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Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I

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Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I

Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I
Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I

Large Image :  Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I

Product Details:
Place of Origin: China
Brand Name: Lumigenex
Certification: ISO13485, cFDA, CE
Model Number: T2009-020, T2009-050
Payment & Shipping Terms:
Minimum Order Quantity: 1250 tests
Price: USD 2.0/ Test
Packaging Details: 20 tests/box, 50 tests/box
Delivery Time: 2-10 Days
Payment Terms: T/T, Western Union, Paypal
Supply Ability: 100,000 tests/day

Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I

Description
Product Name: Cardiac Troponin I / Creatine Kinase Isoenzyme / Myoglobin (cTnI / CK-MB / Myo) Combo Test Kit (TRFIA) Funtion: Cardiac Marker
Technology: Time Resolved Fluorescence Immunochromatographic Assay (TRFIA) Usage: Vitro Diagnostic Reagent
Format: Strip, Cassette Specimen: Whole Blood, Plasma, Serum
Storing Temperature: 2℃-8℃ Shelf Life: 18 Months
Reading Time: 15 Min. Compatible Equipment: Lumigenex TRFIA Analyzer LTRIC-600, LTRIC-1000
High Light:

Cardiac Troponin I Combo Test Kit

,

Myo Combo Test Kit

,

ISO13485 Combo Test Kit

(CTnI/CK-MB/Myo) Combo Test Kit Creatine Kinase Isoenzyme Test Myoglobin Test Cardiac Troponin I Test

Cardiac Troponin I / Creatine Kinase Isoenzyme / Myoglobin (CTnI / CK-MB / Myo) Rapid Test Kit Cardiac Troponin I

High sensitivity cFDA approved 

Cardiac Troponin I / Creatine Kinase Isoenzyme / Myoglobin (cTnI / CK-MB / Myo) Combo Test Kit (TRFIA)

 
 
Intended Use
This cTnI/CK-MB/MYO Test Kit (TRFIA) is used in vitro to detect cardiac troponin I, creatine kinase isoenzyme, and myoglobin in human serum/plasma/whole blood.
The measurement of cardiac troponin I (cTnI) may help in the diagnosis of an acute myocardial infarction (AMI). Clinical investigations have shown that cardiac troponin I may be identified in the blood 4-6 hours after an AMI and can stay high for many days. Because of its myocardial specificity and sensitivity, cTnI may be utilized as a gold standard for diagnosing AMI. Creatine kinase isoenzyme (CK-MB) is widely used as a diagnostic marker of myocardial injury in the detection of acute myocardial infarction (AMI). Clinical studies have shown that CK-MB is released into blood circulation during myocardial injury and peaks within 12~24 hours and returns to normal level within 48~72 hours. Therefore, the detection of CK-MB has great clinical significance for the diagnosis of AMI. Myoglobin (abbreviated MYO) is an early indicator of myocardial necrosis. Myoglobin may be found in clinical tests within 1 hour after start and peaks in 45 hours. However, myoglobin levels increase in several situations, including skeletal muscle damage, skeletal muscle or neuromuscular dysfunction, cardiac shunt surgery, renal failure, and high-intensity physical activity. As a result, myoglobin elevation must be utilized as an auxiliary diagnosis of acute myocardial infarction (AMI) with other cardiac markers, electrocardiogram (ECG), clinical symptoms and signs, and so on. Chemiluminescence, enzyme immunoassay, fluorescence immunoassay, and colloidal gold assay are now used to detect the levels of cTnI, CK-MB, and MYO in blood samples.
Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I 0Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I 1
 
Clinical Significance

1. "Golden Standard" to diagnose myocardial infarction (MI)
2. Assess infarct size and ACS risks
3. Diagnose reinfarction or infarct extension
4. Diagnosis of myocardial injury in the perioperative period and perinatal period
5. As myocardial infarction (AMI) early detection indicator, highly sensitive
6. Diagnose reinfarction or infarct extension
7. Determine myocardial reperfusion

