CLIA Kit for Adiponectin (ADP) Mus musculus (Mouse) Sandwich CLIA

GBP28; ApM1; AdipoQ; Acrp30; ACDC; APM1; C1Q And Collagen Domain Containing; Adipocyte Complement-Related Protein Of 30 KDa; Adipose Most Abundant Gene Transcript 1

  • Product No.SCA605Mu
  • Organism SpeciesMus musculus (Mouse) Same name, Different species.
  • Sample TypeSerum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
  • Test MethodDouble-antibody Sandwich
  • Assay Length2h, 40min
  • Detection Range5.49-4,000pg/mL
  • SensitivityThe minimum detectable dose of this kit is typically less than 2.41pg/mL.
  • Specificity This assay has high sensitivity and excellent specificity for detection of Adiponectin (ADP).No significant cross-reactivity or interference between Adiponectin (ADP) and analogues was observed.
  • ApplicationsChemiluminescent immunoassay for Antigen Detection.
  • DownloadInstruction Manual
  • UOM 48T96T 96T*5 96T*10 96T*100 Out of stock
  • FOB US$ 605.00 US$ 864.00 US$ 3,888.00 US$ 7,344.00 US$ 60,480.00
  • Quantity
  • Add to Cart Distributors
  • CLIA Kit for Adiponectin (ADP) Packages (Simulation)
  • CLIA Kit for Adiponectin (ADP) Packages (Simulation)
  • CLIA Kit for Adiponectin (ADP) Results demonstration
  • SCA605Mu.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Recovery

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

Matrix Recovery range (%) Average(%)
serum(n=5) 80-96 92
EDTA plasma(n=5) 80-92 87
heparin plasma(n=5) 87-95 91

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Adiponectin (ADP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Adiponectin (ADP) 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 Adiponectin (ADP) 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) 95-104% 78-96% 81-105% 92-101%
EDTA plasma(n=5) 86-101% 84-99% 85-95% 97-104%
heparin plasma(n=5) 92-102% 78-89% 92-101% 97-104%

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
Pre-coated, ready to use 96-well strip plate 1 Plate sealer for 96 wells 4
Standard 2 Standard Diluent 1×20mL
Detection Reagent A 1×120µL Assay Diluent A 1×12mL
Detection Reagent B 1×120µL Assay Diluent B 1×12mL
Substrate A 1×10mL Substrate B 1×2mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 100µL Substrate Solution. Incubate 10 minutes at 37°C;
8. Read RLU value immediately.

CLIA Kit for Adiponectin (ADP)

Test principle

The microplate provided in this kit has been pre-coated with an antibody specific to Adiponectin (ADP). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Adiponectin (ADP). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Adiponectin (ADP) level in the sample or standard.;

Reference

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