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Convenient And Easy Use Rapid Test Reader Influenza A Medical Product With High Accuracy

Brand Name:	AllTest
Model Number:	IFLA-R502
MOQ:	N/A
Price:	Negotiation
Payment Terms:	Ex works
Supply Ability:	10 M tests/month

Detail Information

Product Description

Detail Information

Place of Origin:

China

Certification:

CE, ISO13485

Format:

Cassette

Specimen:

Urine

Kit Size:

25 T/Kit

Cut-Off:

40ng/ml 50ng/ml*

Color:

Blue

Certificate:

Packaging Details:

20cassette/box

Supply Ability:

10 M tests/month

Highlight:

rapid diagnostic test kits

One Step Rapid Test

Product Description

Application:

The Influenza A Rapid Test is an in vitro diagnostic test for the qualitative detection of influenza type A nucleoprotein antigens in nasopharyngeal swab and nasal aspirate samples, using the rapid immunochromatographic method. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It will provide information for clinical doctors to prescribe correct medications. Negative results should be confirmed by other methods, such as cell culture.

Description:

The Influenza A Rapid Test is an immunochromatographic membrane assay that uses highly sensitive monoclonal antibodies to detect influenza type A nucleoprotein antigens in nasopharyngeal swab and nasal aspirate samples.

The test strip is composed of the following parts: namely sample pad, reagent pad, reaction membrane, and absorbing pad. The reagent pad contains the colloidal-gold conjugated with the monoclonal antibodies against Influenza virus A; the reaction membrane contains the secondary antibodies for virus A, and the polyclonal antibodies against the mouse globulin, which are pre-immobilized on the membrane. The whole strip is fixed inside a plastic plate.

When the sample is added into the sample window, conjugates dried in the reagent pad are solubilized and migrate along with the sample. If influenza A is present in the sample, a complex formed between the anti-influenza A conjugate and the virus will be captured by the specific anti-influenza A monoclonal coated on the Test Region (T). Results appear at 15 minutes in the form of a red line that develops on the membrane.

To serve as a procedural control, a red line will always appear in the control region(C) indicating that proper volume of sample has been added and membrane wicking has occurred.

How to use?

Allow the test cassette, specimen, extraction buffer to equilibrate to room temperature (15-30°C) prior to test.

1.Exact QR Code from the QR code card for specific information of the test. Use only QR code card provided inside the test kits.

2.Remove the test cassette from the sealed foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed immediately after opening the foil pouch.

3.Place the Extraction Tube in the workstation. Hold the extraction reagent bottle upside down vertically. Squeeze the bottle and let the solution drop into the extraction tube freely without touching the edge of the tube. Add 10 drops of solution (Approx. 400μl) to the Extraction Tube. See illustration 1.

4.Place the swab specimen in the Extraction Tube. Rotate the swab for approximately 10 seconds while pressing the head against the inside of the tube to release the antigen in the swab. See illustration 2.

5.Remove the swab while squeezing the swab head against the inside of the Extraction Tube as you remove it to expel as much liquid as possible from the swab. Discard the swab in accordance with your biohazard waste disposal protocol. See illustration 3.

6.Fit the dropper tip on top of the extraction tube. Place the test cassette on a clean and level surface. See illustration 4

7.Add 3 drops of the solution (approx.120μl) to the sample well and then start the timer.

8.Wait for the colored line(s) to appear. The result should be read with AllTest™ LF Reader at 15 minutes.

9.For Alltest™ LF Reader installation, start up and complete instructions refer to Alltest™ LF Reader User Manual. Operator must consult the Alltest™ LF Reader User Manual prior to use and become familiar with the processes and quality control procedures.

10.Do not interpret test results visually.

Note: For the Reader installation, start up and complete instructions refer to the Reader User Manual. Operator must consult the Reader User Manual prior to use and become familiar with the processes and quality control procedures.

Note: It is suggested not to use the buffer beyond 30 days after opening the vial.

Convenient And Easy Use Rapid Test Reader Influenza A Medical Product With High Accuracy 0

INTERPRETATION OF RESULTS

Results read by Alltest LF reader

The result of positive or negative for Influenza A is determined by the Alltest LF reader.

Result could be exported to excel.

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products details

Convenient And Easy Use Rapid Test Reader Influenza A Medical Product With High Accuracy

Convenient And Easy Use Rapid Test Reader Influenza A Medical Product With High Accuracy

rapid diagnostic test kits

One Step Rapid Test