Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH15-09] to Human IL-29 antibody (Capture) (HA723709) and Recombinant Human IL-29 protein (HA210970) as the standard. The reference range value is 7.8-2,000 pg/mL.
ELISA
Use at an assay dependent concentration.
Target
Function
Cytokine with antiviral, antitumour and immunomodulatory activities. Plays a critical role in the antiviral host defense, predominantly in the epithelial tissues. Acts as a ligand for the heterodimeric class II cytokine receptor composed of IL10RB and IFNLR1, and receptor engagement leads to the activation of the JAK/STAT signaling pathway resulting in the expression of IFN-stimulated genes (ISG), which mediate the antiviral state. Has a restricted receptor distribution and therefore restricted targets: is primarily active in epithelial cells and this cell type-selective action is because of the epithelial cell-specific expression of its receptor IFNLR1. Exerts an immunomodulatory effect by up-regulating MHC class I antigen expression.
Background References
1. Cakmak Genc G et al. Association Between IL28B, IL29 Gene Polymorphisms and Clinical Manifestations of Behcet\'s Disease. Immunol Invest. 2021 Nov
2. Tabari ZA et al. IL29 expression in gingival tissues of chronic periodontitis and aggressive periodontitis patients: An immunohistochemical analysis. Dent Res J (Isfahan). 2021 Aug
Sandwich ELISA analysis of Human IL-29 matched pair antibodies
Capture: HA723709, Human IL-29 Rabbit mAb [PSH15-09] Detector: HA723710, Human IL-29 Rabbit mAb [PSH15-10]
Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA723709) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Human IL-29 protein (HA210970) starting from 2,000 pg/ml to 0 pg/ml and detect antibody (HA723710, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
Interpolated concentrations of native IL-29 in HUVEC cell culture supernatant untreated or treated with Poly(l:C) and IFNα for 24h.
Capture: HA723709, Human IL-29 Rabbit mAb [PSH15-09] Detector: HA723710, Human IL-29 Rabbit mAb [PSH15-10]
Interpolated concentration of native IL-29 was measured in duplicate at different sample concentrations and interpolated from the IL-29 standard curves. The interpolated dilution factor corrected values were plotted (mean +/- SD, n=2). The mean IL-29 concentration was determined to be 202 pg/ml in HUVEC treated cell culture supernatant,undetectable in HUVEC untreated cell culture supernatant.
Interpolated concentrations of spiked IL-29 in cell culture media samples.
Capture: HA723709, Human IL-29 Rabbit mAb [PSH15-09] Detector: HA723710, Human IL-29 Rabbit mAb [PSH15-10]
The concentrations of IL-29 were measured in duplicates, interpolated from the IL-29 standard curves and corrected for sample dilution. Undiluted samples are as follows: cell culture media 50%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2).
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