Digestive System Disease Diagnosis

PG-I/PG-II 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 I&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 


Mar. 2014

CFDA approvals for five immunoassay reagents adaptable to most chemical analyzers were obtained

Feb. 2014

CFDA approvals for time-resolved fluorescence immunochromatographic analyzer were obtained

Sep. 2013

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