Human IL12B / NKSF2 / p40 ELISA Pair Set

Details zu Produkt Nr. ABIN2010398, Anbieter: Anmelden zum Anzeigen
Protein- /Substanz
  • CLMF
  • CLMF2
  • IL-12B
  • NKSF
  • NKSF2
  • p40
  • Il-12b
  • Il12p40
  • Il-12p40
  • Il12
  • IL-12p40
  • IL-12
  • IL-12 p40
  • il12b
  • il12p40.b
  • zgc:152789
  • IL-12.p40
  • IL12p40
  • IL12B
  • CLMF p40
  • interleukin 12B
  • interleukin 12A
  • interleukin 12b
  • interleukin 12Ba
  • IL12B
  • IL12A
  • Il12b
  • il12ba
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Verwendungszweck 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 ahorseradish peroxidase conjugated rabbit anti-IL12B monoclonal antibody is then added, producing an antibody-antigen-antibody "sandwich". The wells are again washed and TMB substrate solution is loaded, which produces colorin proportion to the amount of IL12B (NKSF2 / p40) present in the sample. To end the enzyme reaction, the stopsolution is added and absorbances of the microwell are read at 450 nm.
Sensitivität The minimum detectable dose of human IL12B ( NKSF2 / p40 ) was determined to be approximately 7.8125 pg/mL. This is defined as at least three times standard deviations above the mean optical density of 10 replicates of the zero standard.
Produktmerkmale Pair Set
Bestandteile Capture Antibody - 0.5 mg/mL of mouse anti-IL12B monoclonal antibody. Dilute to a workingconcentration of 2.0 μg/mL in CBS before coating.
Detection Antibody - 0.4 mg/mL biotinylated rabbit anti-IL12B monoclonal antibody. Dilute toworking concentration of 0.5 μg/mL in detection antibody diluteion buffer before use.
Standard - Each vial contains 9 ng of recombinant IL12B. Reconstitute standard powder with 1mLdetection antibody dilution buffer. After reconstitution, store at -20 °C to -70 °C in a manual defrostfreezer. A seven-point standard curve using 2-fold serial dilutions in sample dilution buffer, and ahigh standard of 500 pg/mL is recommended.
Benötigtes Material 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
Andere Bezeichnung IL12B
Hintergrund Interleukin 12 (IL-12) , also known as NKSF or CLMF, is a disulfide-linked heterodimeric cytokine composed of a 35 kDasubunit P35 and a 40 kDa subunit P40, also designated as IL-12A and IL-12B. IL-12 is predominantly produced bymacrophages and B lymphocytes and plays an important role in the activities of natural killer cells and T lymphocytes. Itis involved in the differentiation and development of Th1 cells, enhancement of natural killer cells' cytolytic function andmitogenic effects, as well as induction of IFN-gamma during which it can synergize with other IFN-gamma inducers. Alarge excess of monomeric IL-12B is also secreted by the cells producing IL-12, and exhibits no demonstrable biologicalactivity. Overexpression of IL-12B has been shown to be associated with the pathogenesis of multiple sclerosis.
Applikationshinweise Optimal working dilution should be determined by the investigator.

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.

Aufbereitung der Reagenzien
  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.
  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 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.
    6. Add 50 μL of stop solution to each well. Gently tap the plate to ensure thorough mixing.
    7. Determine the optical density of each well immediately, using a microplate reader set to 450 nm.

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.

Beschränkungen Nur für Forschungszwecke einsetzbar
Format Lyophilized
Vorsichtsmaßnahmen The Stop Solution suggested for use with this Pair Set is an acid solution. Wear eye, hand, face, andclothing protection when using this material.
Handhabung Avoid repeated freeze-thaw cycles.
Lagerung 4 °C/-20 °C/-80 °C
Informationen zur Lagerung 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.
Haltbarkeit 6 months
Bilder des Herstellers
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