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BlueGene Biotech Human Chemokine interferon inducible protein 10 ELISA kit (E01C0040)

E01C0040 Human Chemokine interferon inducible protein 10 ELISA kit

The Human Chemokine interferon inducible protein 10 ELISA kit can be used to identify samples from the human species. Chemokine interferon inducible protein 10 can also be called IP 10, CXCL10, C7, IFI10, INP10, IP-10, SCYB10, crg-2, gIP-10, mob-1, C-X-C motif chemokine ligand 10, C-X-C motif chemokine 10.

Products

Specifications of Human Chemokine interferon inducible protein 10 ELISA kit

Product Information

Cat. No.

E01C0040

Product Name

Human Chemokine interferon inducible protein 10 ELISA kit

Species

Human

Product Size

48 Tests / 96 Tests

Concentration

50-1000 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)

50 pg/mL

1 vial

STANDARD C (0.5mL)

100 pg/mL

1 vial

STANDARD D (0.5mL)

250 pg/mL

1 vial

STANDARD E (0.5mL)

500 pg/mL

1 vial

STANDARD F (0.5mL)

1000 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

IP 10 ELISA kit uses an anti-IP 10 antibody and an IP 10-HRP conjugate in a competitive enzyme immunoassay method. IP 10-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-IP 10 antibody binding site between IP 10 from samples and IP 10-HRP conjugate, the intensity of the color is inversely proportional to the concentration of IP 10. Since the number of sites is limited, as more sites are occupied by IP 10 from the sample, fewer sites are left to bind IP 10-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The IP 10 concentration in each sample is interpolated from this standard curve.


Quality Control on Human Chemokine interferon inducible protein 10 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 IP 10 and analogues was observed.


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Summary of the Assay Procedure for Human Chemokine interferon inducible protein 10 ELISA kit

Summary of the Assay Procedure for Human Chemokine interferon inducible protein 10 ELISA kit

Citations of Human Chemokine interferon inducible protein 10 ELISA kit

E01C0040 has been referenced in the below publications:

Expression and clinical significance of macrophage inflammatory protein-1a,interferon gamma inducible protein 10 and angiopoietin-1in primary acute myelogenous leukemia.

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