50ng/ML Myocardial Infarction Test Cassette Diagnosis Of Myocardial Infarction MI
Brand Name:Citest
Certification:CE
Model Number:CMY-402
Minimum Order Quantity:N/A
Delivery Time:2-4 Weeks
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Diagnosis Myocardial Infarction Test Cassette, diagnosis of
myocardial infarction (MI)
| Principle | Chromatographic Immunoassay |
| Format | Cassette |
| Specimen | WB/S/P |
| Certificate | CE |
| Reading Time | 10 minutes |
| Pack | 10 T |
| Storage Temperature | 2-30°C |
| Shelf Life | 2 Years |
| Sensitivity | >99.9 |
| Specificity | 97.20% |
| Accuracy | 97.50% |
| Cut-Off | 50 ng/mL |
A rapid test for the diagnosis of myocardial infarction (MI) to detect qualitatively CE certified
Applications:
The Myoglobin Rapid Test Cassette (Whole Blood/Serum/Plasma) is a
rapid chromatographic immunoassay for the qualitative detection of
human Myogobin in whole blood, serum or plasma as an aid in the
diagnosis of myocardial infarction (MI).
Description:
Myoglobin (MYO) is a heme-protein normally found in skeletal and
cardiac muscle with a molecular weight of 17.8kDa.It constitutes
about 2 percent of total muscle protein and is responsible with
transporting oxygen within the muscle cells.1 When the muscle cells
are damaged, Myoglobin is released to the blood rapidly due to its
relatively small size. Following the death of tissue associated
with MI, Myoglobin is one of the first markers to rise above normal
levels.
The level of Myoglobin increases measurably above baseline within
2-4 hours post-infarct, peaking at 9-12 hours and returning to
baseline within 24-36 hours.2,3 A number of reports suggest the
measurement of Myoglobin as a diagnostic aid in confirming the
absence of myocardial infarction with negative predictive values of
up to 100% reported at certain time periods after onset of
symptoms.
The Myoglobin Rapid Test Cassette (Whole Blood/Serum/Plasma) is a
simple test that utilizes a combination of anti-Myoglobin antibody
coated particles and capture reagents to qualitatively detect
Myoglobin in whole blood, serum or plasma. The minimum detection
level is 50ng/mL.
How to use?
Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove
the test cassette from the sealed pouch and use it within one hour.
2. Place the cassette on a clean and level surface.
For Serum or Plasma specimen:
· Hold the dropper vertically and transfer 2 drops of serum or plasma (approximately 50µL) to the specimen area, then add 1 drop of buffer (approximately 40µL), and start the timer. See illustration below.
For Venipuncture Whole Blood specimen:
· Hold the dropper vertically and transfer 3 drops of whole blood (approximately 75µL) to the specimen area, then add 1 drop of buffer (approximately 40µL), and start the timer. See illustration below.
For Fingerstick Whole Blood specimen:
· To use a capillary tube: Fill the capillary tube and transfer approximately 75µL of fingerstick whole blood specimen to the specimen area of test cassette, then add 1 drop of buffer (approximately 40µL) and start the timer. See illustration below.
· To use hanging drops: Allow 3 hanging drops of fingerstick whole blood specimen (approximately 75µL) to fall into the specimen area of test
cassette, then add 1 drop of buffer (approximately 40 μL) and start the timer. See illustration below.
3. Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 20 minutes.
INTERPRETATION OF RESULTS
(Please refer to the illustration above)
POSITIVE:* A colored line in the control line region (C) and the presence of
one colored line in the test line region indicates a positive
result. This indicates that the concentration of Myoglobin is above
the minimum detection level.
*NOTE: The intensity of the color in the test line region will vary
depending on the concentration of Myoglobin, present in the
specimen. Therefore, any shade of color in the test line region
should be considered positive.
NEGATIVE: One colored line appears in the control line region (C). No line appears in the test line region (T).This indicates that
the concentration of Myoglobin is below the minimum detection
level.
INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques
are the most likely reasons for control line failure. Review the
procedure and repeat the test with a new test. If the problem
persists, discontinue using the test kit immediately and contact your local distributor.
Order Information
| Cat. No. | Product | Specimen | Pack |
| CMY-402 | Myoglobin Rapid Test | WB/S/P | 10T |
50ng/ML Myocardial Infarction Test Cassette Diagnosis Of Myocardial Infarction MI
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