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PG I Rapid Quantitative Test Kit IFA Colloidal Gold CE Approval IVD Blood Diagnostic

PG I Rapid Quantitative Test Kit IFA Colloidal Gold CE Approval IVD Blood Diagnostic

Place of Origin:

CN

Brand Name:

WWHS

Certification:

CE

Model Number:

PGI

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Product Details
Product Name:
PG I Rapid Quantitative Test Kit
Type:
One Step Assay
Reactivity:
Human
Formal Name:
Thyroxine
Manufacturer:
WWHS Biotech INC
Advantage:
High Sensitivity
Throughput:
3000 Tests/Day
Format:
Cassette
Usage:
Tumor Marker
Keywords:
High Stability, High Accuracy
Payment & Shipping Terms
Minimum Order Quantity
1000
Price
US 1.50 - 2.50 Kit
Packaging Details
Colorful Paper Box
Delivery Time
7 Days
Payment Terms
T/T
Supply Ability
30000 Kits per Week
Product Description

PG I Rapid Quantitative Test Kit IFA Colloidal Gold CE Approval IVD Blood Diagnostic

 

Phosphoglucose isomerase (glucose-6-phosphate isomerase or PGI, EC 5.3.1.9) is an important housekeeping enzyme. PGI catalyzes the interconversion of glucose-6- phosphate to fructose-6-phosphate. PGI performs multiple functions & intracellularly plays key role in both glycolysis and gluconeogenesis. Extracellularly, PGI [also called Autocrine Motility Factor (AMF)] functions as a cytokine, which stimulates cell motility and is associated with tumor development and metastasis. In humans, PGI deficiency causes hemolytic anemia, whereas increased PGI activity is observed in many cancers such as gastrointestinal, kidney and breast cancer. Early detection of abnormal phosphoglucose isomerase activity is crucial for diagnosis, prediction and therapeutic strategy.

 

About NIR-1000 Dry Fluoroimmunoassay Analyser

 

It is a fluorescence immunochromatographic analysing system with internal temperature control,
which can help diagnose conditions such as infection, diabetes, cardiovascular diseases, renal injury and cancers, etc.
Immunofluorescence technology
Testing time less than 15 minutes
Easy-to-use touch-screen platform,multi-language system

 

Note:


1) Any variation in operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in
result. Each user should obtain their own standard curve.

2) If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.
3) If specimens generate values higher than the highest standard, dilute the specimens and repeat the assay

 

Assay list  Tumor Marker        
cat#. Product item Specimen Reaction Time Measure Range Clinical Range Itended Use
20 AFP Serum/Plasma 15min. 2.5-200ng/ml <20ng/ml pregnancy cancer
21 CEA Serum/Plasma 15min. 1-200ng/ml <5ng/ml colon cancer, colorectal cancer,etc.
22 NSE Serum/Plasma 15min. 1-400ng/ml <16ng/ml non-small cell lung cancer
23 FOB fecal specimens 10min. 50-1000ng/ml <100ng/ml Abnormal recessive gastrointestinal bleeding
24 PG II Serum/Plasma 15min. 1-100ug/L PGI/PGII>3.0 gastric abnormalities
25 PG I Serum/Plasma 15min. 2.5-200ug/L >70ng/ml gastric abnormalities
26 TPSA Serum/Plasma 15min. 0.5-40ng/ml <4ng/ml prostate cancer
27 FPSA Serum/Plasma 15min. 0.1-10ng/ml <1ng/ml prostate cancer
28 CA12-5 Serum/Plasma 15min. 20-500U/ml <35U/ml ovarian cancer
29 CA15-3 Serum/Plasma 15min. 10-400U/ml < 25 U/mL breast cancer
30 HE4 Serum/Plasma 15min. 50-2000pmol/L <140 pmol/L ovarian cancer
31 CA19-9 Serum/Plasma 15min. 10-400U/ml < 27 U/mL pancreatic cancer
32 β-HCG Serum/Plasma 15min. 5-400mIU/ml <10 mIU/mL Early pregrancy, ectopic HCG cancer,incomplete abortion
33 CK19(Cyfra21-1) Serum/Plasma 15min. 0.5-50ng/ml <2.5ng/ml non-small cell lung cancer

 

 

PG I Rapid Quantitative Test Kit IFA Colloidal Gold CE Approval IVD Blood Diagnostic 0PG I Rapid Quantitative Test Kit IFA Colloidal Gold CE Approval IVD Blood Diagnostic 1

 

 

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