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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

제품과-기기-사진-및-이름-1030×258
영문_알러지큐 설명

Easy, Fast and Economic Procedures      Consistent and Reliable Results

The type of panel

96M 패널_영문

64_Inhalant_영문

64_food_영문

64s

atopy_영문

Action mechanism and Platform technology

allergy-panel

Platform technology : PLA Technology

패널 종류

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 : 2016

Korea Technology Awards(2016)

awards2016

Jang Young-Shil Award(2015)

awards2015

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

kitmethod_EN
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

New technology certification from the Ministry of Trade, Industry and Energy

ISO 13485 : 2016

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

트리첵-트리첵-C 사진

트리첵_미드스트림

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

tricheck-test

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

Allows determination even in excessively high hGC level.

Action mechanism and Platform technology

tricheck5

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)

World-class product certificate

tricheck_cert_en

KFDA

제조허가증 class=

Approval from MFDS(former, KFDA), 2016

Intended use

Unlike normal IgE allergy, IgG-mediated allergy can occur a few hours or days after food intake, and symptoms vary, making it difficult to identify the cause.
If you have abnormal symptoms of the gastrointestinal tract such as constipation, stomachache, etc. or various symptoms that can not figure out the cause, you should consider food allergy.
Through PROTIA Food IgG, identify the foods that do not fit, and stay healthy!

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Product image & Description

  • 1 μL of serum volume for testing
  • Compact diagnostic panel
  • On-strip calibration
  • Line blot immunoassay
  • Valuable and informative report format
  • Applicable to Automatic & Semi-Automatic instrument

Information of the panel

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Intended use

 Animal allergy is found to have symptoms of all ages.  The symptoms of allergy vary, such as atopic dermatitis, toe licking, hair loss, etc. furthermore, it is hard to identify allergy symptoms due to secondary bacterial infection. ANITIA Canine IgE, with an only small volume of serum you can identify the cause of the allergy, and provide a safe place for your pet by eliminating the factor that causes allergy.

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Product image & Description

  • 50 μL of serum volume for testing
  • 66 specific IgE test
  • On-strip calibration
  • Line blot immunoassay

Information of the panel

Action mechanism and technology

Platform technology

Parallel line array (PLA) multiplex biochip technology

Increase efficiency of test up to 2 fold by patent technology (KR 1570327)

AniCheck Bovine IgG colostrum

AniCheck

Intended use

Calves are Immune-deficient when they are born.

Feed your calves with appropriate colostrum containing high concentration of IgG to save them.

Product image & Description

Test Procedures

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1.Collect 5ul of colostrum with capillary tube.

2.Put tube, filled with colostrum, into the diluent

3.Shake the bottle to blend colostrum and the diluent

4.Put 4 drops on the sample pad of the cassette.

5.Wait for 10 minutes for the result.

for COVID-19 diagnostic assay

GENEdania

Overview

Protect yourself from silent infection by highly specific GENEdania COVID-19 qRT-PCR

The GENEdania COVID-19 qRT-PCR is an in vitro diagnostic (IVD) one step real-time RT-PCR  kit for the detection of nucleic acid from SARS-CoV-2. It targets the Orf1ab gene and the N gene for SARS-CoV-2 (COVID-19), specifically. The E gene for beta coronavirus and endogenous control gene for kit verification are also included in a single tube. All four genes are amplified simultaneously in one tube and give the accurate results less than 2 hours from purified COVID-19 RNA samples. This kit can be applied to the sample from upper respiratory specimens e.g. nasopharyngeal, oropharyngeal swab and lower respiratory specimens, e.g. sputum, from individuals with signs and symptoms of COVID-19.

Key Features

  • Detects three COVID-19 genes
    : Orf1ab, N and E genes and endogenous control gene
  • Full compliance with the WHO Guidelines
  • Less than 2 hours from RNA to results on most qPCR machines
  • One tube and one step real-time RT-PCR assay Kit
  • UDG (Uracil-DNA Glycosylase) to eliminate the carry-over contamination during the RT-PCR assay

Key Components

Running Program

Analysis of Results

Set on Threshold and Baseline

Result Interpretation

Ct. value for Positive and Negative controls

Analytes

COVID-19 IgG/IgM

KOVIcheck

Overview

Protect yourself from serious infection with highly specific KOVIcheck

COVID-19 (Corona Virus disease 2019) is the respiratory infectious disease caused by SARS-CoV-2 that has not been previously identified in humans. WHO declared this beta-coronavirus as a pandemic disease being regarded as spreading all around the world.

Immunochromatographic assay

for detection of SARS-CoV-2 specific

human Immunoglobulin G and Immunoglobulin M.

table_kovicheck_overview

Key Features

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  • Rapid Test for SARS-CoV-2 antibodies within 15 minutes.
  • Available for whole blood, serum or plasma.
  • 96% of sensitivity, 98-100% of specificity.

Detection of COVID-19 specific IgM antibody indicates a recent exposure to COVID-19, whereas detection of COVID-19 specific IgG antibody indicates a later stage of infection.

So, this combined antibody test could provide information on the stage of COVID-19 infection.

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KIT CONTENTS

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TEST PROCEDURE

Using Capillary whole blood

   Collecting Specimen
Take blood using a lancet, collect 20 µL of blood sample by contacting the tip of the dropper to blood.

kovicheck_procedure_01

   Adding of Specimen
Add the collected whole blood into the specimen well (S) of the test cassette.

kovicheck_procedure_02

  Dropping of buffer
Add 3 drops (about 90 µL) buffer vertically into the buffer well (B) of the test cassette.

kovicheck_procedure_03

Reading Time
Read test result in 10-15 minutes.

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Using of serum/ plasma/ venous whole blood.

   Collect of Specimen
Using micropipette, collect the 10 µL of serum/ plasma/ venous whole blood.

kovicheck_procedure_05

  Adding of Specimen
Add the collected serum, plasma or venous whole blood into the specimen well (S) of the cassette.

kovicheck_procedure_06

    Dropping of buffer
Add 3 drops (about 90 µL) buffer vertically into the buffer well (B) of the test cassette.

kovicheck_procedure_07

    Reading Time
Read test result in 10-15 minutes.

kovicheck_procedure_08

INTERPRETATION OF TEST RESULT

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