Rat PAPPA(Pregnancy Associated Plasma Protein A) ELISA Kit

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  • sandwich-Ab-ELISA-Elabscience
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    • sandwich-Ab-ELISA-Elabscience
    • sandwich-Ab-ELISA-Elabscience
    • sandwich-Ab-ELISA-Elabscience
    • sandwich-Ab-ELISA-Elabscience
    • sandwich-Ab-ELISA-Elabscience
    • sandwich-Ab-ELISA-Elabscience

      Catalog number:E-EL-R0056

      Synonyms:PAPP-A, PAPA, DIPLA1, IGFBP-4ase, PAPPA1, ASBABP2, Pappalysin 1

      Size:
      • 96T
      Qty:
      - +
      Price: $580

      Reactivity: Rat

      Detection Range: 0.16~10 ng/mL

      Sensitivity: 0.10 ng/mL

      Lead Time: 7~10 daysWelcome to order from local distributors.

      Add to cart Compare Bulk request Manual

      Intended use

      This ELISA kit applies to the in vitro quantitative determination of Rat PAPPA concentrations in serum, plasma and other biological fluids.

      Test principle

      This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat PAPPA. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat PAPPA and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Rat PAPPA, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat PAPPA. You can calculate the concentration of Rat PAPPA in the samples by comparing the OD of the samples to the standard curve.

      Assay type Sandwich-ELISA
      Format 96T
      Assay time 4.5h
      Reactivity Rat
      Detection Method Colormetric
      Detection Range 0.16—10 ng/mL
      Sensitivity 0.10 ng/mL
      Sample Volume Required Per Well 100μL
      Sample Type Serum, plasma and other biological fluids

      Specificity

      This kit recognizes Rat PAPPA in samples. No significant cross-reactivity or interference between Rat PAPPA and analogues was observed.

      Typical data

      As the OD values of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.

      Concentration
      (ng/mL)
      O.D Average Corrected
      10 2.425
      2.465
      2.445 2.368
      5 1.647
      1.671
      1.659 1.582
      2.5 0.918
      0.894
      0.906 0.829
      1.25 0.48
      0.484
      0.482 0.405
      0.63 0.266
      0.238
      0.252 0.175
      0.31 0.185
      0.165
      0.175 0.098
      0.16 0.125
      0.133
      0.129 0.052
      0 0.077
      0.077
      0.077 --

      Precision

      Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Rat PAPPA were tested 20 times on one plate, respectively.
      Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Rat PAPPA were tested on 3 different plates, 20 replicates in each plate.

      Intra-assay Precision Inter-assay Precision
      Sample 1 2 3 1 2 3
      n 20 20 20 20 20 20
      Mean (ng/mL) 0.50 1.50 3.40 0.50 1.40 3.50
      Standard deviation 0.03 0.06 0.17 0.03 0.06 0.12
      C V (%) 6.00 4.00 5.00 6.00 4.29 3.43

      Recovery

      The recovery of Rat PAPPA spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.

      Sample Type Range (%) Average Recovery (%)
      Serum (n=5) 87-99 92
      EDTA plasma (n=5) 93-110 101
      Cell culture media (n=5) 87-100 94

      Linearity

      Samples were spiked with high concentrations of Rat PAPPA and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.

      Serum (n=5) EDTA plasma (n=5) Cell culture media (n=5)
      1:2 Range (%) 93-107 91-103 95-107
      Average (%) 100 97 100
      1:4 Range (%) 97-108 84-95 95-111
      Average (%) 102 89 102
      1:8 Range (%) 94-110 87-101 95-110
      Average (%) 100 94 103
      1:16 Range (%) 96-113 86-97 97-110
      Average (%) 103 91 103

      Kit components & Storage

      An unopened kit can be stored at 4℃ for 1 month. If the kit is not used within 1 month, store the items separately according to the following conditions once the kit is received.

      Item Specifications Storage
      Micro ELISA Plate(Dismountable) 8 wells ×12 strips -20℃, 6 months
      Reference Standard 2 vials
      Concentrated Biotinylated Detection Ab (100×) 1 vial, 120 μL
      Concentrated HRP Conjugate (100×) 1 vial, 120 μL -20℃(shading light), 6 months
      Reference Standard & Sample Diluent 1 vial, 20 mL 4℃, 6 months
      Biotinylated Detection Ab Diluent 1 vial, 14 mL
      HRP Conjugate Diluent 1 vial, 14 mL
      Concentrated Wash Buffer (25×) 1 vial, 30 mL
      Substrate Reagent 1 vial, 10 mL 4℃(shading light)
      Stop Solution 1 vial, 10 mL 4℃
      Plate Sealer 5 pieces
      Product Description 1 copy
      Certificate of Analysis 1 copy

      Note: All reagent bottle caps must be tightened to prevent evaporation and microbial pollution.
      The volume of reagents in partial shipments is a little more than the volume marked on the label, please use accurate measuring equipment instead of directly pouring into the vial(s).

      Other supplies required

      • Microplate reader with 450 nm wavelength filter
      • High-precision transfer pipette, EP tubes and disposable pipette tips
      • Incubator capable of maintaining 37℃
      • Deionized or distilled water
      • Absorbent paper
      • Loading slot for Wash Buffer

      Assay Procedure

      1.Add 100 μL standard or sample to each well. Incubate for 90 min at 37℃.

      2.Remove the liquid.

      3.Add 100 μL Biotinylated Detection Ab. Incubate for 1 hour at 37℃. Aspirate and wash 3 times.

      4.Add 100 μL HRP Conjugate. Incubate for 30 min at 37℃. Aspirate and wash 5 times.

      5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.

      6.Add 50 μL Stop Solution.

      7.Read at 450 nm immediately. Calculation of results.

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