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Products > Infectious Disease Test > > NGH Gonorrhea Test Device Cassette NGH-S02D
Product name : NGH Gonorrhea Test Device Cassette NGH-S02D
Item : NGH-S02D
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Details:

Product Name

Specimen

Format

Catalog No.

Sensitivity

Cassette width

Certificate

NGH Gonorrhea Test Device

endocervical

or

urethral

specimens

Cassette 

NGH-S02B

 

3.0mm

 

NGH-S02D

4.0mm

 

Specifications

Rapid NGH Gonorrhea Test

Format: cassette

Model No:NGH-S02D

High Accuracy 

Results in 15minutes

INTRODUCTION

One Step Cassette Style Gonorrhea Test is a rapid direct binding test for the visual detection of gonorrhea
 antigen, in the secretory specimen and urine from urogenital system, as an aid in the diagnosis of
gonococcus infection. It is based on the principle of double sandwich immunoassay for the detection of 
gonorrhea antigen in the secretory specimen or urine.

Monoclonal and polyclonal antibodies are employed to identify gonorrhea specifically. Both sensitivity and 
specificity of the test are higher than those of the present methods, which often involve long hours of culturing 
the collected specimen. Test results are not affected by any medication that is being taken. Results are read
visually without any instrumentation. This test is ideal for screening specimen samples containing at least 
1x105 bacteria per ml.

TEST PROCEDURE

1.When you are ready to begin testing, open the sealed pouch by tearing along the notch

Remove the test kit from the pouch.

2.Using the pipette provided, dispense 3 drops (150uL) of the specimen sample onto the

sample well of the cassette.

3. Wait 10-20 minutes and read results. Do not read results after more than 30 minutes.

INTERPRETATION OF RESULTS 

1. Negative: Only one colored band appears on the control (C) region. No apparent bandon the test (T) region.

2. Positive: In addition to a pink colored control (C) band, a distinct pink colored band will

also appear in the test (T) region.

3. Invalid: A total absence of color in both regions is an indication of procedure error

and / or the test reagent deterioration. Repeat the test with a new kit.


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