ELISA Kit for Retinol (Ret) Pan-species (General) Competition ELISA

VA; Vitamin A; Aquasola

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  • ELISA Kit for Retinol (Ret) Packages (Simulation)
  • ELISA Kit for Retinol (Ret) Packages (Simulation)
  • ELISA Kit for Retinol (Ret) Results demonstration
  • CED051Ge.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Recovery

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

Matrix Recovery range (%) Average(%)
serum(n=5) 80-101 86
EDTA plasma(n=5) 87-101 95
heparin plasma(n=5) 92-105 96

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Retinol (Ret) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Retinol (Ret) 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 Retinol (Ret) 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) 89-96% 97-105% 85-104% 85-104%
EDTA plasma(n=5) 91-105% 81-98% 94-105% 78-101%
heparin plasma(n=5) 78-101% 81-88% 98-105% 81-102%

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
TMB Substrate 1×9mL Stop Solution 1×6mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1

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.

ELISA Kit for Retinol (Ret)

Test principle

This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Retinol (Ret) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Retinol (Ret) and unlabeled Retinol (Ret) (Standards or samples) with the pre-coated antibody specific to Retinol (Ret). 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 Retinol (Ret) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Retinol (Ret) in the sample.

Citations

  • Effects of Vitamin A Overdose on the Immune system in ratsJpmbs: Source
  • Salivary 1, 5-Anhydroglucitol and Vitamin Levels in Relation to Caries Risk in Children
  • Oxidative stress indicators in Chinese women with PCOS and correlation with features of metabolic syndrome and dependency on lipid patternsPubmed: 31549221
  • Prooxidant effect of α-tocopherol in pancreatic tumors.
  • Vitamin A, C, D, E and B12 Levels in Leprosy: A Case Control Study
  • Protocol: Prevalence of specific micronutrient deficiencies in urban school going children of India aged between 6 and 16 years: study protocol for a …Pubmed:34907037
  • Prevalence of specific micronutrient deficiencies in urban school going children and adolescence of India: A multicenter cross-sectional studyPubmed:35544476
  • Retinol Depletion in COVID-19Pubmed:35664529

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