General DHEA sulfate，DHEAS ELISA Kit

SKU Code	LBEK-0089G
Species	General
Sensitivity	0.054ng/mL
Detection Range	0.156-10 ng/mL
Size	96 T \| 48 T
Price	POR

General DHEA sulfate，DHEAS ELISA Kit
Method	Competitive
Samples	In serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.
Intended use	This immunoassay kit allows for the in vitro quantitative determination of General Calcitriol concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of DHEA sulfate 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)	110-120%	100-109%	84-94%	103-113%
EDTA plasma(n=5)	110-120%	97-106%	105-117%	83-92%
heparin plasma(n=5)	113-123%	96-107%	89-101%	94-104%

General Annotation

Function:

Dehydroepiandrosterone sulfate or DHEA sulfate is a metabolite of dehydroepiandrosterone (DHEA) produced by the addition of a sulfate group, catalyzed by the sulfotransferase enzymes SULT1A1 and SULT1E1, which also produce estrone sulfate from estrone. DHEA sulfate can also be back-converted to DHEA through the action of steroid sulfatase.

Additional information

sensitivity	0.054ng/mL
detection-range	0.156-10 ng/mL
brand	Link Biotech

The ELISA is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to General DHEAS, During the reaction, General DHEAS in the sample or standard competes with a fixed amount of biotin-labeled General DHEAS for sites on a pre-coated Monoclonal antibody specific to General. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of General DHEAS in the samples is then determined by comparing the O.D. of the samples to the standard curve.