Multiplex Assay Kit for Fibrinogen Degradation Product (FDP) ,etc. by FLIA (Flow Luminescence Immunoassay) Oryctolagus cuniculus (Rabbit) Multiplex ELISA

FnDP; Fibrin Split Products; Fibrin Degradation Product

(Note: Up to 8-plex in one testing reaction)

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  • Multiplex Assay Kit for Fibrinogen Degradation Product (FDP) ,etc. by FLIA (Flow Luminescence Immunoassay) Packages (Simulation)
  • Multiplex Assay Kit for Fibrinogen Degradation Product (FDP) ,etc. by FLIA (Flow Luminescence Immunoassay) Packages (Simulation)
  • Multiplex Assay Kit for Fibrinogen Degradation Product (FDP) ,etc. by FLIA (Flow Luminescence Immunoassay) Results demonstration
  • LMA530Rb.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Recovery

Matrices listed below were spiked with certain level of recombinant Fibrinogen Degradation Product (FDP) and the recovery rates were calculated by comparing the measured value to the expected amount of Fibrinogen Degradation Product (FDP) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 82-99 88
EDTA plasma(n=5) 97-105 101
heparin plasma(n=5) 85-99 95

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fibrinogen Degradation Product (FDP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Fibrinogen Degradation Product (FDP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Fibrinogen Degradation Product (FDP) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
serum(n=5) 80-98% 92-101% 78-104% 84-98%
EDTA plasma(n=5) 88-95% 93-101% 96-104% 80-90%
heparin plasma(n=5) 86-101% 83-92% 84-101% 90-103%

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.

Reagents and materials provided

Reagents Quantity Reagents Quantity
96-well plate 1 Plate sealer for 96 wells 4
Pre-Mixed Standard 2 Standard Diluent 1×20mL
Pre-Mixed Magnetic beads (22#:FDP) 1 Analysis buffer 1×20mL
Pre-Mixed Detection Reagent A 1×120μL Assay Diluent A 1×12mL
Detection Reagent B (PE-SA) 1×120μL Assay Diluent B 1×12mL
Sheath Fluid 1×10mL Wash Buffer (30 × concentrate) 1×20mL
Instruction manual 1

Assay procedure summary

1. Add 200μL analysis buffer solution to each well of the plate for pre-wetting;
2. Preparation of standards, reagents and samples before the experiment;
3. Add 50μL standard or sample to each well, add 50μL prepared Detection Reagent A, add 10μL magnetic beads, and incubate 90 minutes protect from light at 25°C on shaker;
4. Remove liquid on magnetic frame, add 100μL prepared Detection Reagent B, and incubate 30 minutes protect from light at 25°C on shaker;
5. Wash plate once on magnetic frame;
6. Add 100μL sheath fluid, swirl for 10 minutes, read on the machine.

Multiplex Assay Kit for Fibrinogen Degradation Product (FDP) ,etc. by FLIA (Flow Luminescence Immunoassay)

Test principle

Anti-Fibrinogen Degradation Product (FDP) antibody was coated on the surface of magnetic beads. A competitive inhibition reaction is launched between biotin labeled Fibrinogen Degradation Product (FDP) and unlabeled Fibrinogen Degradation Product (FDP) (Standards or samples) with the pre-coated antibody specific to Fibrinogen Degradation Product (FDP). PE-labeled avidin was added. The amount of bound PE conjugate is reverse proportional to the concentration of Fibrinogen Degradation Product (FDP) in the sample, the intensity of MFI developed is reverse proportional to the concentration of Fibrinogen Degradation Product (FDP) in the sample.

Giveaways

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Citations

  • The role of the E2F1 transcription factor in the innate immune response to systemic LPSPhysiology: Source
  • Thrombomodulin alleviates murine GVHD in association with an increase in the proportion of regulatory T cells in the spleenPubmed:25243628
  • The efficacy of recombinant human soluble thrombomodulin for the treatment of shiga toxin associated hemolytic uremic syndrome model micePubmed:25694534
  • Inhibition of Plasmin Protects Against Colitis in Mice by Suppressing Matrix Metalloproteinase 9–Mediated Cytokine Release From Myeloid CellsSciencedirect:S0016508514014851
  • Inhibition of Plasmin Protects Against Colitis in Mice byPubMed: 25490065
  • Cytoprotective and pro-angiogenic functions of thrombomodulin are preserved in the C loop of the fifth epidermal growth factor-like domainPubmed:29903766
  • Temporary inhibition of the plasminogen activator inhibits periosteal chondrogenesis and promotes periosteal osteogenesis during appendicular bone fracture …10.1016:j.bone.2018.04.016
  • Nebulized anti-coagulants as a therapy for acute lung injury and acute respiratory distress syndromePubmed: 29202212
  • Co-administration of iloprost and eptifibatide in septic shock (CO-ILEPSS)—a randomised, controlled, double-blind investigator-initiated trial investigating …Pubmed: 31488213
  • Effects of nebulized antithrombin and heparin on inflammatory and coagulation alterations in an acute lung injury model in ratsPubmed: 31755229

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