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RBC IgM ELISA Kit

RBC IgM Reaktivität: Schaf Colorimetric Sandwich ELISA Plasma, Serum
Produktnummer ABIN956281
  • Target
    RBC IgM (Anti-Red Blood Cell IgM (RBC IgM))
    Reaktivität
    Schaf
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Applikation
    ELISA
    Proben
    Plasma, Serum
    Analytische Methode
    Quantitative
    Produktmerkmale
    The Rat Anti-SRBC IgM ELISA is based on a solid phase enzyme-linked immunosorbent assay (ELISA). The assay uses detergent solubilized SRBC ghosts for solid phase (microtiter wells) immobilization and horseradish peroxidase (HRP) conjugated anti-rat 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-SRBC IgM molecules are thus sandwiched between immobilized SRBC antigens 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-SRBC IgM is proportional to the optical density of the test sample.
    Bestandteile
    Microtiter Plate: SRBC coated 96-well plate (12 strips of 8 wells)
    Enzyme Conjugate Solution: 11 mL
    Calibrator: Lyoph. x 2
    Diluent Buffer: 30 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. Calibrator
    1. The Rat anti-SRBC IgM calibrator is provided as lyophilized stock. Reconstitute with volume of diluent indicated on the vial label. The reconstituted calibrator is stable at 4°C for one week but should be aliquoted and stored frozen at -20°C after reconstitution if future use is intended.
    2. Label 6 polypropylene or glass tubes as 100, 50, 25, 12.5, 6.25, and 3.125 u/mL, and pipette 250 µL of diluent into each tube.
    3. Into the tube labelled 100 u/mL prepare a 100 u/mL stock by mixing the volume of reconstituted calibrator stock with the volume of diluent detailed on the vial label.
    4. Dispense 250 µL of diluent into the tubes labelled 50, 25, 12.5, 6.25, and 3.125 u/mL.
    5. Prepare a 50 u/mL calibrator by diluting and mixing 250 µL of the 100 u/mL calibrator with 250 µL of diluent in the tube labelled 50 u/mL.
    6. Similarly prepare the 25, 12.5, 6.25, and 3.125 u/mL calibrators by serial dilution.

    Aufbereitung der Proben

    Note: Studies indicate that anti-SRBC IgM is present in rat serum or plasma at concentrations in excess of 4,000 u/mL. In order to obtain values within range of the calibration curve, we suggest samples initially be diluted 200 fold using the following procedure for each sample tested. Optimal dilutions may need to be determined empirically.
    1. For each test sample dispense 298.5 µL of diluent into separate tubes.
    2. Pipette and mix 1.5 µL of the serum/plasma sample into the tube containing 298.5 µL of diluent. This provides a 200 fold diluted sample.
    3. Repeat this procedure for each sample to be tested.
    4. Do not use dilutions lower than 25 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 u/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-SRBC IgM in u/mL from the calibration curve.
      4. Multiply the derived concentrations by the dilution factor to determine the actual concentration for anti-SRBC 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 when tested at a dilution of 100, samples should be diluted appropriately and re-tested.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Handhabung
    Reliable and reproducible results will be obtained when the assay procedure is carried out with a complete understanding of and in accordance with the instructions detailed above.
    The wash procedure is critical. Insufficient washing will result in poor precision and falsely elevated absorbance readings.
    Lagerung
    4 °C
    Informationen zur Lagerung
    Store at 4°C. Microtiter plate should be kept in a sealed bag with desiccant to minimize exposure to damp air. 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
    RBC IgM (Anti-Red Blood Cell IgM (RBC IgM))
    Andere Bezeichnung
    Red Blood Cell (SRBC) IgM
    Substanzklasse
    Antibody, Antibody
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