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Anti-Endothelin-Receptor-B IgG Antibody Kit ELISA

Reactivité: Humain Colorimetric Competition ELISA Cell Culture Supernatant, Plasma, Serum
N° du produit ABIN1068572
  • Antigène
    Anti-Endothelin-Receptor-B IgG Antibody
    Reactivité
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Competition ELISA
    Application
    ELISA
    Fonction
    The anti-Endothelin Receptor B Antibody-EIA is designed for the determination of antibodies (IgG) against the Endothelin receptor subtype B in serum and plasma.
    Type d'échantillon
    Serum, Plasma, Cell Culture Supernatant
    Analytical Method
    Quantitative
    Attributs du produit
    The CellTrend anti-Endothelin Receptor B- Antibody-EIA is an antibody screening test.
    Ingrédients
    MTP Microplate strips, Endothelin Receptor B coated: 12 x 8
    Wash buffer, 10fold conc. : 50 ml
    Diluent sample, ready to use : 50 ml
    Diluent conjugate, ready to use : 14 ml
    Standards, ready to use [2.5 - 5 - 10 - 20 - 40 U/ml] : 1 ml
    Positive control, ready to use : 1 ml
    Negative control, ready to use : 1 ml
    anti-human-IgG, HRP conjugate, 100fold conc.: 0,2 ml
    TMB substrate, ready to use: 12 ml
    Stop solution, ready to use (0.5 M sulphuric acid): 12 ml
    Matériel non inclus
    Deionized or distilled water, Graduated cylinder, Micropipettes, multipipette, Microplate reader
  • Plaque
    Pre-coated
    Protocole
    Endothelin- receptor B has been pre-coated onto a microtiter plate. During the first incubation the anti-Endothelin receptor B- Antibodies of the samples are immobilised on the plate. The autoantibodies are detected with a POD labeled anti-human IgG antibody. In the following enzymatic substrate reaction the intensity of the colour correlates with the concentration and/ or avidity of anti-Endothelin receptor B- antibody.
    Préparation des réactifs

    Bring all reagents to room temperature before use. If crystals have formed, mix gently until the crystals have completely dissolved.
    The microplate strips MTP are ready to use. Remove excess strips (breakable) from the frame, reseal in the bag with the desiccant and store at 2-8 °C.
    Dilute the wash buffer BUF│WASH│10x with deionized or distilled water 1:10 (e. g. 50 ml + 450 ml water). The diluted solution is stable for 30 days at 2-8 °C.
    Dilute the HRP conjugate CONJ│ENZ 100x with diluent DIL│Conj 1:100 (e. g. 50 µl + 4950 µl diluent DIL│Conj). The required amount of conjugate solution should be prepared freshly.
    Dilute the human serum or plasma samples with diluent DIL│SPE 1:100 (e. g. 5 µl + 495 µl diluent). Store undiluted samples at
    20 °C.
    Standards CAL│1-5, positive control CONTROL│+, negative control CONTROL│-, the diluent sample DIL│SPE and the diluent conjugate DIL│Conj, are ready to use. Assay procedure It is recommended that all samples and standards be assayed in duplicate. 1. Prepare all reagents and samples as directed in the previous section. 2. Pipette 100 µl of diluted samples, standards, controls or diluent DIL│SPE (as blank) into the wells. 3. Seal wells with adhesive strip and incubate for 2 hour at 4°C temperature. 4. Aspirate fluid from wells and wash three times with 300 µl wash buffer. After the last wash, invert the plate and tap on a clean paper towel. 5. Dispense 100 µl of diluted HRP conjugate into each well 6. Seal wells with adhesive strip and incubate for 1 hour (with shaking) at room temperature. 7. Repeat the wash as in step 4. 8. Dispense 100 µl of TMB substrate SUBS│TMB solution into each well. 9. Incubate for 20 minutes at room temperature in the dark. 10. Add 100 µl of stop solution SOLN│STOP to each well. 11. Determine the absorbance within 30 minutes at 450 nm. A reference wavelength of 620 nm/690 nm is recommended.

    Procédure de l'essai

    Assay procedure summary:
    A. Preparation:
    1. Bring all reagents to room temperature
    2. Dilute wash buffer 1:10
    3. Dilute samples with diluent sample 1:100
    4. Dilute freshly HRP conjugate 1:100 with diluent conjugate
    B. Performance:
    1. Pipette 100 µL of samples, standards, controls into the wells
    2. Incubate for 2 hours at 4°C temperature
    3. Wash three times with 300 µL of wash buffer
    4. Dispense 100 µL of HRP conjugate solution

    5. Incubate for 1 hour (with shaking) at room temperature
    6. Wash three times with 300 µL of wash buffer
    7. Dispense 100 µL of TMB substrate solution
    8. Incubate for 20 minutes at room temperature in the dark
    9. Add 100 µL of stop solution
    10. Measure absorption at 450 nm

    Calcul des résultats

    Create a standard curve using computer software capable of generating a curve fit (four parameter fit, x-axis: linear, anti-ETBR-Ab standard points (2.5 U/ml, 5 U/ml, 10 U/ml, 20 U/ml, 40 U/ml), y-axis: linear, absorbance). The sample concentrations can be calculated from the standard curve. A run is considered valid if the positive control is in the expected range (see label) and the negative control is less than the 10 U/ml. Samples over the standard curve can be assyed again using a higher dilution factor (e.g. 1:500). In this case the concentration read from the standard curve must be multiplied by the additional dilution factor (e.g. 5 for 1:500 dilution).

    Précision du teste
    Intra-assay precision (CV) (n=8) Probe 1 (21.2 U/ml): 4.4% - Inter-assay precision (CV) (n=8) 20.1 U/ml: 3.7%
    Restrictions
    For Research Use only
  • Conseil sur la manipulation
    The assay procedure should be carried out only by qualified and well trained employees. Lipaemic, icteric, haemolysed or microbially contaminated specimen may cause interference. Do not mix reagents from different lots. Some components of the kit contain human blood derivatives. No known test method can offer complete assurance that products derived from human blood will not transmit infectious agents. Therefore, all blood derivatives should be considered potentially infectious. It is recommended that these reagents and human specimens be handled using established good laboratory working practices. Some components of this kit contain Thimerosal, a mercury containing compound. Follow routine precautions for handling hazardous chemicals. Avoid contact with skin and mucous membranes when handling reagents, which contain preservatives (see materials provided). Wash thoroughly with water in case of contact and possibly look up a doctor. The stop solution contains 0.5 M sulphuric acid. Wash thoroughly with water in case of contact with skin. In case of contact with eyes rinse with much water and look up a doctor. Do not allow the wells to become dry once the assay has begun.
    Stock
    4 °C
  • Antigène
    Anti-Endothelin-Receptor-B IgG Antibody
    Classe de substances
    Antibody
    Sujet
    Endothelins (ET) are 21-amino acid vasocon- stricting peptides produced primarily in the endothelium having a key role in vascular homeostasis. It mediates the effects through G-Protein-coupled receptors, the Endothelin receptors. There are two key receptor types, ETA and ETB. ETB is primarily located on the endothelial cells that line the interior of the blood vessels. When endothelin binds to ETB receptors, this leads to the release of nitric oxide, diuresis and mechanisms that lower blood pressure.
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