 

Advantages

1. Advanced: time-resolved fluorescence immunoassay quantitative chromatography
2. Quantitative: quantitative detection of cardiac troponin I (cTnI), creatine kinase (CK-MB) and myoblobin (MYO)
3. Accurate: well correlated with imported chemiluminescence reagent (r> 0.975)
4. High sensitivity: lower detection limit <0.05 ng/mL (cTnI) , <0.25 ng/mL (CK-MB) and <1.0 ng/mL (MYO)
5. Simple: simple operation, suitable for bedside detection
6. Widely applicable : outpatient laboratory, emergency laboratory, medical center, cardiology, ICU, and etc

 
Specification

Product Name
Cardiac Troponin I / Creatine Kinase Isoenzyme / Myoglobin (cTnI / CK-MB / Myo) Combo Test Kit 
Method
Time-Resolved Fluorescence Immunochromatographic Assay (TRFIA)
Certificates
ISO13495, CE
Usage
Vitro Diagnostic Reagent
Function
Cardiac Marker
Specimen
Whole Blood/ Serum/ Plasma
Test Kit Components
20 / 50 Test cards
20 / 50 Sample buffer
1 IC card
1 Instruction manual
Storage & Shelf Life
4℃-30℃, 18 months
Compatible Equipment
Lumigenex Time-resolved Fluorescence Immunoanalyzer LTRIC-600, LTRIC-1000
Test Procedure

Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I 2
Performance

Accuracy
Deviation from the quality control target value should be within ±15%.
Minimum detection limit
no higher than 0.1ug/mL.
Linearity
(0.2-50) ug/mL, the kit correlation coefficient R≥0.99
Repeatability
Coefficient of variation (CV) ≤15%.
Inter-batch difference
Inter-batch variation coefficient (CV) ≤15%.

 

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Combo Test Kit for Creatine Kinase Isoenzyme / Myoglobin / Cardiac Troponin I 3

 
Time-Resolved Fluorescence Immunoassay Analyzer
 
Product model LTRIC-600, LTRIC-1000
 
Test Menu
Cardiovascular Disease: cTnI, CK-MB, Myo, cTnI/CK-MB/MYO, H-FABP, cTnI/H-FABP, NT-proBNP, D-Dimer
Inflammation: PCT, CRP, SAA, CRP/SAA
Renal Injury: NGAL, ACR
Others: PGI/PGII, β-HCG, Influenza A+B
 
Highlights
* Nano-Enhanced Time Resolved Fluorescence Immunochromatographic Assay
* Rapid and accurate quantitative POCT Platform
* Repeatability: CV<10%
* Stability: σ ≤ 10% * Accuracy: Δn ≤ 10% * Linearity: r ≥ 0.99
 
Detection Projects
Test Strips and Cassettes (with links)

Diabetes

HbA1C, Glucose,  Ketone Body

Hyperlipidemia

Lipid Panel

Anemia

Hemoglobin

Cardiac

CK-MB, cTnI, Myo, NT-proBNP, D-Dimer, H-FABP, sST2, Homocysteine,

cTnI/H-FABP, cTnI/CK-MB/Myo

Inflammation

CRP,  PCT,  SAA,  CRP/SAA,  PCT/IL-6

Hormone

5(OH)D3, β-HCG, AMH

Gastric Function

PGI/PGII

Liver Injury

Aspartate Transaminase, Alanine Aminotransferase

Renal Injury

mALB, Creatinine, NGAL, ACR(TRFIA), ACR(Colloidal Gold)

Gout

Uric Acid

Others

Influenza A+B Combo, Influenza A+B/RSV Combo

Monkeypox CG, Monkeypox IgG/IgM, Monkeypox RT-PCR

 

Contact Details
Lumigenex (Suzhou) Co. Ltd

Contact Person: Bonnie

Tel: 86-13814877381

Send your inquiry directly to us (0 / 3000)