QuicKey Pro Horse E2 (Estradiol) ELISA Kit

Referentie E-OSEL-HS0001-96T

Formaat : 96T

Merk : Elabscience

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Product Summary

Get more sensitive and precise results with saving at least 1-2h comparing to traditional ELISA Kits. The new developed technology in house will help to accelerate your science research in a more efficient way.

Sensitivity 3.46 pg/mL
Detection Range 7.81-500 pg/mL
Sample Volume 50 μL
Total Assay Time 1 h 30 min
Reacitivity Horse
Specificity This kit recognizes Horse E2 in samples.No significant cross-reactivity or interference between Horse E2 and analogues was observed
Recovery 80%-120%
Sample Type serum, plasma
Detection Method Colorimetric method, ELISA, Competitive
Assay Type Competitive-ELISA
Size 96T / 48T / 24T / 96T*5 / 96T*10
Storage 2-8℃
Expiration Date 6 months
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Horse E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Horse E2 are added to the micro ELISA plate wells. Horse E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Horse E2 in the samples is then determined by comparing the OD of the samples to the standard curve.
Estradiol is the most potent estrogen of a group of endogenous estrogen steroids which includes estrone and estriol. In women estradiol is responsible for growth of the breast and reproductive epithelia, maturation of long bones and development of the secondary sexual characteristics. Estradiol is produced mainly by the ovaries with secondary production by the adrenal glands and conversion of steroid precursors into estrogens in fat tissue.
Research Area Cell Biology , Metabolism
Other Clones

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