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  • bovine serum albumin elisa 1
  • bovine serum albumin elisa 1

BlueGene Biotech Rat Androgen ELISA kit (E02A0019)

E02A0019 Rat Androgen ELISA kit

Rat Androgen ELISA kit is suitable for the detection of samples from Rat species. Androgen can also be called ADG.


Products

Specifications of Rat Androgen ELISA kit

Product Information

Cat. No.

E02A0019

Product Name

Rat Androgen ELISA kit

Species

Rat

Product Size

48 Tests / 96 Tests

Concentration

0.5-10ng/ml

Sensitivity

0.1 ng/mL

Principal

Competitive ELISA

Sample Volume

100 ul

Sample Type

Serum, plasma, cell culture supernatants, body fluid and tissue homogenate

Assay Time

90 minutes

Platform

Microplate Reader

Conjugate

HRP

Detection Method

Colorimetric

Storage

2-8°C



Kit Components

MATERIALS

SPECIFICATION

QUANTITY

MICROTITER PLATE

96 wells

stripwell

ENZYME CONJUGATE

6.0 mL

1 vial

STANDARD A (0.5mL)

0 ng/mL

1 vial

STANDARD B (0.5mL)

0.5 ng/mL

1 vial

STANDARD C (0.5mL)

1.0 ng/mL

1 vial

STANDARD D (0.5mL)

2.5 ng/mL

1 vial

STANDARD E (0.5mL)

5.0 ng/mL

1 vial

STANDARD F (0.5mL)

10 ng/mL

1 vial

SUBSTRATE A

6 mL

1 vial

SUBSTRATE B

6 mL

1 vial

STOP SOLUTION

6 mL

1 vial

WASH SOLUTION (100 x)

10 mL

1 vial

BALANCE SOLUTION

3 mL

1 vial


Principle of the Assay

ADG ELISA kit applies the competitive enzyme immunoassay technique utilizing an anti-ADG antibody and an ADG-HRP conjugate. The assay sample and buffer are incubated together with ADG-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the ADG concentration since ADG from samples and ADG-HRP conjugate compete for the anti-ADG antibody binding site. Since the number of sites is limited, as more sites are occupied by ADG from the sample, fewer sites are left to bind ADG-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ADG concentration in each sample is interpolated from this standard curve.


Quality Control on Rat Androgen ELISA kit

Coefficient of Variance

Intra Variation% <10%

Inter Variation% <12%

Recovery

95-107%

Linearity

Diluent Ratio

Range %

1:2

93-102

1:4

90-106

1:8

90-109

Specificity/Cross-reactivity

No significant cross-reactivity or interference between ADG and analogues was observed.


BlueGene Biotech Product Show

Summary of the Assay Procedure for Rat Androgen ELISA kit

Summary of the Assay Procedure for Rat Androgen ELISA kit

Citations of Rat Androgen ELISA kit

E02A0019 has been referenced in the below publications:

GFW Modified act on Polycystic Ovary Syndrome in ExPerimental and Clinical Efficacy of Phlegm and blood stasis type.

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