Chlamydia Antigen Rapid Test

Product Details
Customization: Available
Type: Detection Card
Syringe: None
Still deciding? Get samples of US$ 0/box
Request Sample
Manufacturer/Factory, Trading Company
Gold Member Since 2021

Suppliers with verified business licenses

Audited Supplier

Audited by an independent third-party inspection agency

Importers and Exporters
The supplier has import and export rights
High Repeat Buyers Choice
More than 50% of buyers repeatedly choose the supplier
to see all verified strength labels (19)
  • Chlamydia Antigen Rapid Test
  • Chlamydia Antigen Rapid Test
  • Chlamydia Antigen Rapid Test
  • Chlamydia Antigen Rapid Test
  • Chlamydia Antigen Rapid Test
  • Chlamydia Antigen Rapid Test
Find Similar Products

Basic Info.

Model NO.
HCT024G
Breathing Pattern
None
Animal Anesthesia Machine Control Method
None
Assay Time
5-10 Minutes
Delivery Time
3~5days After Get Payment
Payment
T/T, Western Union, Paypal
Customized
Accpet
Transport Package
Carton
Specification
10Tests/Kit
Trademark
PETX
Origin
Hangzhou
HS Code
38220010
Production Capacity
5000000PCS/Year

Product Description


INTENDED USE
The Monkeypox virus IgG Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of IgG antibodies to Monkeypox virus in human whole blood, serum, or plasma as an aid in the diagnosis of Monkeypox infections.

SUMMAR
MATERIALS

Materials Provided
  • Individually packed test devices
  • Disposable pipettes
  • Package insert
  • Buffer
Materials Required but Not provided
  • Centrifuge
  • Micropipette
  • Timer
  • Lancets

TEST 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
Chlamydia Antigen Rapid Test

POSITIVE: Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).

NEGATIVE: Only one colored band appears in the control region (C). No apparent colored band appears in the test region (T).
INVALID: Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.
NOTE:
  1. The intensity of color in the test region (T) may vary depending on the concentration of analytes present in the specimen. Therefore, any shade of color in the test region should be considered positive. Note that this is a qualitative test only, and cannot determine the concentration of analytes in the specimen.
  2. Insufficient specimen volume, incorrect operating procedure or expired tests are the most likely reasons for control band failure.
 

PERFORMANCE CHARACTERIST

Cross-reactivity
Cross-reactivity of the Monkeypox virus IgG Rapid Test was evaluated using serum or plasma specimen which contain antibodies to the pathogens listed below. No false positive or false negative was found with the following.
HCoV-OC43 IgG
HCoV-HKU1 IgG
HCoV-229E IgG
HCoV-NL63 IgG
Influenza A IgM/IgG
Influenza B IgM/IgG
Legionella pneumophila IgM
Chlamydia pneumophila IgM/IgG
Mycoplasma pneumophila IgM
HRSV-IgM
Measles IgG
Mumps IgG
Mycobacterium tuberculosis
COVID19 IgG
Human Adenovirus IgG
Precision
Intra-Assay
Within-run precision has been determined by using 10 replicates of four specimens: a negative, an IgG positive, an IgM positive and an IgG dual positive. The specimens were correctly identified >99% of the time.
Inter-Assay
Between-run precision has been determined by 10 independent assays on the same four specimens: a negative, an IgG positive, an IgM positive and an IgG dual positive. Three different lots of the Monkeypox virus IgG Rapid Test have been tested using these specimens. The specimens were correctly identified >99% of the time. 
 
 

Chlamydia Antigen Rapid TestChlamydia Antigen Rapid Test

Send your message to this supplier

*From:
*To:
*Message:

Enter between 20 to 4,000 characters.

This is not what you are looking for? Post a Sourcing Request Now
Contact Supplier