Cortisol ELISA - Cosmo Bio Co.,Ltd.

Antibodies

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Cortisol ELISA

Catalog No.: ENC-ERKS8003
Size: 1KIT
Price: ¥125000
$1667
antigen/source: Cortisol
Description: standard: native
catalog info: 2008 Japanes Assay kit Catalog-p711
Storage: 4C & -20C
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Immunogen: Porcine
Reacts with: Porcine
Sensitive: 0.2 ng / mL
Measurement Range: 5-600ng/mL
Purpose: The Cortisol ELISA test is an immunoassay designed for the quantitative determination of cortisol in serum/plasma. The test is intended for professional use as an aid in the diagnosis and monitoring of physiological/pathological conditions related to serum/plasma cortisol in Swine and related species.
component: Antibody: X
Plate: X
Coating: X
Control: -
Standard: X
Labeling: X
Substrate: X
Others: X
1. Microtiter wells coated with Cortisol specific antibody.
2. Enzyme labeled (HRP), 12mL
3. Cortisol Standards, 1 set ready to use. (Contains 0, 1.0, 2.5, 5.0,10,50, 200 ng/mL), 0.5ml/vial.
4. TMB Color Reagent (One-step ready to use), 12 mL
5. Stop Solution (2N HCl), 6 mL
6. 20x Wash Buffer, 20 mL.
7. Standard/Sample diluent, 20mL
8. Instructions

Other:

 Supplementary 
Sandwich
 Applicable sample 
Serum, Plasma, Urine
[Other]
The Cortisol Quantitative Test is based on a widely used immunoassay technique. A sample (serum/ plasma/urine) containing an unknown amount of cortisol to be assayed (unlabeled antigen) is added to a standard amount of a labeled derivative of the same substance (labeled antigen). The labeled and unlabeled antigens are then allowed to compete for high affinity binding sites on a limited number of antibodies coated on to the plate. After washing away the free antigen, the amount of labeled antigen in the sample is reversibly proportional to the concentration of the unlabeled antigen. The actual concentrations in unknown samples are obtained by means of a standard curve based on known concentrations of unlabeled antigen analyzed in parallel with the unknowns. In this kit an enzyme label is used. The biospecfic reaction takes place during 1 hour incubation. After washing away, substrate solution is added and the enzyme allowed to react for a fixed time before the reaction is terminated. Absorbencies are measured at 450 nm using ELISA plate reader. A standard curve is produced using values from 6 standards from which absorbency values for blank tubes have been subtracted. Results for unknown may be read directly from this standard curve using either manual calculation or by a suitable computer program.


Reference:

•  BONDY PK. The adrenal cortex, in Randy PT, Rosenberg LE., Metabolic control and disease (8 ed) 1980, WB Sanders, Philadelphia, p1427-1499.
•  Lambert A Clinical Endocrinology 1974, Springer-Verlag New York, p299-305
•  Veosei P, BM, Behrman HR 1974 in Methods in Radioimmuno assay p393-411.
4. Spark R 1971, Internal Med. 75 p75-717
•   Wise T, Zanella EL, Lunstra DD, Ford JJ. J Anim Sci 2000 Jun;78(6):1577-1590
•  Mariscal DV, Bergfeld EG, Cupp AS, Kojima FN, Fike KE, Sanchez T, Wehrman ME, Johnson RK, Kittok RJ, Ford JJ, Kinder JE. Anim Reprod Sci 1998 Dec 1;54(1):31-43
•  Perremans S, Randall JM, Rombouts G, Decuypere E, Geers R. J Anim Sci 2001 Apr;79(4):975-981
•  Schonreiter S, Huber H,Lohmuller V, Zanella AJ, Unshelm J, Henke J, Erhardt W.Tierarztl Prax Ausg G Nutztiere 1999 May;27(3):175-179
 
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