Mini Samples ELISA Kit for Estrone (E1) Pan-species (General) Mini ELISA

Oestrone

Add to Cart Distributors
Overview
Properties
Share your citation Upload your experimental result Review Leave a message
Loading...

Share a new citation as an author

Upload your experimental result

Review

Please attach serial No. on instruction manual

Contact us

Please fill in the blank.

Name*
Organization
Address
E-mail address*
Telephone
Inquiry*
Verification code* CheckCode
  • Mini Samples ELISA Kit for Estrone (E1) Packages (Simulation)
  • Mini Samples ELISA Kit for Estrone (E1) Packages (Simulation)
  • Mini Samples ELISA Kit for Estrone (E1) Results demonstration
  • MEB003Ge.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Recovery

Matrices listed below were spiked with certain level of Mini Samples Estrone (E1) and the recovery rates were calculated by comparing the measured value to the expected amount of Mini Samples Estrone (E1) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 91-101 94
EDTA plasma(n=5) 82-103 87
heparin plasma(n=5) 82-102 86

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Estrone (E1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Estrone (E1) 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 Mini Samples Estrone (E1) 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) 89-101% 80-93% 83-95% 92-99%
EDTA plasma(n=5) 97-105% 95-102% 90-97% 87-99%
heparin plasma(n=5) 92-104% 94-102% 98-105% 93-101%

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 Assay Diluent A 1×6mL
Detection Reagent B 1×60µL Assay Diluent B 1×6mL
Reagent Diluent 1×300µL Stop Solution 1×3mL
TMB Substrate 1×9mL Instruction manual 1
Wash Buffer (30 × concentrate) 1×10mL

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 25µL standard or sample to each well.
    And then add 25μL prepared Detection Reagent A immediately.
    Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 50µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 50µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 25µL Stop Solution. Read at 450 nm immediately.

Mini Samples ELISA Kit for Estrone (E1)

Test principle

This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Mini Samples Estrone (E1) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Mini Samples Estrone (E1) and unlabeled Mini Samples Estrone (E1) (Standards or samples) with the pre-coated antibody specific to Mini Samples Estrone (E1). 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 Mini Samples Estrone (E1) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Mini Samples Estrone (E1) in the sample.

Citations

  • Association between Polycystic Ovary Syndrome and Cavia (Guinea pig )t MicrobiotaPubmed:27093642
  • Pollution by endocrine disrupting estrogens in aquatic ecosystems in Morogoro urban and peri-urban areas in Tanzania150659
  • Pollution by endocrine disrupting estrogens in aquatic ecosystems in Morogoro urban and peri-urban areas in Tanzania10.5897/AJEST2016.2234
  • Phosphorescent palladium-tetrabenzoporphyrin indicators for immunosensing of small molecules with a novel optical device33379126

Recommend products