The QuickStep Human D2D D-Dimer ELISA Kit is a highly sensitive and specific assay designed for the accurate measurement of D-dimer levels in human samples including serum and plasma. D-dimer is a fibrin degradation product that serves as a biomarker for various medical conditions, particularly in the diagnosis and monitoring of thrombotic disorders such as deep vein thrombosis, pulmonary embolism, and disseminated intravascular coagulation.
With its reliable and reproducible results, this ELISA kit is ideal for researchers and healthcare professionals looking to study thrombotic diseases, assess coagulation status, and monitor treatment effectiveness. Understand and quantify D-dimer levels with precision using the QuickStep Human D2D D-Dimer ELISA Kit.
Product Name:
QuickStep Human D-Dimer ELISA Kit
Product Code:
QSES024
Assay Type:
Sandwich
Assay Format:
96T
Assay Time:
1.5h
Reactivity:
Human
Sensitivity:
53.10 pg/mL
Range:
125.00-4000 pg/mL
Detection Method:
Colormetric
Sample Type:
Serum and plasma
Target:
D2D
Application:
This ELISA kit applies to the in vitro quantitative determination of D2D concentrations in serum and plasma.
Specificity:
This kit recognizes D2D in samples. No significant cross-reactivity or interference between D2D and analogues was observed.
Dilution Method:
It is recommended to dilute normal plasma samples at 20-50 fold.
Reproducibility:
Both intra-CV and inter-CV are < 10%.
Storage & Stability:
An unopened kit can be stored at 2-8°C for 6 months. After test, the unused wells and reagents should be stored according to the storage table in the manual.
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 Human D2D. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human D2D are added to the micro ELISA plate wells. Human D2D in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human D2D. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. 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 ± 2 nm. The OD value is proportional to the concentration of Human D2D. The concentration of Human D2D in the samples is then determined by comparing the OD of the samples to the standard curve.
Item
Specifications
Storage
Micro ELISA Plate(Dismountable)
8 wells - 12 strips
2-8°C, 1 months
Reference Standard
2 vials
2-8°C, use the reconstituted standard within 24h
Concentrated HRP Linked Detection Ab(100-)
1 vial, 60 µL
2-8°C(Protect from light)
Reference Standard & Sample Diluent
1 vial, 20 mL
2-8°C
HRP Linked Ab Diluent
1 vial, 14 mL
Concentrated Wash Buffer(25-)
1 vial, 30 mL
Substrate Reagent
1 vial, 10 mL
2-8°C(Protect from light)
Stop Solution
1 vial, 10 mL
2-8°C
Plate Sealer
5 pieces
Product Description
1 copy
Certificate of Analysis
1 copy
Intra-assay Precision
Inter-assay Precision
Sample
1
2
3
1
2
3
n
20
20
20
20
20
20
Mean (pg/mL)
193.00
640.27
1476.29
177.05
587.91
1461.37
Standard deviation
11.04
32.91
53.74
8.89
23.69
47.64
CV (%)
5.72
5.14
3.64
5.02
4.03
3.26
Sample Type
Range (%)
Average Recovery (%)
Serum(n=8)
93-108
100
EDTA plasma(n=8)
90-104
96
Samples were spiked with high concentrations of Human D2D and diluted with Reference Standard & Sample Diluent to produceSamples with values within the range of the assay.
