D2D ELISA kit (Rat)

SKU: CEA506Ra

Size: 96Tests

# of Times Cited in literature: 5

Prepare Time: 1-3 days(please inquire for mutiple units)

Target Name: D2D

Target Full Name: D-Dimer

Alternative Names: D 2 Dimer

Target Species: Rat

Uniprot: -

Gene ID: -

Featured Series: CE kit

Featured Series Function: Detects small molecule

Specificity: Reactive with Rat D2D / D-Dimer

Method: Colormetric

Detection principle: Competitive Inhibition

Detection range: 61.7-5,000ng/mL

Sensitivity: 22.3ng/mL

Assay Time: 2h

Sample Size: 50uL

Recommended/Predicted Sample Types: Plasma

Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12%

Reproducibility test menthod: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level D-Dimer (D2D) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level D-Dimer (D2D) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100

Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life)

Shelf-life: 12 months

Specificity: This assay has high sensitivity and excellent specificity for detection of D-Dimer (D2D). No significant cross-reactivity or interference between D-Dimer (D2D) and analogues was observed.

Stability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Assay procedure summary: 1. Prepare all reagents, samples and standards; 2. Add 50µL standard or sample to each well. And then add 50µL prepared Detection Reagent A immediately. Shake and mix. Incubate 1 hour at 37°C; 3. Aspirate and wash 3 times; 4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C; 5. Aspirate and wash 5 times; 6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C; 7. Add 50µL Stop Solution. Read at 450 nm immediately.

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to D-Dimer (D2D) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled D-Dimer (D2D) and unlabeled D-Dimer (D2D) (Standards or samples) with the pre-coated antibody specific to D-Dimer (D2D). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of D-Dimer (D2D) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of D-Dimer (D2D) in the sample.

Research Area: Hematology;Cardiovascular biology;

References Citing This Product: Impact of β-Adrenoceptor Blockade on Systemic Inflammation and Coagulation Disturbances in Rats with Acute Traumatic Coagulopathy

Procoagulant and Fibrinolytic Activity after Polytrauma in Rat

Upregulation of canonical transient receptor potential channel in the pulmonary arterial smooth muscle of a chronic thromboembolic pulmonary hypertension rat model

Guided longer pulses from a diagnostic ultrasound and intraclot microbubble enhanced catheter-directed thrombolysis in vivo.

Experimental Evaluation of a New Tissue Factor-Based Topical Hemostat (TT-173) for Treatment of Hepatic Bleeding