Cardiac Marker Troponin I Test Cassette 50T
TROPONIN I CARD
Intended Use:
Test for qualitative detection troponin I in human whole blood, serum or plasma sample.
Introduction:
Troponin I (TnI) is part of troponin complex, which together with tropomyosin, forms the main component that regulates the Ca+2 –sensitive ATP-ase activity of actomyosin is striated muscle (skeletal and cardiac). The troponin complex consists of three subunit has a distinct function with TnC as the site of Ca+2 binding, TnT the tropomyosin binding, and Tnl as the inhibitory subunit. Different isoforms of Tnl exists in the skeletal and cardiac muscles (sTnl and cTnl, respectively) with distinct immunologic epitopes that allow the production of cardiac-specific Tnl antibodies. The cardiac marker, troponin I has been established as useful tools in the diagnosis of acute myocardial infraction (AMI). Troponin I is found in blood at elevated concentrations approximately 4-6 hours after the onset of chest pain and peak at 12-24 hours. Troponin I levels remain elevated for up to 14 days. The use if this marker is an aid in the diagnosis of AMI after myocardial function.
Principle:
The Troponin I Rapid Test Device employs a solid-phase chromatographic immunoassay technology to qualitatively detect the elevation of Troponin I in human blood samples. When a sample of blood is dispensed into the sample well, red blood cells are removed by the built in separation system. Troponin I in the specimen makes a complex with the specific dye conjugate and biotinylated anti-troponin I antibody. This complex migrates through the test area containing immobilized streptavidin. The antibody dye-troponin I-biotinylated antibody complex bind to the immobilized streptavidin in the test area. Unbound dye complexes migrate out of test area and are later captured in the Control area. Visible pinkish-purple bands will appear in the test and Control areas if the concentrations of troponin I is above established cut-off values. If the troponin I concentration in the specimen is 0.6 ng/ml or greater, a band is present in the troponin I area. If a band is present only in the Control area, the test result is read as negative, indicating that the Troponin I concentrations are all below the cut-off values. If no band is present in the Control area, the test is invalid and another test must be run, regardless of the presence or absence of band(s) in the Test Area.
Pack Size:
25 Test.
50 Test.
Kit components:
Test Device.
Assay Buffer.
Instructions for Use.
Storage Temperature:
Room Temperature (2-30 0C).
Shelf life:
24 months
Sample Type:
Whole Blood, Serum or Plasma.
Test Procedure:
Qualitative only.
Pack Size:
25 Test.
50 Test.
WHO WE ARE
Established in 1998, Anamol Laboratories Pvt. Ltd. today is synonymous with Quality and Consistency. The very name of Anamol comprises two separate words combined together as one which are “ANA” and “MOL” which means “ANALYSIS of MOLECULES”, explaining our core strength in understanding Chemistry and Biochemistry as a subject and how different molecules interact with each other. It is because of this in-depth knowledge that we can elevate our products to international standards or better. The power of current knowledge base and zeal to acquire new knowledge with the same depth and clarity has helped shape our core competency and gain trust from people within and outside the industry for close to two decades now.
WHAT WE DO?
We are highly sophisticated and professional manufacturers of Clinical Chemistry Reagents, Rapid Immunoassays, Urine Tests Strips, Immunology reagents, Dyes and Stains for Fluorometry and many others. Every product we develop, we keep in mind how we would help spread the confidence of an accurate diagnostic report to the Medical Practitioner as well as to the Patient. It is because of this goal at our hearts, we believe in adding value to the product to remain competitive and improve our Value Proposition.
OUR FACILITY
We have a state-of-the-art production facility of around 27,000 square ft. located in Palghar (Near Mumbai), Maharashtra, India which is just 100 km away from ChhatrapatiShivaji International Airport, Mumbai, India. The location is well connected to Rail, Road, Sea and Air for multiple modes of transportation of products. The entire facility has been certified by Food and Drugs Administration (Schedule M), Government of India. Our facility is GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) certified. All operations are governed through ISO 9001:2015 and ISO 13485:2003 Quality Management Systems. The latest equipments and infrastructures empowers the manufacturing of 2000 liters of liquid reagents being taken up from formulations to bottling as final product on daily basis. Current plant capacity from raw materials to finished goods exceeds 3 million tests/day. The entire manufacturing process is done is controlled environment of humidity, particle-free zones and class 10,000 production rooms. Systems and multiple auto-check points have helped ALPL to run 4 different production lines simultaneously with zero error to achieve maximum production.
VISION
To contribute in adding disease-free years in human life.
MISION
We shall strive to achieve trust of our customers by providing them dependable diagnosis through our products.
To achieve global footprint as one of the most reliable and preferred healthcare company.
VALUES
Customer Commitment:
We are concerned to meet our customer’s changing needs and expectations from time to time and to design innovative and user-friendly solutions having high value propositions to address the same.
Win-Win Relationship:
We strive to build a long-lasting and mutually beneficial collaboration with all our stakeholders.
Accountability:
We remain accountable for quality of our people & products and to work towards their betterment everyday.
Knowledge Management:
We have quest to acquire, implement and share knowledge pool with all our stakeholders.
Ethics:
Being Ethical, Honest and Transparent in our conduct is at the very root of our business. 
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