Miscellaneous diseases diagnosis

PG-I/PG-II Quantitative Test Kit

Time-Resolved Fluorescent Immunochromagraphic Assay

【General Information】

1.Method: Time-resolved Fluorescent Immunochromatographic Method;

2.Bio-marker tested: pepsinogen I (PG I) & II (PG I);

3.Clinical Sample: whole blood,  serum or plasma;

4.Other Specifications: in vitro, quantitative test;

【Clinical significance】

1. Detection of pepsinogen I (PG I) & II (PG I) simultaneously in one-single test, and calculating the ratio of PGI/PGII.

2. Diagnosis and therapeutic monitoring of chronic atrophic gastritis, gastric ulcer, and duodenal ulcer.

3. Screening of probable gastric carcinoma.

4. Efficacy evaluation of anti-Helicobacter Pylori therapy.


1. Advanced: time-resolved fluorescence immunoassay quantitative chromatography;

2. Quantitative: quantitative detection of Pepsinogen Iⅈ

3. Accurate: well correlated with imported chemiluminescence reagent (r> 0.975) ;

4. High sensitivity: lower detection limit <1.0 ng/mL ;

5. Simple: simple operation, suitable for bedside detection;

6. Widely applicable : outpatient laboratory, emergency laboratory, medical center, cardiology, ICU, and etc;


April 2014

Lumigenex receives CFDA approval for four POCT immunoassay kits to help physicians quickly and accurately diagnose heart diseases.

March 2014

Lumigenex receives CFDA approval for five immunoassay reagents adaptable to most chemical analyzers.

February 2014

Lumigenex received CFDA approval for time-resolved fluorescence immunochromatographic analyzer.

January 2014

Dr. He Aimin was named "National Thousand Talents Program"

December 2013

Lumigenex access to "high-tech enterprises in Jiangsu Province" title.

September 2013

Lumigenex passed The first Food and Drug Administration by the Suzhou Municipal Quality Management System Assessment.