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

BlueGene Biotech Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit (E01F0035)

E01F0035 Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit

The Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit can be used to identify samples from the human species. Fatty Acid Binding Protein 4, Adipocyte can also be called FABP4, A-FABP, AFABP, ALBP, HEL-S-104, aP2, fatty acid binding protein 4, adipocyte Protein 2.

Products

Specifications of Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit

Product Information

Cat. No.

E01F0035

Product Name

Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit

Species

Human

Product Size

48 Tests / 96 Tests

Concentration

1.0-25 ng/ml

Sensitivity

0.1 ng/ml

Principal

Sandwich ELISA

Sample Volume

50 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

10.0 mL

1 vial

STANDARD A (0.5mL)

0 ng/mL

1 vial

STANDARD B (0.5mL)

1.0 ng/mL

1 vial

STANDARD C (0.5mL)

2.5 ng/mL

1 vial

STANDARD D (0.5mL)

5.0 ng/mL

1 vial

STANDARD E (0.5mL)

10 ng/mL

1 vial

STANDARD F (0.5mL)

25 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

FABP4 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for FABP4. Standards or samples are then added to the microtiter plate wells and FABP4 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of FABP4 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for FABP4 are added to each well to “sandwich” the FABP4 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound coFABP4nents. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain FABP4 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The FABP4 concentration in each sample is interpolated from this standard curve.


Quality Control on Human Fatty Acid Binding Protein 4, Adipocyte 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 FABP4 and analogues was observed.


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Summary of the Assay Procedure for Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit

Summary of the Assay Procedure for Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit

Citations of Human Fatty Acid Binding Protein 4, Adipocyte ELISA kit

E01F0035 has been referenced in the below publications:

The clinical study of metabolic disorders and the correlation with Adipocytokines in PCOS women.

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