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  • bovine serum albumin elisa 1

BlueGene Biotech Human Protein Induced by Vitamine k absence or antagonist II ELISA kit (E01P1008)

E01P1008 Human Protein Induced by Vitamine k absence or antagonist II ELISA kit

The Human Protein Induced by Vitamine k absence or antagonist II ELISA kit can be used to identify samples from the human species. Protein Induced by Vitamine k absence or antagonist II can also be called PIVKA-II, PIVKA2, DCP, antagonist-II, Des-gamma carboxyprothrombin.

Products

Specifications of Human Protein Induced by Vitamine k absence or antagonist II ELISA kit

Product Information

Cat. No.

E01P1008

Product Name

Human Protein Induced by Vitamine k absence or antagonist II ELISA kit

Species

Human

Product Size

48 Tests / 96 Tests

Concentration

1.0-25 ng/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)

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

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


Quality Control on Human Protein Induced by Vitamine k absence or antagonist II 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 PIVKA-II and analogues was observed.


BlueGene Biotech Product Show

Summary of the Assay Procedure for Human Protein Induced by Vitamine k absence or antagonist II ELISA kit

Summary of the Assay Procedure for Human Protein Induced by Vitamine k absence or antagonist II ELISA kit

Citations of Human Protein Induced by Vitamine k absence or antagonist II ELISA kit

E01P1008 has been referenced in the below publications:

Comparing Prothrombin induced by vitamin K absence-II (PIVKA-II) with the oncofetal proteins Glypican-3, Alpha feto protein and Carcinoembryonic antigen in diagnosing hepatocellular carcinoma among Egyptian patients.

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