CLIA Kit for Tetraspanin 30Cluster of Differentiation 63 (CD63) Homo sapiens (Human) Sandwich CLIA

TSPAN30; LAMP-3; ME491; MLA1; OMA81H; Melanoma 1 antigen; Granulophysin; Lysosomal-associated membrane protein 3; Ocular melanoma-associated antigen

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  • CLIA Kit for Tetraspanin 30Cluster of Differentiation 63 (CD63) Packages (Simulation)
  • CLIA Kit for Tetraspanin 30Cluster of Differentiation 63 (CD63) Packages (Simulation)
  • CLIA Kit for Tetraspanin 30Cluster of Differentiation 63 (CD63) Results demonstration
  • SCB345Hu.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Tetraspanin 30Cluster of Differentiation 63 (CD63) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Tetraspanin 30Cluster of Differentiation 63 (CD63) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

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 Tetraspanin 30Cluster of Differentiation 63 (CD63)

Test principle

The microplate provided in this kit has been pre-coated with an antibody specific to Tetraspanin 30Cluster of Differentiation 63 (CD63). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Tetraspanin 30Cluster of Differentiation 63 (CD63). 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 Tetraspanin 30Cluster of Differentiation 63 (CD63) level in the sample or standard.;

Citations

  • Upstream Hedgehog signaling components are exported in exosomes of cervical cancer cell linesPubmed: 30265222
  • Evaluating the Platelet Activation Related to the Degradation of Biomaterials by Scheme of Molecular Markers
  • Evaluating Platelet Activation Related to the Degradation of Biomaterials Using Molecular MarkersPubmed: 32812629
  • Feasibility study of use of rabbit blood to evaluate platelet activation by medical devicesPubmed: 31838449
  • Biomechanical Properties of Blood Plasma Extracellular Vesicles Revealed by Atomic Force Microscopy33374530

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