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Professional Tumor Markers Rapid Diagnostic Test Cassette for Ferritin FRT

Basic Information
Place of Origin: China
Brand Name: Dewei
Certification: ISO, CE
Model Number: FRT-DW02
Minimum Order Quantity: 3000 units
Price: Negotiable
Packaging Details: 25test/box, 40test/box
Delivery Time: in 20 days
Payment Terms: L/C, T/T, Western Union
Supply Ability: 500,000pcs/day
Detail Information
Sample: Whole Blood Type: Cassette
Certificate: ISO, CE Origin: China
Shelf Life: 24 Months Usage: Professional Use
Highlight:

Ferritin FRT Rapid Diagnostic Test Cassette

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Professional Rapid Diagnostic Test Cassette


Product Description

Ferritin (FRT) Rapid Test Tumor Markers Rapid Diagnostic Test Kit

 

A rapid, one step test for the qualitative detection of Human Ferritin in whole blood /serum/ plasma.
For professional in vitro diagnostic use only.
 
 

【INTENDED USE】

The Ferritin Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of human ferritin in human whole blood, serum and plasma.

 

 

 

【INTRODUCTION】
Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. Plasma ferritin is an indirect marker of the total amount of iron stored in the body; hence serum ferritin is used as a diagnostic test for iron deficiency anemia.
A normal ferritin blood level, referred to as the reference interval is determined by many testing laboratories. In most tissues, ferritin is a major iron storage protein. Human ferritin has a molecular weight of approximately 450,000 Daltons, and consists of a protein shell around an iron core; each molecule of ferritin may contain as many as 4,000 iron atoms. Under normal conditions, this may represent 25% of the total iron found in the body. In addition, ferritin can be found in several isomers. If the ferritin level is low, there is a risk for lack of iron, which could lead to anemia. Low ferritin may also indicate hypothyroidism, vitamin C deficiency or celiac disease. Low serum ferritin levels are seen in some patients with restless legs syndrome, not necessarily related to anemia, but perhaps due to low iron stores short of anemia.

 

 

 

【PRINCIPLE】
The Ferritin Rapid Test is a qualitative, lateral flow immunoassay for the detection of human ferritin in Whole blood/serum/plasma. The membrane is precoated with anti-ferritin antibody on the test line region of the test. During testing, the specimen reacts with the particle coated with anti-ferritin antibody. The mixture migrates upward on the membrane chromatographically by capillary action to react with anti-ferritinantibody on the membrane and generate a colored line. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear in the control line region, indicating that the proper volume of specimen has been added and membrane wicking has occurred.

 

 

 

【MAIN CONTENTS
• Rapid test with desiccant.
• Buffer
• Pipette
• Package insert
 
 
 
PRECAUTIONS
• For professional in vitro diagnostic use only.
• Do not use after expiration date indicated on package. Do not use the test if the foil pouch is damaged. Do not reuse tests.
• This kit contains products of animal origin. Certified knowledge of the origin and/or sanitary state of the animals does not completely guarantee the absence of transmissible pathogenic agents. It is therefore, recommended that these products be treated as potentially infectious, and handled by observing usual safety precautions (e.g., do not ingest or inhale).
• Avoid cross-contamination of specimens by using a new specimen collection container for each specimen obtained.
• Read the entire procedure carefully prior to testing.
• Do not eat, drink or smoke in the area where the specimens and kits are handled. Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout the procedure and follow standard procedures for the proper disposal of specimens. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed.
• Humidity and temperature can adversely affect results.
• Used testing materials should be discarded according to local regulations.
 
 

 

【STORAGE AND STABILITY】
• Store at 2 ~ 30 º C in the sealed pouch for 24 months.
• Keep away from direct sunlight, moisture and heat.
• DO NOT FREEZE.
 
 

 

【SAMPLE COLLECTION】
• Separate serum or plasma from blood as soon as possible to avoid hemolysis. Use only clear non-hemolyzed specimens.
• Testing should be performed immediately after the specimens have been collected. Do not leave the specimens at room temperature for prolonged periods. Serum and plasma specimens may be stored 2-8℃ for up to 3 days. For long term storage, specimens should be kept below -20℃ if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.
• Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
 
 
 

 

【DIRECTION OF USE
Bring tests, specimens, and/or controls to room temperature (15-30°C) before use.
1. Remove the test cassette from the sealed pouch and use it within one hour.
Using the provided disposable pipette, transfer 1 drop of Serum or Plasma specimen into the center of the specimen well(s) of the test cassette, then add 1 drop of buffer, and start the timer.
OR
Transfer 2 drops of Whole Blood specimen into the center of the specimen well(s) of the test cassette, then add 1 drop of buffer, and start the timer.
Avoid trapping air bubbles in the specimen well (S), and do not add any solution to the result area.
As the test begins to work, color will migrate across the membrane.
3. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not read results after 20 minutes.

 

 

 
【INTERPRETATION OF RESULTS
POSITIVE:
The presence of two lines as control line (C) and test line (T) within the result window indicates a positive result.
NEGATIVE:
The presence of only control line (C) within the result window indicates a negative result.
INVALID:
If the control line (C) is not visible within the result window after performing the test, the result is considered invalid. Some causes of invalid results are because of not following the directions correctly or the test may have deteriorated beyond the expiration date. It is recommended that the specimen be re-tested using a new test.
 
 
 

For further operation or performance details, please refer to final instruction manual.

 

 

 

 

Contact Details
Bonnie He

Phone Number : +8613030247038

WhatsApp : +8615267039708