Human IL1R1 ELISA Kit, Lot 21AO-1394 [Cancer Immune Checkpoint Assay Kit] (CAT#: IOK-05-P1305)

Microstrips Coated w / Capture Antibody: 12 x 8-Well Microstrips.
Protein Standard: Lyophilized (100 ng), Red container.
Biotinylated Detection Antibody: Lyophilized, Yellow container.
400x Streptavidin-HRP: 30 μL, Blue container.
Wash Buffer (10x): 50 mL, Clear containter.
Assay Diluent: 50 mL, Clear container.
Ready-to-Use Substrate: 12 mL, Brown container.
Stop Solution: 12 mL, Clear container.
Adhesive Plate Sealers: 4 Sheets.
Technical Manual 1 Manual.

Microplate reader capable of measuring absorbance at 450nm, with the correction wavelength set at 540nm or 570nm.
An incubator which can provide stable incubation conditions up to 37°C ± 0.5°C.
Squirt bottle, manifold dispenser or automated microplate washer.
Absorbent paper for blotting the microtiter plate.
100mL and 500mL graduated cylinders.
Deionized or distilled water.
Pipettes and pipette tips.
Test tubes for dilution.

Pre-coated

1.Reconstitute the Biotin-Conjugated Detection Antibody in 67 µL of ddH₂O for a concentration of 180 µg/ml.
2.Reconstitute the Protein Standard in 100 µL of ddH₂O for a concentration of 340 ng/ml.
3.Dilute the 50 mL of 10x Wash Buffer in 450 mL of ddH2O for 500 mL of 1x Wash Buffer.

Average the duplicate readings for each standard, control, and samples and subtract the average zero standard optical density. Construct a standard curve by plotting the mean O.D. and concentration for each standard and draw a best fit curve through the points on the graph or create a standard curve on log-log graph paper with target concentration on the y-axis and absorbance on the x-axis.

Reagents provided in this kit may be harmful if ingested, inhaled or absorbed through the skin. Please carefully review the MSDS for each reagent before conducting the experiment.

The kit should not be used beyond the expiration date on the kit label.
Do not mix or substitute reagents with those from other lots or sources.
If samples generate values higher than the highest standard, dilute the samples with Sample Diluent and repeat the assay.
Any variation in Sample Diluent, operator, pipetting technique, washing technique, incubation time/temperature and kit age can cause variation in binding.
This assay is designed to eliminate interference by soluble receptors, binding proteins and other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded.

4 °C

Unopened Kits: Store at 4 °C for 6 months.

6 months

Unopened Kits: Store at 4 °C for 6 months.

For Research Use only

Interleukin 1 Receptor Type I (IL1R1)

CD121A; D2S1473; IL-1R-alpha; IL1R; IL1RA; P80; CD121a; CD121b; IL-iR; Il1r-1; interleukin 1 receptor type 1; interleukin 1 receptor; type I; IL1R1; Il1r1

The Human IL-1sRI (interleukin 1 soluble receptor I) ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of human IL-1sRI in serum, plasma, cell culture supernatants and urine.

3554

P14778

NF-kappaB Signaling, Carbohydrate Homeostasis, Cancer Immune Checkpoints

This particular immunoassay utilizes the quantitative technique of a Sandwich Enzyme-Linked Immunosorbent Assay (ELISA) where the target protein (antigen) is bound in a sandwich format by the primary capture antibodies coated to each well-bottom and the secondary detection antibodies added subsequently by the investigator. The capture antibodies coated to the bottom of each well are specific for a particular epitope on the Human IL-1 R1 cytokine while the user-added detection antibodies bind to epitopes on the captured target protein. After incubation and sandwiching of the target antigen, a peroxidase enzyme is conjugated to the constant heavy chain of the secondary antibody, allowing for a colorimetric reaction to ensue upon substrate addition. When the substrate TMB is added, the reaction catalyzed by peroxidase yields a blue color that is representative of the antigen concentration. Upon sufficient color development, the reaction can be terminated through addition of Stop Solution where the color of the solution will turn yellow. The absorbance of each well can then be read by a spectrophotometer, allowing for generation of a standard curve and subsequent determination of protein concentration.