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PROTIA Allergy-Q

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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

PROTIA Allergy-Q
  1. The World’s highest allergen count in a strip panel.
    – Over 60 allergens per strip, total 134 allergens.
  2. 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.
  3. Small blood volume for testing
    – Requires only 50 μL of serum or plasma for over 60 allergens test (useful for pediatric purpose)
  4. On-strip calibration
    – Quantitative analysis by the use of multiple standard lines in a single strip
  5. Clear and informative report format

Easy, Fast and Economic Procedures      Consistent and Reliable Results

The type of panel

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panel-en2

panel-en3

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Action mechanism and Platform technology

allergy-panel

Platform technology : PLA Technology

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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)

awards2016

Jang Young-Shil Award(2015)

awards2015

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

immuncheck-20tests

ImmuneCheck IgG / 20 tests

ImmuneCheck-1test

ImmuneCheck IgG-F / 1 test

  1. World’s first direct whole blood test kit for total IgG concentration measurement.
  2. Results in 20 minutes without any instrument.
  3. Uses 5 ul of blood sample.

Test procedure

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Action mechanism and Platform technology

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pad

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)

award2015

ISO13485

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

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tricheck

TriCheck(Midstream type)

tricheck-c   TriCheck- C (Cassette type)

Free from the risk of false-negative by the Hook effect of hCG and hCGβcf.

  1. Quick urine test that can be done in 3~5 minutes for early pregnancy diagnosis by detection of
    hCG concentration above 25 mIU/mL
  2. Can be used throughout all periods of pregnancy
  3. Applicable also for those with irregular menstrual cycle.
  4. Reliable pregnancy test that overcomes the false negative misinterpretation
    due to high concentration of hCG & hCGβcf
  5. Pregnancy test with enhanced precision with an additional test line.

The characteristics of TriCheck

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Additional test line (test line 2) only available in Tricheck

Allows determination even in excessively high hGC level.

Action mechanism and Platform technology

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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

신기술인증서

New Excellent Technology from Ministry of Health
and Welfare, Republic of Korea, 2015
(Certificate No. 00111)

KFDA

제조허가증 class=

Approval from MFDS(former, KFDA), 2016

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