troponin I & CK-MB & myoglobin rapid test kits

TROPONIN I RAPID TEST CASSETTE
For the qualitative assessment of cardiac troponin I in human serum, plasma or whole blood

INTENDED USE:
Rapid TnI test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of cardiac troponin I (cTnI) in human serum or plasma specimens as an aid in the diagnosis of myocardial infarction.

SPECIFICATION:
1) Specimen: whole blood/serum/plasma
2) Format: cassette
3) Sensitivity: 99.1%
4) Specificity: 98.9%

FEATURE:
1) Simple: simply add specimen and dilution(if necessary) into sample well
2) Rapid: results come out at 15 minutes
3) Visually interpreted: donÿ¥t need any equipment
4) Stable: more than 12 month period of validity

PACKING:
Cassette: 25 tests/box, 50 tests/box

PROCEDURE:
1) Bring all materials and specimens to room temperature.
2) Remove the test card from the sealed foil pouch.
3) Use micropipetter to transfer 150 ?Yacute;L of sample, or place the transfer pipette supplied with the device in the specimen and depress the bulb to withdraw a sample.
4) Hold the pipette in a vertical position over the sample well of the test card and deliver 3-4 drops(120-160 ?Yacute;L) of sample into the sample well.
5) Read the result at 15 minutes.

PRINCIPLE:
Rapid Tn I test is a sandwich immunoassay. When sample is added to sample pad, it moves through the conjugate pad and mobilizes gold anti-cTnI conjugate that is coated on the conjugate pad. The mixture moves along the membrane by capillary action and reacts with anti-cTnI antibody that is coated on the test region. If cTnI is present at levels of 0.11 ng/mL (Bayer ACS: 180) or 1.5 ng/mL (Abbott AxSYM) or greater*, the result is the formation of a colored band in the test region. If there is no cTnI in the sample, the area will remain colorless. The sample continues to move to the control area and forms a pink to purple color, indicating the test is working and the result is valid.



CK-MB RAPID TEST
For the qualitative assessment of human CK-MB in human serum, plasma or whole blood

INTENDED USE:
Rapid CK-MB test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of CK-MB in human serum specimens as an aid in the diagnosis of myocardial infarction.

SPECIFICATION:
1) Specimen: whole blood/serum/plasma
2) Format: cassette
3) Sensitivity: 7.0 ng/ml

FEATURE:
1) Simple: simply add specimen and dilution(if necessary) into sample well
2) Rapid: results come out at 10 minutes
3) Visually interpreted: donÿ¥t need any equipment
4) Stable: more than 12 month period of validity

PACKING:
Cassette: 25 tests/box, 50 tests/box

PROCEDURE:
1) Bring all materials and specimens to room temperature.
2) Remove the test card from the sealed foil pouch.
3) Place the transfer pipette in the specimen and depress the bulb to withdraw a sample.
4) Hold the pipette in a vertical position over the sample well of the test card and deliver 2-3 drops(100-150 ?Yacute;l) of sample into the sample well.
5) Read the result at 10 minutes.

PRINCIPLE:
Rapid CK-MB test is a sandwich immunoassay. When serum sample is added to sample pad, it moves through the conjugate pad and mobilizes gold anti-CK-MB conjugate that is coated on the conjugate pad. The mixture moves along the membrane by capillary action and reacts with anti-CK-MB antibody that is coated on the test region. If CK-MB is present at levels of 7.0 ng/ml or greater, the result is the formation of a colored band in the test region. If there is no CK-MB in the sample, the area will remain colorless. The sample continues to move to the control area and forms a pink to purple color, indicating the test is working and the result is valid.



RAPID MYOGLOBIN TEST CASSETTE
For the qualitative assessment of human myoglobin in human serum, plasma or whole blood

INTENDED USE:
Rapid Myoglobin test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of myoglobin in human serum specimens. The presence of myoglobin in serum or plasma specimens at level 100 ng/ml or higher can be detected in 10 minutes.

SPECIFICATION:
1) Specimen: whole blood/serum/plasma
2) Format: cassette
3) Sensitivity: 7.0 ng/ml

FEATURE:
1) Simple: simply add specimen and dilution(if necessary) into sample well
2) Rapid: results come out at 10 minutes
3) Visually interpreted: donÿ¥t need any equipment
4) Stable: more than 12 month period of validity

PACKING:
Cassette: 25 tests/box, 50 tests/box

PROCEDURE:
1) Bring all materials and specimens to room temperature.
2) Remove the test card from the sealed foil pouch.
3) Use micropipetter to transfer 150 ?Yacute;l of sample, or place the transfer pipette supplied with the device in the specimen and depress the bulb to withdraw a sample.
4) Hold the pipette in a vertical position over the sample well of the test card and deliver 3-4 drops (120-160 ?Yacute;l) of sample into the sample well.
5) Read the result at 10 minutes.

PRINCIPLE:
Rapid Myglobin test is a sandwich immunoassay. When serum sample is added to sample pad, it moves through the conjugate pad and mobilizes gold anti-myoglobin conjugate that is coated on the conjugate pad. The mixture moves along the membrane by capillary action and reacts with anti-myoglobin antibody that is coated on the test region. If myoglobin is present at levels of 100 ng/ml or greater, the result is the formation of a colored band in the test region. If there is no myoglobin in the sample, the area will remain colorless. The sample continues to move to the control area and forms a pink to purple color, indicating the test is working and the result is valid.