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Rat D2D(D-Dimer) ELISA Kit

  • Cat.No.:E-EL-R0317

  • Reactivity: Rat

To Purchase E-EL-R0317

Size:
  • 96T
  • 48T
  • 24T
  • 96T*5
  • 96T*10
Price: $609
Qty:

Properties

Format 24T, 48T, 96T, 96T*5, 96T*10
Assay time 2.0h
Sample type plasma
Sample volume 50μL
Sample size Run up to 46 samples in duplicate and 30 samples in triplicate
Storage 2-8℃
Interpretation Detection range: 78.13-5000 ng/mL
Sensitivity: 46.88 ng/mL
Application Quantitative determination of Human concentrations in human serum, plasma and other biological fluids
Reproducibility Both intra-CV and inter-CV are < 10%

Test Principle

This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat D2D. 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 D2D 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 D2D, 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 D2D. You can calculate the concentration of Rat D2D in the samples by comparing the OD of the samples to the standard curve.

Assay Procedures

elisa assay procedure 1

1. Add 50μL standard or sample to the wells, immediately add 50μL Biotinylated Detection Ab working solution to each well. Incubate for 45 min at 37°C

elisa assay procedure 2

2. Aspirate and wash the plate for 3 times

elisa assay procedure 3

3. Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times

elisa assay procedure 4

4. Add 90μL Substrate Reagent. Incubate for 15 min at 37°C

elisa assay procedure 5

5. Add 50μL Stop Solution

elisa assay procedure 6

6. Read the plate at 450nm immediately. Calculation of the results

Citations

  1. THROMBOSIS RESEARCH (2021) IF: 3.944
    Brain-derived extracellular vesicles mediated coagulopathy, inflammation and apoptosis after sepsis

    DOI: 10.1016/j.thromres.2021.09.014

    PMID: 34583153

    Sample: blood
  2. Journal of Comparative Physiology B-Biochemical Systems and Environmental Physiology (2018) IF: 2.517
    Cardiovascular resistance to thrombosis in 13-lined ground squirrels

    DOI: 10.1007/s00360-018-1186-x

    PMID: 30317383

    Sample: plasma

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