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  • 產(chǎn)品名稱：HumanIL12B/NKSF2/p40ELISAPairSet

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  • 產(chǎn)品廠商：SinoBiological
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HumanIL12B/NKSF2/p40ELISAPairSet
詳情介紹：
Purpose The ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utlizes monoclonal antibody specific for IL12B (NKSF2 / p40) coated on a 96-well plate. Standards and samples are addedto the wells, and any IL12B (NKSF2 / p40) present binds to the immobilized antibody. The wells are washed and abiotinylated rabbit anti- IL12B polyclonal antibody is then added, producing an antibody-antigen-antibody "sandwich". Toproduces color in proportion to the amount of IL12B (NKSF2 / p40) present in the sample strepavidin-HRP and TMBsubstrate solution are loaded. The absorbances of the microwell are read at 450 nm.
Sensitivity The minimum detectable dose of human IL12B ( NKSF2 / p40 ) was determined to be approximately 3.9 pg/mL. This is defined as at least three times standard deviations above the mean optical density of 10 replicates of the zero standard.
Components Capture Antibody - 0.5 mg/mL of mouse anti-IL12B monoclonal antibody. Dilute to a workingconcentration of 1 μg/mL in CBS before coating.
Detection Antibody - Each vial contains 120 μg biotinylated rabbit anti- IL12B polyclonal antibody.Reconstitute with sterile 1 mL distilled water. Dilute to a working concentration of 1.5 μg/mL indetection antibody dilution buffer before use.
Standard - Each vial contains 3 ng of recombinant IL12B. Reconstitute standard powder with 1mLdetection antibody dilution buffer. A seven-point standard curve using 2-fold serial dilutions insample dilution buffer, and a high standard of 250 pg/mL is recommended.
Streptavidin-HRP - 50 μL of streptavidin conjugated to horseradish-peroxidase. 1:2000 Dilution indetection antibody dilution buffer before use.
Material not included CBS - 0.05 M
Na2CO3 - 0.05 M
NaHCO3, pH 9.6, 0.2 μm filtered
TBS - 25 mM
Tris, adjust pH to 7.4 by HCl
Wash Buffer - 0.05 % Tween20 in TBS, pH 7.2 - 7.4
Blocking Buffer - 5 % BSA in Wash Buffer
Sample dilution buffer - 0.5 % BSA in wash buffer, pH 7.2 - 7.4, 0.2 μm filtered
Detection antibody dilution buffer - 0.5 % BSA in wash buffer, pH 7.2 - 7.4, 0.2 μm filtered
Substrate Solution: To achieve best assay results, fresh substrate solution is recommended Substrate stock solution - 10 mg/mL TMB (Tetramethylbenzidine ) in DMSO Substrate dilution buffer - 0.05 M Na2HPO4 and 0.025 M citric acid , adjust pH to 5.5
Substrate working solution - For each plate dilute 250 μL substrate stock solution in 25 mL substrate dilutionbuffer and then add 80 μL 0.75 % H2O2 , mix it well
Stop Solution - 2 N H2SO4
Alternative Name IL12B
Background Interleukin 12 (IL-12) , also known as NKSF or CLMF, is a disulfide-linked heterodimeric cytokine composedof a 35?kDa subunit P35 and a 40?kDa subunit P40, also designated as IL-12A and IL-12B. IL-12 ispredominantly produced by macrophages and B lymphocytes and plays an important role in the activities ofnatural killer cells and T lymphocytes. It is involved in the differentiation and development of Th1 cells, enhancement of natural killer cells' cytolytic function and mitogenic effects, as well as induction of IFN-gamma during which it can synergize with other IFN-gamma inducers. A large excess of monomeric IL-12Bis also secreted by the cells producing IL-12, and exhibits no demonstrable biological activity. Overexpression of IL-12B has been shown to be associated with the pathogenesis of multiple sclerosis.
Research Area Hormones, Cytokines
Application Notes Optimal working dilution should be determined by the investigator.
Comment

The human IL12B ( NKSF2 / p40 ) ELISA Pair Set is for the quantitative determination of human IL12B.This ELISA Pair Set contains the basic components required for the development of sandwich ELISAs.
Reagent Preparation
  1. Dilute the capture antibody to the working concentration in CBS. Immediately coat a 96-well microplate with 100 μL per well of the diluted capture antibody. Seal the plate and incubate overnight at 4 °C.
    2. Aspirate each well and wash with at least 300 μL wash buffer, repeating the process two times for a total of three washes. Complete removal of liquid at each step is essential for good performance. After the last wash, remove any remaining wash buffer by inverting the plate and blotting it against clean paper towels.
    3. Block plates by adding 300 μL of blocking buffer to each well. Incubate at room temperature for a minimum of 1 hour.
    4. Repeat the aspiration/wash as in step 2. The plates are now ready for sample addition.
Assay Procedure
  1. Add 100 μL of sample or standards in sample dilution buffer per well. Seal the plate and incubate 2 hours at roomtemperature.
    2. Repeat the aspiration/wash as in step 2 of plate preparation.
    3. Add 100 μL of the detection antibody, diluted in antibody dilution buffer, to each well. Seal the plate and incubate 1hour at room temperature.
    4. Repeat the aspiration/wash as in step 2 of plate preparation.
    5. Add 100 μL of Streptavidin-HRP to each well. Incubate for 1 hour at room temperature.
    6. Repeat the aspiration/wash as in step 2 of plate preparation.
    7. Add 200 μL of substrate solution to each well. Incubate for 20?minutes at room temperature (if substrate solutionis not as requested, the incubation time should be optimized). Avoid placing the plate in direct light.
    8. Add 50 μL of stop solution to each well. Gently tap the plate to ensure thorough mixing.9. Determine the optical density of each well immediately, using a microplate reader set to 450 nm.
Calculation of Results

Calculate the mean absorbance for each set of duplicate standards, controls and samples. Subtract the mean zero standard absorbance from each. Construct a standard curve by plotting the mean absorbance for each standard on the y-axis against the concentration on the x-axis and draw a best fit curve through the points on the graph. To determine the concentration of the unknowns, find the unknowns' mean absorbance value on the y-axis and draw a horizontal line to the standard curve. At the point of intersection, draw a vertical line to the x-axis and read the concentration. If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor. Alternatively, computer-based curve-fitting statistical software may also be employed to calculate the concentration of the sample.
Restrictions For Research Use only
Precaution of Use The Stop Solution suggested for use with this Pair Set is an acid solution. Wear eye, hand, face, andclothing protection when using this material.
Handling Advice Avoid repeated freeze-thaw cycles.
Storage 4 °C/-20 °C/-80 °C
Storage Comment Capture Antibody: Aliquot and store at -20°C to -80°C for up to 6 months from date of receipt. Detection Antibody: Aliquot and store at -20°C to -80°C for up to 6 months from date of receipt. Standard: Store lyophilized standard at -20°C to -80°C for up to 6 months from date of receipt. Aliquot and store the reconstituted Standard at -80°C for up to 1 month. Streptavidin-HRP: Store at 4°C and protect it from prolonged exposure to light. DO NOT FREEZE! It is stable for up to 6 months from date of receipt.
Expiry Date 6 months
Supplier Images
image for Human IL12B / NKSF2 / p40 ELISA Pair Set (ABIN2010397) Human IL12B / NKSF2 / p40 ELISA Pair Set