) 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 Basic salivary proline-rich protein 2 (PRB2) 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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