Pct

Product Details:
Brand: Boditech Med Incorporated
Size : 25 T
Samples : human whole blood/serum/plasma
Specimen volume ; 150 microliter
stored at 4-30 DegreeC
Cat No : CFPC-23-1
PCT
Assessing initial risk of bacterial infection and fatal sepsis

Diagnosis of sepsis is routinely performed in intensive care units (ICU) of all hospitals. Early detection of sepsis is very important in determining appropriate treatment as it is known to improve patient survival through a various therapeutic strategy for sepsis. The ichroma & AFIAS PCT test helps detect bacterial sepsis and assess the risk of developing septic shock.

INTENDED USE :

ichroma PCT is a fluorescence Immunoassay (FIA) for the quantitative determination of Procalcitonin (PCT) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of bacterial infection and sepsis.

For in vitro diagnostic use only.

PRINCIPLE :


The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.

The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PCT concentration in sample.

STORAGE AND STABILITY:

The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately.

MATERIALS SUPPLIED :


REF CFPC-23

Components of ichromaâ?¢ PCT Cartridge Box:

- Cartridges 10

- ID Chip 1

- Instruction For Use 1 Box containing Detection Buffer tubes

- Detection Buffer Tubes 10

The One Step Test for PCT (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine PCT in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify PCT specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of PCT.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of PCT is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The cardiac troponin i fast test kit (colloidal gold) is intended for use together with the fia8000 quantitative immunoassay analyzer (fia8000). The product employs colloidal gold immunochromatogrphy to determine ctni in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify ctni specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of ctni.

Then insert test card into the fia8000 quantitative immunoassay analyzer, the concentration of ctni is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for NT-proBNP (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NT-proBNP in human serum, plasma, or whole blood specimens. One monoclonal antibody and one polyclonal antibody are employed to identify NT-proBNP specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NT-proBNP.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NT-proBNP is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for NAGL (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NGAL in human urine specimen. Monoclonal antibody and polyclonal antibody are employed to identify NGAL specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NGAL.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NGAL is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for B2-MG (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine B2-MG in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify B2-MG specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of B2-MG.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of B2-MG is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.