STANDARD Q

COVID-19 IgM/IgG Duo Test

Q-NCOV-01D

Expanded diagnostic coverage from acute to convalescent phase of COVID-19

Mean Titer
Magnitude of response

The outbreak of coronavirus disease Virus �ter

pneumonitis
2019(COVID-19) was first reported from
IgM
**IgM 1:1280
Wuhan, China in December 2019. Early IgG
1:640
diagnosis and appropriate treatment are
1:320
essential to effectively control the 1:160

large-scale transmission of COVID-19. *Virus �ter *pneumoni�s **IgG 1:80

STANDARD Q COVID-19 IgM/ IgG Duo 1:40

Test is suitable for patients who show Incuba�on 1:20

period
negative PCR result with mild pneumoniae 1:10
0 1 2 3 4 5 6 7 8 9 10 11 12 ~ Days post infec�on
symptoms or have persisted pneumoniae
Infec�on Onset of Symptoms
symptoms for more than 10 days. An�body test is appropriate for asymptoma�c or convalescent pa�ents.
PCR test is appropriate for
acute phase of illness IgM Test
IgG test
PCR
Reference : Cellular immune responses to severe acute respiratory syndrome coronavirus infec�on in senescent BALB/c Mice:CD4+ T cells are important in control of SARD-CoV infec�on. Jun Chen.
Chronological evolu�on of IgM, IgA, IgG and neutraliza�on an�bodies a�er infec�on with SARD-Associated coronavirus. P.R Hsueh.
Mechanisms of Host defense following severe acute respiratory syndrome-coronavirus pulmonary infec�on of mice.
SARS immunity and vaccina�on. Minsheng Zhu.

* Virus titer and pneumonitis : Time course of host responses to primary SARS-CoV infection in mice.
** Antibody titer : Dynamic changes of IgG and IgM against SARS-CoV in patients.
*** The antibody titer may vary depending on the patient's immune status.

STANDARD Q COVID-19 IgM/IgG Duo Test

The STANDARD Q COVID-19 IgM/IgG Duo Test kit is a rapid immunochromatography test designed for the qualitative
presumptive detection of specific IgM and IgG to 2019 novel coronavirus (nCoV) in humoral fluid.

Benefits
· Rapid testing for nCoV antibodies within 10 minutes
· Just 10ul of specimen : Whole blood, serum , plasma
· Suitable for Point of Care Testing. No need for extra equipment.

Specification
Information Detail
Time to result 10 minutes
Storage and operating conditions 2-40℃/36-104℉
Shelf life 24 months
Sample type Whole blood/Serum/plasma
Specificity 95%(95/100)
 STANDARD Q COVID-19 IgM/IgG Duo Test

Simple Test Procedure

The test procedure for COVID-19 IgG
The test procedures for both COVID-19 IgM and IgG are the same.

1 Collecting of Sample 2 Adding of Sample 3 Dropping of Assay diluent 4 Reading Time

Using an STANDARD Ezi
Tube+, collect the 10μl of
serum/plasma/whole blood
to the black line of the
STANDARD Ezi Tube+.
Add the collected serum/plas-
ma/whole blood to the sample
well of the test device.
Discard the Ezi tube+into
the disposal bag after use.
Add 3 drops (90μl) of assay
diluent into the assay diluent
well of the test device.
Assay diluent
Read test result at 10~15
minutes.
Discard the test device into
the disposal bag after use.

10µl
Read

10µl 3 drops After 10 mins

Do not read
After 15 mins

10 mins
Do not read test results
after 15 minutes. It may
give false results.
CAUTION

Interpretation
Positive Negative Invaild

COVID-19 IgM COVID-19 IgG COVID-19 IgM and IgG

Positive Positive Positive

1. A colored band will appear in the top section of the result window to show that the test is working properly. This band is control line (C).
2. A colored band will appear in the lower section of the result window. These bands are test line of IgM/IgG (M, G).
3. Even if the control line is faint, or the test line isn't uniform, the test should be considered to be performed properly and the test result should be
interpreted as a positive result.
* Positive results should be considered in conjunction with the clinical history and other data available to the physician.
* STANDARD Q COVID-19 IgM/IgG Duo Test may cross-react with SARS antibodies.

Ordering Infomation

Product Cat. No. Storage temperature Shelf life Pack size

STANDARD Q COVID-19 IgM/IgG Duo 09COV10A 2-40℃/36-104℉ 24 months 10T/kit

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