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PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD

PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD

Fluorescence Immunoassay Test Kit

PGI Rapid Test Kit

POCT PGI Rapid Test Kit

Place of Origin:

CN

Brand Name:

WWHS

Certification:

ISO 13485, CE

Model Number:

PG-I

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Product Details
Product Name:
PGI Rapid Test Kit
Sample Buffer:
25 Vials
Usage:
Tumor Marker
Storage:
RT
Warranty:
12 Months
Formal Name:
Pepsinogen I
Advantage:
High Sensitivity
Application In:
WWHS NIR-1000
Format:
Cassette
Reaction Time:
15 Min.
Payment & Shipping Terms
Minimum Order Quantity
1000
Price
US 1.50-2.50 Kit
Packaging Details
Colorful Paper Box
Delivery Time
10 Days
Payment Terms
L/C, T/T
Supply Ability
30000 Kits per Week
Product Description

PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD

 

Human pepsinogens I (PGI) and II (PGII) are proenzymes of pepsin—an endoproteinase of gastric juice.

PGI is secreted mainly by chief cells in the fundic mucosa, whereas PGII is also secreted by the pyloric glands and the proximal duodenal mucosa.

 

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.

 

Characteristics


1. Accurate: Double antibody sandwich method, high sensitivity.
2. Rapid: Get results in 15 minutes.
3. Convenient: No need professional training, test could be performed at any time, any place.

 

Sample requirements


1. Plasma, serum and whole blood can be used as samples. The whole blood should be collected in a tube containing heparin, citrate or EDTA as the anticoagulant. If the serum procedure is used, collect blood in a tube without anticoagulant and allow clotting. Hemolyzed samples should not be used.
2. Venous blood was collected according to routine laboratory methods to avoid hemolysis.
3. It is highly recommended to use fresh samples instead of keeping the samples at room temperature for a long time. After samples were collected, the detection should be completed within 4 hours at room temperature (15℃~30℃). The whole blood sample can be stored at 2℃~8℃ for 24 hours. Plasma and serum samples can be stored at 2℃~ 8℃ for 7 days, -20℃for 30 days.
4. Before testing, the sample should return to room temperature (15℃~30℃). The frozen samples should be completely thawed, rewarming and mixed evenly before use. Repeated freeze-thaw cycles should be avoided.

 

Item Name Quantity Component
Test Cards 20 Strip  It is composed of fluorescent pad (coated with fluorescent labeled PG I   monoclonal mouse antibody), nitrocellulose membrane (coated with PG I   monoclonal mouse antibody and Goat anti mouse IgG antibody),   absorbent paper and backing
Sample Buffer 20(300μL/tube)  Phosphate buffer
Information Card 1 Individual  With AFP specific stand curve file

 

PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 0PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 1PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 2

PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 3PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 4PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 5PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 6PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 7PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 8

PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 9PGI Rapid Quantitative Fluorescence Immunoassay Test Kit WWHS FIA POCT IVD 10

 

WWHS 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

 

Interpretation of results


1. This reagent is only used for auxiliary detection. If the test results are abnormal, it should be reviewed in time and judged in combination with clinical symptoms.
2. For samples with AFP concentration lower than 2.5ng/ml and higher than 200ng/ml, the detection results are reported as "< 2.5ng/ml" and "> 200ng /ml", respectively.


Limitations of methods


1. This kit is only used to detect human plasma/whole blood samples
2. Due to the limitations of immunoassay methods of antigen and antibody reaction, the results cannot be used as the only basis for clinical diagnosis, but should be evaluated with all the existing clinical and experimental data.
3. The content of triglyceride in the sample shall not exceed 15mg/ml, the content of hemoglobin shall not exceed 5mg/ml, and the content of bilirubin shall not exceed 0.5mg/ml, and the relative deviation of the test results shall not exceed ±15%.
4. When the concentration of AFP in the sample is less than 20000ng/ml, there is no hook effect.
5. HAMA effect was not produced when the concentration of human anti rat in the sample was less than 50ng/ml.
6. When RF concentration in the sample is less than 2000IU/ml, the relative deviation of the test results is within ±15%.

Applicable Instrument

 

WWHS NIR-1000 dry fluoroimmunoassay analyser

 

Advantage

 

1. Advanced Quality: We have strict quality control system and enjoy good reputation in the market.

2. Sincerly Service: We treat clients as friend and aims at building long term business relatiionship.

 

FAQ

 

Q1: Are you trading company or manufacturer?
A1: We are manufacturer.

 

Q2: Do you provide samples ?
A2: Yes,we do provide samples.If you need it, please contact us.

 

Q3: How about the quality?
A3: We have the best professional engineer and strict QA and QC system to ensure you get high quality products from us.

 

Q4: How’s the package?
A4: Normally are cartons, but also we can pack it according to your requirements.

 

Q5: How’s the delivery time?
A5: It depends on the quantity you need.

 

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