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KLH IgM ELISA Kit

KLH IgM Reaktivität: Affe Colorimetric Sandwich ELISA Plasma, Serum
Produktnummer ABIN956291
  • Target Alle KLH IgM Produkte
    KLH IgM (Anti-Keyhole Limpet Hemocyanin IgM Antibody (KLH IgM))
    Reaktivität
    • 1
    • 1
    • 1
    Affe
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Applikation
    ELISA
    Proben
    Plasma, Serum
    Analytische Methode
    Quantitative
    Produktmerkmale
    The Monkey Anti-KLH IgM ELISA is based on a solid phase enzyme-linked immunosorbent assay (ELISA). The assay uses KLH for solid phase (microtiter wells) immobilization and horseradish peroxidase (HRP) conjugated goat anti- monkey IgM antibodies for detection. Test serum or plasma samples are diluted and incubated in the microtiter wells for 45 minutes. The microtiter wells are subsequently washed and HRP conjugate is added and incubated for 45 minutes. Anti-KLH IgM molecules are thus sandwiched between immobilized KLH and the detection antibody conjugate. The wells are then washed to remove unbound HRP-labeled antibodies and TMB reagent is added and incubated for 20 minutes at room temperature. This results in the development of a blue color. Color development is stopped by the addition of stop solution, changing the color to yellow, and optical density is measured spectrophotometrically at 450 nm. The concentration of anti-KLH IgM is proportional to the optical density of the test sample.
    Bestandteile
    Microtiter Plate: KLH coated 96-well plate (12 strips of 8 wells)
    Enzyme Conjugate Solution: 11 mL
    Calibrator: Lyoph.
    Diluent Buffer: 50 mL
    TMB Solution: 11 mL
    Stop Solution: 11 mL, 1N HCl
    Wash Buffer (20x): 50 mL.
    Benötigtes Material
    Plate reader (450 nm)
    Micropipette and tips
    De-ionized water
    Graph paper (PC software is optional)
    Paper towels
    Polypropylene or glass tubes
    Vortex mixer
    Plate shaker/incubator
    Plate washer.
  • Plattentyp
    Pre-coated
    Aufbereitung der Reagenzien

    Wash Buffer: The wash solution is provided as 20x stock. Prior to use dilute the contents of the bottle (50 mL) with 950 mL of distilled of deionized water. Diluent The diluent is provided as 10x stock. Prior to use estimate the final volume of diluent required for your assay and dilute one volume of the 10x stock with nine volumes of distilled or deionized water. Calibrator
    1. Working 400-12.5 ng/mL anti-KLH IgM calibrators should be used within 1 hour of preparation.
    2. The Monkey anti-KLH IgM calibrator is provided as lyophilized stock. Reconstitute as directed on vial label. The reconstituted calibrator should be frozen and stored at -20°C after reconstitution if future use is intended.
    3. Label 6 polypropylene or glass tubes as 400, 200, 100, 50, 25, and 12.5 ng/mL.
    4. Into the tube labeled 400 ng/mL, pipette the volume of diluent detailed on the anti-KLH IgM calibration vial label. Then add the indicated volume of anti-KLH IgM calibrator (shown on the anti-KLH IgM calibrator vial label) and mix gently. This provides the 400 ng/mL calibrator.
    5. Dispense 200 µL of diluent into the tubes labelled 200, 100, 50, 25, and 12.5 ng/mL.
    6. Prepare a 200 ng/mL calibrator by diluting and mixing 250 µL of the 400 ng/mL calibrator with 250 µL of diluent in the tube labelled 200 ng/mL.
    7. Similarly prepare the 100, 50, 25, and 12.5 ng/mL calibrators by serial dilution.

    Aufbereitung der Proben

    Note: The optimal sample dilution should be determined empirically. However, studies indicate that a 500-fold dilution is a reasonable starting point. In order to achieve high dilutions we suggest that a serial dilution strategy be used. If, for example, a 500-fold sample dilution is desired the following procedure should be used. This approach minimizes diluent usage and favors accurate and precise sample dilution.
    1. Dispense 48 µL and 237.5 µL of diluent into separate tubes.
    2. Pipette and mix 2 µL of the serum/plasma sample into the tube containing 48 µL of diluent. This provides a 25 fold diluted sample.
    3. Mix 12.5 µL of the diluted sample with 237.5 µL of diluent in the second tube. This provides a 500 fold dilution of the sample.
    4. Repeat this procedure for each sample to be tested.
    5. Do not use dilutions lower than 100-fold.

    Testdurchführung
    1. Secure the desired number of coated wells in the holder.
      2. Dispense 100 µL of calibrators and diluted samples into the wells (we recommend that samples be tested in duplicate).
      3. Incubate on an orbital micro-plate shaker at 100-150 rpm at room temperature (18-25°C) for 45 minutes.
      4. Aspirate the contents of the microtiter wells and wash the wells 5 times with 1x wash solution using a plate washer (400 µL/well). The entire wash procedure should be performed as quickly as possible.
      5. Strike the wells sharply onto absorbent paper or paper towels to remove all residual wash buffer.
      6. Add 100 µL of enzyme conjugate reagent into each well.
      7. Incubate on an orbital micro-plate shaker at 100-150 rpm at room temperature (18-25°C) for 45 minutes.
      8. Wash as detailed in 4 and 5 above.
      9. Dispense 100 µL of TMB reagent into each well.
      10. Gently mix on an orbital micro-plate shaker at 100-150 rpm at room temperature for 20 minutes.
      11. Stop the reaction by adding 100 µL of Stop Solution to each well.
      12. Gently mix. It is important to make sure all the blue color changes to yellow.
      13. Read the optical density at 450 nm with a microtiter plate reader within 5 minutes.
    Ergebnisberechnung
    1. Calculate the average absorbance values for each set of calibrators and samples.
      2. Construct a calibration curve by plotting the mean absorbance obtained from each calibrator against its concentration in ng/mL on linear graph paper, with absorbance values on the vertical or Y axis and concentrations on the horizontal or X axis.
      3. Using the mean absorbance value for each sample, determine the corresponding concentration of anti-KLH IgM in ng/mL from the calibration curve.
      4. Multiply the derived concentrations by the dilution factor to determine the actual concentration for anti-KLH IgM in the serum/plasma sample.
      5. PC graphing software may be used for the above steps.
      6. If the OD values of samples fall outside the calibration curve samples should be diluted appropriately and re- tested.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4°C. Calibrators should be stored at -20°C. Microtiter plate should be kept in a sealed bag with desiccant to minimize exposure to damp air. Do not freeze HRP conjugate or TMB solutions. The kit is stable until the expiration date when stored as noted in this section.
    Haltbarkeit
    The expiry date is stated on the label.
  • Target Alle KLH IgM Produkte
    KLH IgM (Anti-Keyhole Limpet Hemocyanin IgM Antibody (KLH IgM))
    Andere Bezeichnung
    Keyhole Limpet Heomcyanin (KLH) IgM (KLH IgM Produkte)
    Substanzklasse
    Antibody, Antibody
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