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Human Interleukin 26,IL-26 ELISA Kit

Product Details

Description

The Human Interleukin 26 (IL-26) ELISA Kit quantitates IL-26 levels in human serum, urine, tissue homogenates, cell lysates, or cell culture supernates. IL-26, a cytokine primarily secreted by Th1 and Th17 cells, belongs to the IL-20 cytokine subfamily. It displays antimicrobial activity. IL-26 also signals through the IL-10R2/IL-20R1 heterodimeric receptor to activate cells via STAT3 phosphorylation. Acting as a potent chemoattractant for neutrophils, IL-26 drives inflammation and activates neutrophils to release inflammatory cytokines, proteases, and antimicrobial peptides. In addition to being a driver of inflammation, IL-26 may also act as an effector of inflammation, leading to the establishment of a deleterious amplification loop and ultimately sustained inflammation.

This kit employs the sandwich-ELISA mechanism in conjugation with IL-26 antibody-IL-26 antigen-specific binding as well as HRP-TMB chromogenic reaction to measure the concentrations of IL-26 in the samples. The kit is characterized by high sensitivity, strong specificity, good linearity, recovery of 93%-107%, precision less than 10%, and lot-to-lot consistency. Refer to the product instructions for more validation information.

Target Name Interleukin 26,IL-26
Alternative Names AK155 ELISA Kit; IL 26 ELISA Kit; IL-26 ELISA Kit; IL26 ELISA Kit; IL26_HUMAN ELISA Kit; Interleukin 26 ELISA Kit; Interleukin-26 ELISA Kit; Protein AK155 ELISA Kit
Abbreviation IL26
Species Homo sapiens (Human)
Sample Types serum, urine, tissue homogenates, cell lysates, cell culture supernates
Detection Range 62.5 pg/mL-4000 pg/mL
Sensitivity 15.6 pg/mL
Assay Time 1-5h
Sample Volume 50-100ul
Detection Wavelength 450 nm
Research Area Immunology
Assay Principle quantitative
Measurement Sandwich
Precision
Intra-assay Precision (Precision within an assay): CV%   
Three samples of known concentration were tested twenty times on one plate to assess.  
Inter-assay Precision (Precision between assays): CV%   
Three samples of known concentration were tested in twenty assays to assess.    
             
Linearity
To assess the linearity of the assay, samples were spiked with high concentrations of human IL-26 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
  Sample Serum(n=4)  
1:1 Average % 96  
Range % 90-102  
1:2 Average % 89  
Range % 84-95  
1:4 Average % 100  
Range % 95-106  
1:8 Average % 97  
Range % 92-104  
Recovery
The recovery of human IL-26 spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.
Sample Type Average % Recovery Range  
Serum (n=5) 89 93-96  
EDTA plasma (n=4) 102 98-107  
             
             
Typical Data
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
pg/ml OD1 OD2 Average Corrected  
4000 2.749 2.798 2.774 2.616  
2000 2.315 2.364 2.340 2.182  
1000 1.843 1.889 1.866 1.708  
500 1.399 1.381 1.390 1.232  
250 0.899 0.888 0.894 0.736  
125 0.483 0.487 0.485 0.327  
62.5 0.316 0.329 0.323 0.165  
0 0.157 0.159 0.158    
Materials provided
  • A micro ELISA plate --- The 96-well plate has been pre-coated with an anti-human IL-26 antibody. This dismountable microplate can be divided into 12 x 8 strip plates.
  • Two vials lyophilized standard --- Dilute a bottle of the standard at dilution series, read the OD values, and then draw a standard curve.
  • One vial Biotin-labeled IL-26 antibody (100 x concentrate) (120 μl/bottle) ---Act as the detection antibody.
  • One vial HRP-avidin (100 x concentrate) (120 μl/bottle) --- Bind to the detection antibody and react with the TMB substrate to make the solution chromogenic.
  • One vial Biotin-antibody Diluent (15 ml/bottle) ---Dilute the Biotin-antibody solution.
  • One vial HRP-avidin Diluent (15 ml/bottle) ---Dilute the HRP-avidin solution.
  • One vial Sample Diluent (50 ml/bottle)---Dilute the sample to an appropriate concentration.
  • One vial Wash Buffer (25 x concentrate) (20 ml/bottle) --- Wash away unbound or free substances.
  • One vial TMB Substrate (10 ml/bottle) --- Act as the chromogenic agent. TMB interacts with HRP, eliciting the solution turns blue.
  • One vial Stop Solution (10 ml/bottle) --- Stop the color reaction. The solution color immediately turns from blue to yellow.
  • Four Adhesive Strips (For 96 wells) --- Cover the microplate when incubation.
  • An instruction manual
Materials not provided
  • A microplate reader capable of measuring absorbance at 450 nm, with the correction wavelength set at 540 nm or 570 nm.
  • An incubator that can provide stable incubation conditions up to 37°C±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.
  • Adjustable pipettes to measure volumes ranging from 2 µL to 1 mL and pipette tips.
  • Timer
  • Test tubes for dilution.
Storage Store at 2-8°C. Please refer to protocol.
Lead Time 3-5 working days
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