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  • bovine serum albumin elisa 1

BlueGene Biotech Human Thrombin antithrombin complex ELISA kit (E01T0502)

E01T0502 Human Thrombin antithrombin complex ELISA kit

The Human Thrombin antithrombin complex ELISA kit can be used to identify samples from the human species. Thrombin antithrombin complex can also be called TAT, Thrombin, Antithrombin Complex, TATC.

Products

Specifications of Human Thrombin antithrombin complex ELISA kit

Product Information

Cat. No.

E01T0502

Product Name

Human Thrombin antithrombin complex ELISA kit

Species

Human

Product Size

48 Tests / 96 Tests

Concentration

2.5-50ng/mL

Sensitivity

0.1ng/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 mL

1 vial

STANDARD A (0.5mL)

0 ng/mL

1 vial

STANDARD B (0.5mL)

2.5 ng/mL

1 vial

STANDARD C (0.5mL)

5.0 ng/mL

1 vial

STANDARD D (0.5mL)

10 ng/mL

1 vial

STANDARD E (0.5mL)

25 ng/mL

1 vial

STANDARD F (0.5mL)

50 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

TAT ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for TAT. Standards or samples are then added to the microtiter plate wells and TAT if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of TAT present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for TAT are added to each well to “sandwich” the TAT immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. 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 TAT 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 TAT concentration in each sample is interpolated from this standard curve.


Quality Control on Human Thrombin antithrombin complex 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 TAT and analogues was observed.


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Summary of the Assay Procedure for Human Thrombin antithrombin complex ELISA kit

Summary of the Assay Procedure for Human Thrombin antithrombin complex ELISA kit

Citations of Human Thrombin antithrombin complex ELISA kit

E01T0502 has been referenced in the below publications:

Procoagulant role of neutrophil extracellular traps in patients with gastric cancer.

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