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Ovalbumin ELISA Kit

High Sensitivity OVA Reaktivität: Diverse Spezies Colorimetric Sandwich ELISA 78 pg/mL - 5000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Produktnummer ABIN6999439
  • Target Alle Ovalbumin (OVA) ELISA Kits anzeigen
    Ovalbumin (OVA)
    Reaktivität
    • 4
    • 1
    • 1
    • 1
    Diverse Spezies
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Detektionsbereich
    78 pg/mL - 5000 pg/mL
    Untere Nachweisgrenze
    78 pg/mL
    Applikation
    ELISA
    Verwendungszweck
    The kit is a high sensitivity sandwich enzyme immunoassay for in vitro quantitative measurement in various sample types.
    Proben
    Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
    Analytische Methode
    Quantitative
    Spezifität
    This assay has high sensitivity and excellent specificity for detection of Ovalbumin.
    Sensitivität
    28 pg/mL
    Güteklasse
    High Sensitivity
    Bestandteile
    • Pre-coated, ready to use 96-well strip plate, flat buttom
    • Plate sealer for 96 wells
    • Reference Standard
    • Standard Diluent
    • Detection Reagent A
    • Detection Reagent B
    • Assay Diluent A
    • Assay Diluent B
    • Reagent Diluent (if Detection Reagent is lyophilized)
    • TMB Substrate
    • Stop Solution
    • Wash Buffer (30 x concentrate)
    • Instruction manual
    Top Product
    Discover our top product OVA ELISA Kit
  • Probenmenge
    100 µL
    Testdauer
    3 h
    Plattentyp
    Pre-coated
    Protokoll
    1. Prepare all reagents, samples and standards,
    2. Add 100μL standard or sample to each well. Incubate 1 hours at 37 °C,
    3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37 °C,
    4. Aspirate and wash 3 times,
    5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
    6. Aspirate and wash 5 times,
    7. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
    8. Add 50μL Stop Solution. Read at 450nm immediately.
    Aufbereitung der Reagenzien
    1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
    2. Standard - Reconstitute the Standard with 0.5mL of Standard Diluent, kept for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 5,000pg/mL. Prepare 7 tubes containing 0.25mL Standard Diluent and produce a double dilution series. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 5,000pg/mL, 2,500pg/mL, 1,250pg/mL, 625pg/mL, 312pg/mL, 156pg/mL, 78pg/mL, and the last tube with Standard Diluent is the blank as 0pg/mL.
    3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, kept for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
    4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
    5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.

    Note:

    1. Making serial dilution in the wells directly is not permitted.
    2. Prepare standard within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
    3. Detection Reagent A and B are sticky solutions, therefore, slowly pipette them to reduce the volume errors.
    4. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
    5. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
    6. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
    7. Contaminated water or container for reagent preparation will influence the detection result.
    Aufbereitung der Proben
    • It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturationmay occur in these samples, leading to false results. Samples should therefore be stored for a short periodat 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thawcycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged toremove precipitates.
    • If the sample type is not specified in the instructions, a preliminary test is necessary to determinecompatibility with the kit.
    • If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibilityof causing a deviation due to the introduced chemical substance.The recommended dilution factor is for reference only.
    • Please estimate the concentration of the samples before performing the test. If the values are not in therange of the standard curve, the optimal sample dilution for the particular experiment has to be determined.Samples should then be diluted with PBS (pH =7.0-7.2).
    Testpräzision
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
    CV(%) = SD/meanX100
    Intra-Assay: CV < 10%
    Inter-Assay: CV < 12%
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C/-20 ° C
    Informationen zur Lagerung
    1. For unopened kit: All reagents should be stored according to the labels on the vials. The Standard, Detection Reagent A, Detection Reagent B, and 96-well Strip Plate should be stored at -20 °C upon receipt, while the other reagents should be stored at 4 °C.
    2. For opened kits: the remaining reagents must be stored according to the above storage conditions. In addition, please return the unused wells to the foil pouch containing the desiccant and seal the foil pouch with the zipper.
    Haltbarkeit
    6 months
  • Target Alle Ovalbumin (OVA) ELISA Kits anzeigen
    Ovalbumin (OVA)
    Andere Bezeichnung
    Ovalbumin (OVA Produkte)
    Synonyme
    1600019A21Rik ELISA Kit, R86 ELISA Kit, SPI-CI ELISA Kit, Spi10 ELISA Kit, ovalbumin ELISA Kit, NK13 ELISA Kit, Spi12 ELISA Kit, BC052216 ELISA Kit, NK21 ELISA Kit, NK21L1 ELISA Kit, Spi13 ELISA Kit, NK26 ELISA Kit, Spi14 ELISA Kit, AW540195 ELISA Kit, AT2 ELISA Kit, Spi9 ELISA Kit, EID ELISA Kit, SPI3B ELISA Kit, Gm11396 ELISA Kit, OTTMUSG00000000720 ELISA Kit, SERPINB14 ELISA Kit, C76171 ELISA Kit, C76174 ELISA Kit, SPI3C ELISA Kit, SPIC ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 9b ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 6b ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 9f ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 9e ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 9d ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 6e ELISA Kit, ovalbumin (SERPINB14) ELISA Kit, serine (or cysteine) peptidase inhibitor, clade B, member 6c ELISA Kit, Serpinb9b ELISA Kit, Serpinb6b ELISA Kit, Serpinb9f ELISA Kit, Serpinb9e ELISA Kit, Serpinb9d ELISA Kit, Serpinb1-ps1 ELISA Kit, Serpinb6e ELISA Kit, OVAL ELISA Kit, Serpinb6c ELISA Kit
    Substanzklasse
    Virus
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