PROTIA™ Allergy-Q
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+82-2-323-8343 /
protia@proteometech.com
Intended use
Assay kit for quantitative determination of specific IgE antibodies against individual allergens in human serum using immunoblotting technique
In vitro diagnostic use (IVD)
Product Image & Description
- The World’s highest allergen count in a strip panel.
– Over 60 allergens per strip, total 134 allergens. - Compact configuration
– Two columns of allergen loaded in a single strip to save time and cost.
– Increases the number of analyzed allergen per operation by twice. - Small blood volume for testing
– Requires only 50 μL of serum or plasma for over 60 allergens test (useful for pediatric purpose) - On-strip calibration
– Quantitative analysis by the use of multiple standard lines in a single strip - Clear and informative report format
Easy, Fast and Economic Procedures → Consistent and Reliable Results
The type of panel
Action mechanism and Platform technology
Platform technology : PLA Technology
Novel technique putting more marker lines in a smaller chip by parallel line array
→ More efficient and economic assay
Applicable to many kinds of biochip assay using line-type blotting
Award ＆ Certificate
ISO 13485
Korea Technology Awards(2016)
Jang Young-Shil Award(2015)
ImmuneCheck™ IgG
Intended use
Real-time monitoring of human IgG content based on immunochromatography technique
In vitro diagnostic use
The Product Image & The advantages of ImmuneCheck IgG
ImmuneCheck IgG / 20 tests
ImmuneCheck IgG-F / 1 test
- World’s first direct whole blood test kit for total IgG concentration measurement.
- Results in 20 minutes without any instrument.
- Uses 5 ul of blood sample.
Test procedure
Action mechanism and Platform technology
Novel technique loading two control lines in a strip using different action mechanisms (sandwich methods and competition method)
Correct quantitation, regardless of hooking effect
Applicable to many kinds of rapid test, especially those requiring wide rang of test (up to 106 range)
NET (New Excellent Technology) of 2013 certified by Korean Government
Award & Certificate
Certificate(2015)
ISO13485
Pregnancy Test
TriCheck
Intended use
“TriCheck-C”, an in vitro diagnostic kit, uses immunochromatography method for the qualitative test of hCG
(human Chorionic Gonadotropin) in human urine samples for the pregnancy diagnosis.
The advantages of TriCheck
TriCheck(Midstream type)
TriCheck- C (Cassette type)
Free from the risk of false-negative by the Hook effect of hCG and hCGβcf.
- Quick urine test that can be done in 3~5 minutes for early pregnancy diagnosis by detection of
hCG concentration above 25 mIU/mL - Can be used throughout all periods of pregnancy
- Applicable also for those with irregular menstrual cycle.
- Reliable pregnancy test that overcomes the false negative misinterpretation
due to high concentration of hCG & hCGβcf - Pregnancy test with enhanced precision with an additional test line.
The characteristics of TriCheck
Additional test line (test line 2) only available in Tricheck
Allows determination even in excessively high hGC level.
Action mechanism and Platform technology
Q-Rapid Test AD technology
Rapid immuno-assay kit that enables quantitative measurement in wider range
Principle: Two different assay (Sandwich method, Competition method) on a single test
(First concept in the world, Patent applied)
Certificate
Certificate
New Excellent Technology from Ministry of Health
and Welfare, Republic of Korea, 2015
(Certificate No. 00111)
KFDA
Approval from MFDS(former, KFDA), 2016
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Innovative Technology
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