Shanghai Eugene Biotech Co.,Ltd

Shanghai Eugene Biotech Co.,Ltd

Shanghai,China

Shanghai Eugene Biotech Co.,Ltd

Shanghai,China

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Shanghai Eugene Biotech Co.,Ltd
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Shanghai Eugene Biotech Co.,Ltd

Shanghai,China

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IgG Antibody to Toxoplasma Gondii Rapid Test

FOB Price : Get a Price/Quote

Min.Order : 1 Set(s)

Certification : CFDA,GMP,ISO13485,CE,FDA

Brand Name : Eugene

Payment Terms : L/C,T/T,WesternUnion

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product information

  • brand name : Eugene

  • certification :

  • fob price :

  • min.order : 1 Set(s)

  • warranty :

  • payment terms : L/C,T/T,WesternUnion

  • Packaing :

  • Specification :

  • Trademark : Eugene

  • Production Capacity :

  • place of origin : China

  • Manag Certifica : CFDA,GMP,ISO13485,CE,FDA

product description

Model: Colloidal Gold Immunoassay Technologies
Certification: ISO13485
Dimension:63cm*41cm*29cm
Packaging Details: Eugene color pouch and inner box, fully packed in export cartons
Brand Name: Eugene
Place of Origin: Shanghai
Warranty: 2 years
Color: white
Size: strip/cassette/midstream
Finish: 7-15Days
Customer's Logo: Eugene
MOQ: 500pcs
Processing Time: 5-10 minutes

Usage: The EUGENE® Tox IgG Serum/Plasma Rapid Test is intended to be used as a screening test and as an aid in the diagnosis of infection with T. gondii.  It is a lateral flow immunoassay for the qualitative detection of IgG antibody to Toxoplasma Gondii (T. gondii) in human serum or plasma. Any reactive specimen with this test must be confirmed with alternative testing method(s) and clinical findings.
Quality: sensitivity:91.60% ; accuracy:98.50%
Packaing: 25T/kit

SUMMARY
T. gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism.
A variety of serological tests for antibodies to T. gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are: the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as the EUGENE® Toxo IgG Serum/Plasma Rapid Test has been introduced to the clinic for the instant detection of T. gondii infection.
ASSAY PROCEDURE
Allow test device, buffer, specimen, and/or controls to equilibrate to room temperature (15-30°C) prior to testing.   
1. Remove the test device from the foil pouch and use it as soon as possible. Do not open the foil pouch without preparation. Best results will be obtained if the assay is performed within one hour.
2. Place the test device on a clean and level surface. Be sure to label the device with specimen’s ID number.
3. Hold the dropper vertically and transfer 2 drops (80μl) of serum or plasma to the specimen well (S) of the test device and start the timer.
4. Wait for the red line(s) to appear. The result should be read at 15-20 minutes. After 30 minutes, the result is ineffective.

 
IgG Antibody to Toxoplasma Gondii Rapid Test
share :

product information

product description

Model: Colloidal Gold Immunoassay Technologies
Certification: ISO13485
Dimension:63cm*41cm*29cm
Packaging Details: Eugene color pouch and inner box, fully packed in export cartons
Brand Name: Eugene
Place of Origin: Shanghai
Warranty: 2 years
Color: white
Size: strip/cassette/midstream
Finish: 7-15Days
Customer's Logo: Eugene
MOQ: 500pcs
Processing Time: 5-10 minutes

Usage: The EUGENE® Tox IgG Serum/Plasma Rapid Test is intended to be used as a screening test and as an aid in the diagnosis of infection with T. gondii.  It is a lateral flow immunoassay for the qualitative detection of IgG antibody to Toxoplasma Gondii (T. gondii) in human serum or plasma. Any reactive specimen with this test must be confirmed with alternative testing method(s) and clinical findings.
Quality: sensitivity:91.60% ; accuracy:98.50%
Packaing: 25T/kit

SUMMARY
T. gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism.
A variety of serological tests for antibodies to T. gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are: the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as the EUGENE® Toxo IgG Serum/Plasma Rapid Test has been introduced to the clinic for the instant detection of T. gondii infection.
ASSAY PROCEDURE
Allow test device, buffer, specimen, and/or controls to equilibrate to room temperature (15-30°C) prior to testing.   
1. Remove the test device from the foil pouch and use it as soon as possible. Do not open the foil pouch without preparation. Best results will be obtained if the assay is performed within one hour.
2. Place the test device on a clean and level surface. Be sure to label the device with specimen’s ID number.
3. Hold the dropper vertically and transfer 2 drops (80μl) of serum or plasma to the specimen well (S) of the test device and start the timer.
4. Wait for the red line(s) to appear. The result should be read at 15-20 minutes. After 30 minutes, the result is ineffective.

 

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