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

BlueGene Biotech Rat Adipose Triglyceride Lipase ELISA kit (E02A0893)

E02A0893 Rat Adipose Triglyceride Lipase ELISA kit

The Rat Adipose Triglyceride Lipase ELISA kit can be used to identify samples from the rat species. Adipose Triglyceride Lipase can also be called PNPLA2, 1110001C14Rik, ATGL, PEDF-R, TTS-2.2, TTS2, iPLA2zeta, FP17548, patatin like phospholipase domain containing 2.

Products

Specifications of Rat Adipose Triglyceride Lipase ELISA kit

Product Information

Cat. No.

E02A0893

Product Name

Rat Adipose Triglyceride Lipase ELISA kit

Species

Rat

Product Size

48 Tests / 96 Tests

Concentration

10-250 ng/mL

Sensitivity

1.0 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)

10 ng/mL

1 vial

STANDARD C (0.5mL)

25 ng/mL

1 vial

STANDARD D (0.5mL)

50 ng/mL

1 vial

STANDARD E (0.5mL)

100 ng/mL

1 vial

STANDARD F (0.5mL)

250 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

ATGL ELISA kit uses an anti-ATGL antibody and an ATGL-HRP conjugate in a competitive enzyme immunoassay method. ATGL-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-ATGL antibody binding site between ATGL from samples and ATGL-HRP conjugate, the intensity of the color is inversely proportional to the concentration of ATGL. Since the number of sites is limited, as more sites are occupied by ATGL from the sample, fewer sites are left to bind ATGL-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ATGL concentration in each sample is interpolated from this standard curve.


Quality Control on Rat Adipose Triglyceride Lipase 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 ATGL and analogues was observed.


BlueGene Biotech Product Show

Summary of the Assay Procedure for Rat Adipose Triglyceride Lipase ELISA kit

Summary of the Assay Procedure for Rat Adipose Triglyceride Lipase ELISA kit

Citations of Rat Adipose Triglyceride Lipase ELISA kit

E02A0893 has been referenced in the below publications:

An experimental study on the regulation of ATGL and TNF-a for NAFLD rats by Fenofibrate and Simvastatin.


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