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Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical

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Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical

Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical
Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical

Large Image :  Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical

Product Details:
Place of Origin: China
Brand Name: Lumigenex
Certification: ISO13485, cFDA, CE
Model Number: T2015-020, T2015-050
Payment & Shipping Terms:
Minimum Order Quantity: 1250 tests
Price: USD 3.0/ 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

Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical

Description
Product Name: C-Reactive Protein/Serum Amyloid A (CRP/ SAA) Combo Test Kit Test Kit (TRFIA) Funtion: Inflammation 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:

Serum Amyloid A Rapid Detection Kit

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C-Reactive Protein Rapid Detection Kit

C-Reactive Protein/Serum Amyloid A (CRP/SAA) Rapid Detection Kit TRFIA Analyzer In Hospital Clinical Laboratory

High sensitivity cFDA approved C-Reactive Protein/Serum Amyloid A (CRP/ SAA) Combo Test Kit Test Kit

 
Intended Use

This test kit (time-resolved fluorescence immunoassay) is suitable for quantitative determination of C-Reactive Protein (CRP) and Serum Amyloid A (SAA) in human serum, plasma, and whole blood in vitro.
Concentration of CRP can be used as an auxiliary diagnostic tool to assess cardiovascular disease and inflammatory response. At present, the application of CRP mainly includes the following aspects: adult postoperative stage, pulmonary infection, pediatric fever, myocardial infarction, gouty arthritis, osteoarthritis, gastrointestinal diseases, intestinal inflammatory diseases, Pediatric infectious diseases, etc.
SAA is an acute-phase protein, Its detection helps to diagnose inflammation and assess acute phase reaction processes. During inflammatory, infectious and non-infectious diseases, its concentration in the blood can rise sharply within hours. SAA is associated with high-density lipoprotein (HDL), which regulates HDL metabolism during inflammation. SAA degradation products can be deposited in different organs in the form of amyloid A fibrils, which is a serious complication in chronic inflammatory diseases.
 
Advantages

1. Advanced: time-resolved fluorescence immunoassay quantitative chromatography
2. Quantitative: quantitative detection of CRP/ SAA
3. Accurate: well correlated with imported chemiluminescence reagent (r> 0.975)
4. High sensitivity: lower detection limit <1.0 ng/mL
5. Simple: simple operation, suitable for bedside detection
6. Widely applicable : outpatient laboratory, emergency laboratory, medical center, cardiology, ICU, and etc.
Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical 0Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical 1
Specification

Product Name
C-Reactive Protein/Serum Amyloid A (CRP/ SAA) Combo Test Kit Test Kit (TRFIA)
Method
Time Resolved Fluorescence Immunochromatographic Assay (TRFIA)
Certificates
ISO13495, CE
Usage
Vitro Diagnostic Reagent
Function
Inflammation 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
Unopened test kit is stable for 18 months under 2-8℃, and up to 30 days under 2-30℃.
Temperature change (< 37℃) during shipment has no effect on quality of the test kit.
Unsealed test kit is stable within 1 hour
Compatible Equipment
Lumigenex Time-resolved Fluorescence Immunoanalyzer LTRIC-600, LTRIC-1000
Test Procedure

Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical 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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Serum Amyloid A / C-Reactive Protein Rapid Detection Kit In Clinical 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 TRIFA
* 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)