Snibe MAGLUMI hs-Troponin I (CLIA)

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Product Details:

Accuracy Within manufacturers specified CV <10%
Function Cardiac biomarker detection
Storage Instructions 2~8C, avoid freezing
Shelf Life 12 months
Features High sensitivity, Fast turnaround time, Wide linear range, Reliable performance
Usage Type In-vitro Diagnostic (IVD) reagent
Instruments Type MAGLUMI Series Automated Immunoassay Analyzer
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Snibe MAGLUMI hs-Troponin I (CLIA) Price And Quantity

Pack Size List of 100 or 200 tests per kit (varies by catalog no.)
Hazard Information Non-hazardous under normal laboratory use
Test Duration ~18 minutes per test (on MAGLUMI platform)
Calibration Interval Recommended per analyzer guidelines, typically every 28 days or as needed
Test Principle Two-site sandwich chemiluminescence immunoassay
Sample Type Serum or Plasma
Intended Use Detection and management of acute myocardial infarction (AMI) and other cardiac conditions
Reagent Format Ready-to-use liquid reagents
Compatibility Compatible with all Snibe MAGLUMI platforms
Limit of Detection 0.01 ng/mL

Snibe MAGLUMI hs-Troponin I (CLIA) Product Specifications

Technology Chemiluminescence Immunoassay (CLIA)
Material Diagnostic Reagent, Microbeads, Antibodies, Buffer Solution
Shelf Life 12 months
Features High sensitivity, Fast turnaround time, Wide linear range, Reliable performance
Equipment Type Immunoassay Analyzer Reagent Kit
Usage Type In-vitro Diagnostic (IVD) reagent
Measurement Range 0.150 ng/mL
Instruments Type MAGLUMI Series Automated Immunoassay Analyzer
Portable No (for use with laboratory analyzer)
Accuracy Within manufacturers specified CV <10%
Real-Time Operation Yes
Function Cardiac biomarker detection
Storage Instructions 2~8C, avoid freezing
Power Source Not Applicable (for reagent kit; compatible with MAGLUMI automated analyzers)
Wall Mounted No
Use Quantitative determination of S-Troponin I in human serum or plasma
Operating Type Automated
Condition New
Color Colorless (Solution)

Pack Size List of 100 or 200 tests per kit (varies by catalog no.)
Hazard Information Non-hazardous under normal laboratory use
Test Duration ~18 minutes per test (on MAGLUMI platform)
Calibration Interval Recommended per analyzer guidelines, typically every 28 days or as needed
Test Principle Two-site sandwich chemiluminescence immunoassay
Sample Type Serum or Plasma
Intended Use Detection and management of acute myocardial infarction (AMI) and other cardiac conditions
Reagent Format Ready-to-use liquid reagents
Compatibility Compatible with all Snibe MAGLUMI platforms
Limit of Detection 0.01 ng/mL

Product Description

Brand	Snibe
Sample Type	Serum
Pack Size	100T
CAT No.	13020609M
Application	Infection

The kit has been designed for the quantitative determination of Troponin I (high sensitive) in human serum. The method can be used for samples over the range of 0-50ng/ml. The test has to be performed on the MAGLUMI chemiluminescence immunoassay (CLIA) fully auto analyzer (Including MAGLUMI 1000, MAGLUMI 2000, MAGLUMI 2000 Plus and new developed models).

Precision Cardiac Biomarker Analysis

Snibe MAGLUMI S-Troponin I enables laboratories to provide accurate, real-time cardiac biomarker detection for rapid clinical decision-making. Its advanced chemiluminescence technology and automated process ensure dependable results for patient management in acute cardiovascular emergencies.

User-Friendly and Reliable Performance

Designed with convenience in mind, the kit comes as a ready-to-use liquid format, requiring no elaborate preparation. Automated operation on the MAGLUMI analyzers ensures ease of use, minimal hands-on time, and consistent performance within a 12-month shelf life.

Adaptable to Laboratory Workflows

The reagent kit is suitable for diverse laboratory environments across India, serving dealers, suppliers, and healthcare facilities. Its compatibility with all MAGLUMI analyzers and standard storage conditions (2-8C) makes it accessible and flexible for varying testing volumes.

FAQ's of Snibe MAGLUMI S-Troponin I (CLIA):

Q: How does the Snibe MAGLUMI S-Troponin I (CLIA) detect Troponin I in samples?

A: The kit uses a two-site sandwich chemiluminescence immunoassay, which specifically binds S-Troponin I in human serum or plasma, allowing quantitative detection through MAGLUMI automated immunoassay analyzers.

Q: What is the recommended calibration schedule for this test kit?

A: Calibration should be performed according to analyzer guidelines, typically every 28 days or more frequently as indicated by quality control results.

Q: Where is the Snibe MAGLUMI S-Troponin I kit typically used?

A: This reagent kit is intended for use in clinical laboratories equipped with MAGLUMI Series Automated Immunoassay Analyzers. It is not portable and is suitable for in-vitro diagnostic use in hospitals and diagnostic centers.

Q: When can test results be expected after sample loading?

A: Results are typically available in about 18 minutes per test cycle when running on a MAGLUMI platform.

Q: What are the benefits of using this kit for acute myocardial infarction management?

A: It provides high sensitivity and reliability, enabling early detection of cardiac events. Fast turnaround times support prompt clinical assessment and improved patient outcomes.

Q: How should the reagent kit be stored to maintain stability?

A: The reagents should be stored at 2-8C, avoiding freezing, to ensure optimal shelf life and assay performance.

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