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

BlueGene Biotech Rat Endotoxin ELISA kit (E02E0134)

E02E0134 Rat Endotoxin ELISA kit

The Rat Endotoxin ELISA kit can be used to identify samples from the rat species. Endotoxin can also be called Lipopolysaccharides, LPS, EDT.

Products

Specifications of Rat Endotoxin ELISA kit

Product Information

Cat. No.

E02E0134

Product Name

Rat Endotoxin ELISA kit

Species

Rat

Product Size

48 Tests / 96 Tests

Concentration

100-2500 pg/mL

Sensitivity

1.0 pg/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 pg/mL

1 vial

STANDARD B (0.5mL)

100 pg/mL

1 vial

STANDARD C (0.5mL)

250 pg/mL

1 vial

STANDARD D (0.5mL)

500 pg/mL

1 vial

STANDARD E (0.5mL)

1000 pg/mL

1 vial

STANDARD F (0.5mL)

2500 pg/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

EDT ELISA kit uses an anti-EDT antibody and an EDT-HRP conjugate in a competitive enzyme immunoassay method. EDT-HRP conjugate is incubated with the assay sample and buffer in a pre-coated plate for one hour. The wells are decanted and washed five times when the incubation period is over. The HRP enzyme substrate is then incubated in the wells. The result of the enzyme-substrate reaction is a complex that is blue in hue. The process is finally stopped by adding a stop solution, causing the solution to turn yellow. In a microplate reader, the color intensity is measured spectrophotometrically at 450 nm. Due to competition for the anti-EDT antibody binding site between EDT from samples and EDT-HRP conjugate, the intensity of the color is inversely proportional to the concentration of EDT. Since the number of sites is limited, as more sites are occupied by EDT from the sample, fewer sites are left to bind EDT-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The EDT concentration in each sample is interpolated from this standard curve.


Quality Control on Rat Endotoxin ELISA kit

Coefficient of Variance

Intra Variation% <10%

Inter Variation% <12%

Recovery

95-102%

Linearity

Diluent Ratio

Range %

1:2

93-105

1:4

88-106

1:8

86-108

Specificity/Cross-reactivity

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


BlueGene Biotech Product Show

Summary of the Assay Procedure for Rat Endotoxin ELISA kit

Summary of the Assay Procedure for Rat Endotoxin ELISA kit

Citations of Rat Endotoxin ELISA kit0510_copy20230510

E02E0134 has been referenced in the below publications:

Protective effects and mechanisms of betaine on liver cirrhosis induced  by multiple pathogenic factors in rats.


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