Chagas lgG/IgM Rapid Test

Short Description:

Used For: for the qualitative detection of IgG and IgM antibodies to Trypanosoma cruzi in human whole blood, serum or plasma specimen. 

Specimen:human whole blood, serum or plasma specimen. 

Certification:CE

MOQ:1000

Delivery time:2-5 days after Get payment

Packing:20 tests kits/Packing box

Shelf Life:24 Months

Payment:T/T, Western Union, Paypal

Assay Time: 10-15 Minutes


Product Detail

Product Tags

INTENDED USE

The Chagas IgG/IgM Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Trypanosoma cruzi in human whole blood, serum or plasma specimen. .

INTRODUCTION

Chagas disease is an insect-borne, zoonotic infection by the protozoan T. cruzi, which causes a systemic infection of humans with acute manifestations and long term sequelae. It is estimated that 16-18 million individuals are infected worldwide, and roughly 50,000 people die each year from chronic Chagas disease (World Health Organization). Buffy coat examination and xenodiagnosis used to be the most commonly methods in the diagnosis of acute T. cruzi infection. However, both methods are either time consuming or lack of sensitivity. Recently, serological test becomes the mainstay in the diagnosis of Chagas’s disease. In particularly, recombinant antigen based tests eliminate false-positive reactions which are commonly seen in the native antigen tests.

The Chagas IgG/IgM Rapid Test is a rapid test that utilizes a combination of Chagas antigen coated colored particles for the detection of IgG and IgM to  T. cruzi antibodies in human whole blood, serum, or plasma.

PROCEDURE

Allow the test device, specimen, buffer, and/or controls to reach room temperature (1530°C) prior to testing.

  1. Bring the pouch to room temperature before opening. Remove the test device from the sealed pouch and use it as soon as possible.
  2. Place the test device on a clean and level surface.

For Serum or Plasma Specimens

Hold the dropper vertically, draw the specimen up to the Fill Line (approximately 10 uL), and transfer the specimen to the specimen well (S) of the test device, then add 2 drops of buffer (approximately 80 mL) and start the timer. See illustration below. Avoid trapping air bubbles in the specimen well (S).

For Whole Blood (Venipuncture/Fingerstick) Specimens:

To use a dropper: Hold the dropper vertically, draw the specimen 0.5-1 cm above the Fill Line, and transfer 2 drops of whole blood (approximately 20 µL) to the specimen well (S) of the test device, then add 2 drops of buffer (approximately 80 uL) and start the timer. See illustration below.

To use a micropipette: Pipette and dispense 20 µL of whole blood to the specimen well (S) of the test device, then add 2 drops of buffer (approximately 80 µL) and start the timer.

  1. Wait for the colored line(s) to appear. Read results at 10 minutes.Do not interpret the result after 20 minutes.

INTERPRETATION OF RESULTS

 

IgG Positive:* The colored line in the control line region (C) appears, and a colored line appears in test line region G The result is positive for Chagas  specific-IgG and is probably indicative of secondary Chagas infection.

 

IgM Positive:* The colored line in the control line region (C) appears, and a colored line appears in test line region M. The result is positive for Chagas  specific-IgM antibodies and is indicative of primary Chagas infection.

 

IgG and IgM Positive:* The colored line in the control line region (C) appears, and two colored lines should appear in test line regions G and M. The color intensities of the lines do not have to match. The result is positive for IgG & IgM antibodies and is indicative of secondary Chagas infection.

*NOTE: The intensity of the color in the test line region(s) (G and/or M) will vary depending on the concentration of Chagas antibodies in the specimen. Therefore, any shade of color in the test line region(s) (G and/or M) should be considered positive.

 

Negative: The colored line in the control line region (C) appears. No line appears in test line regions G or M.

 

INVALID: No Control line (C) appears. Insufficient buffer volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the procedure with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.






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