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TRI Antibody Rapid Test Cassette Whole Blood / Serum /Plasma Specimen, detection of antibodies to Trichinella
Principle
Chromatographic Immunoassay
Format
Cassette
Specimen
Whole Blood/Serum/Plasma
Reading Time
5-10 minutes
Pack
10 T
Storage Temperature
2-30°C
Shelf Life
2 Years
Sensitivity
89.36%
Specificity
92.45%
Accuracy
91.00%
APPLICATION
The TRI Antibody Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Trichinella in swine’s whole blood or serum and plasma.
PRINCIPLE
The TRI Antibody Rapid Test Cassette (Whole Blood/Serum/Plasma) is a qualitative, membrane based immunoassay with a double antigen system for the detection of Trichinella antibodies in serum or plasma. The membrane is pre-coated with recombinant TRI antigens. The test cassette has a testing window. The testing window has an invisible T (test) line region and C (control) line region. During testing, antibodies to TRI, if present in whole blood, serum or plasma specimen react with TRI antigen coated colloidal gold particles in the test strip.
The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with recombinant TRI antigens on the membrane in the test line region. If the specimen contains antibodies to trichinella, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain trichinella antibodies, a colored line will not appear in the test line region indicating a negative result. To serve as a procedural control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
MATERIALS
Materials Provided
• Test cassettes
• Droppers
• Package insert
• Buffer
Materials Required But Not Provided
• Specimen collection containers
• Centrifuge (for plasma only)
• Timer
DIRECTIONS FOR USE
Allow the test cassette, specimen, buffer, and/or controls to equilibrate to room temperature (15-30 °C) prior to testing.
1.Remove the test cassette from the foil pouch and use it as soon as possible. Best results will be obtained if the assay is performed within one hour.
2. Collect swine’s fresh whole blood or separate serum or plasma from blood as soon as possible to avoid hemolysis. Only use clear, non-hemolyzed specimens. Do not leave the specimens at room temperature for prolonged periods. Serum and plasma specimens may be stored at 2-8 °C for up to 3 days. For long term storage, specimens should be kept below -20 °C.
3.Place the test cassette on a clean and level surface.
4.For serum and plasma: Hold the dropper vertically and draw the specimen up to the Fill Line (approximately 5 µL), and transfer the specimen to the specimen well (S) of the test cassette, wait for 8-10 seconds, then add 2 drops of buffer (approximately 80 µl) and start the timer. For whole blood: Hold the dropper vertically, draw the specimen above 1cm above the Fill Line, and transfer 1 drop of whole blood (approximately 10 µL) to the specimen well (S) of the test cassette, wait for 8-10 seconds, then add 2 drops of buffer (approximately 80 µL) and start the timer.
5. Read the result in 5-10 minutes. Do not interpret results after 15 minutes.
INTERPRETATION OF RESULTS
Positive: The presence of both C line and T line, regardless of T line being strong or faint.
Negative: Only clear C line appears.
Invalid: No colored line appears in C line region, regardless of T line’s appearance.
Cat. No.
Product
Specimen
Pack
VITR-402
TRI Antibody Rapid Test
Whole Blood/Serum/Plasma
10T
Company Details
Bronze Gleitlager
,
Bronze Sleeve Bushings
and
Graphite Plugged Bushings
from Quality China Factory
Business Type:
Manufacturer,Exporter,Trading Company
Total Annual:
80000000-100000000
Employee Number:
500~10000
Ecer Certification：
Verified Supplier
CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies.
... CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies.
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