Pharmaceutical Injection

Product Details:

Description The Qiagen artus Hepatitis C Virus QS-RGQ Kit is a ready-to-use molecular detection kit for the quantitative detection of Hepatitis C Virus (HCV) RNA in human plasma using real-time RT-PCR. This kit is part of the integrated QIAsymphony RGQ system, providing a complete, automated workflow from sample preparation to quantitative pathogen detection. It is designed for high accuracy, sensitivity, and specificity, enabling precise monitoring of viral load in patients undergoing antiviral treatment and aiding in disease management. The kit includes all necessary reagents for specific amplification of a region of the HCV genome and direct detection of the amplicon. An internal control (IC) system is also included to identify potential PCR inhibition, ensuring reliable results.

Note The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.

KEY FEATURES

• Quantitative Detection: Provides precise quantification of HCV RNA without standard curves.
• High Sensitivity: Optimized to detect low numbers of HCV RNA (e.g., analytical sensitivity of 21 IU/ml for version 2).
• Broad Linear Range: Detects HCV RNA over a wide concentration range (e.g., 15 IU/ml to 1 x 10$^{8}$ IU/ml for version 2).
• Internal Control (IC): Heterologous amplification system to detect PCR inhibition and monitor extraction efficiency.
• Genotype Coverage: Designed to detect HCV genotypes 1-6.
• Automated Workflow: Integrates with QIAsymphony SP/AS for automated sample preparation and assay setup.
• Real-Time RT-PCR: Utilizes real-time reverse transcription polymerase chain reaction.
• Ready-to-Use: Contains all necessary reagents for the assay.
• Validated Sample Type: Primarily validated for human EDTA plasma.
• Reliability: High levels of analytical specificity, sensitivity, and reproducibility.

Industry Served

• Clinical Diagnostics
• Molecular Diagnostics
• Virology Laboratories
• Blood Banks
• Research Institutions studying infectious diseases
• Hospitals and Reference Laboratories for patient management and viral load monitoring.

Disclaimer Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.

Product Details:

The Sartorius MD8 Air Monitoring Systems, comprising the MD8 Airscan and the portable AirPort MD8, are advanced instruments designed for the precise detection of airborne microorganisms, including bacteria, viruses, yeasts, and fungi. Utilizing unique Gelatine Membrane Filters (GMF) and BACTair agar plates, these systems ensure accurate and reliable air sampling in cleanrooms and controlled environments, meeting stringent regulatory standards.

Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263.

Key Features:

• Versatile Sampling Options: Offers both stationary (MD8 Airscan®) and portable (AirPort MD8) configurations to suit various environmental monitoring needs. 

• High-Efficiency Gelatine Membrane Filters: Employs GMFs that effectively capture even the smallest airborne microorganisms, ensuring high retention rates. 

• Adjustable Airflow Rates: AirPort MD8 allows for adjustable flow rates ranging from 10 to 125 L/min, accommodating different sampling requirements. 

• User-Friendly Interface: Features intuitive controls and displays for easy operation, including preset sampling volumes and real-time monitoring of sampling parameters. 

• Regulatory Compliance: Designed to meet international standards for air monitoring in cleanrooms, including ISO 14698 and EU GMP Annex 1 guidelines. 

Industries Served:

• Pharmaceutical Manufacturing: Ensures aseptic conditions by monitoring airborne contaminants during drug production processes.

• Biotechnology: Maintains controlled environments for sensitive biological experiments and productions.

• Food and Beverage Industry: Monitors air quality to prevent contamination during food processing and packaging.

• Healthcare Facilities: Assists in infection control by detecting airborne pathogens in hospitals and clinics.

• Environmental Monitoring: Evaluates air quality in various settings to ensure compliance with health and safety regulations.

Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.

 

Product Details:

The Nu Life Care AbChek Dengue NS1 Antigen Rapid Test is a qualitative, lateral flow immunoassay for the detection of Dengue NS1 antigen in human serum, plasma, or whole blood. It is designed for the early diagnosis of dengue virus infection, especially during the first 1–7 days of symptom onset, enabling timely clinical intervention.

Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263.

Key Features

• Early Phase Detection: Identifies NS1 antigen, typically present in early dengue infection

• Fast Turnaround: Delivers results within 15–20 minutes

• Multi-Sample Compatibility: Works with serum, plasma, and whole blood

• Simple and Rapid Procedure: No laboratory equipment required

• High Diagnostic Accuracy: High sensitivity and specificity in clinical evaluations

• Field Ready: Ideal for use in hospitals, clinics, and mobile health units

• Individually Sealed Kits: For single-use, sterile testing and convenient storage
  
  

Industries Served

• Hospitals and Emergency Departments

• Clinical and Diagnostic Laboratories

• Tropical Disease Control Programs

• Mobile and Remote Health Camps

• Public Health and Epidemiological Surveillance

 

Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.

Product Details:

The Artus Hepatitis B Virus QS Kit is a real-time PCR-based diagnostic assay designed for the quantitative detection of Hepatitis B Virus (HBV) DNA in human plasma or serum. Manufactured to meet clinical diagnostic needs, this assay ensures high sensitivity and specificity for HBV DNA, supporting disease monitoring and antiviral therapy effectiveness in infected individuals. It is CE-IVD marked and optimized for use on various real-time PCR platforms, enabling efficient workflow integration in molecular diagnostic laboratories.

Note : The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263

Key Features

• Real-time PCR-based assay for quantitative HBV DNA detection
  
  

• High sensitivity and specificity with low detection limits
  
  

• CE-IVD certified for clinical diagnostic use
  
  

• Ready-to-use reagent system reduces handling errors
  
  

• Compatible with major real-time PCR instruments
  
  

• Enables viral load monitoring during and after therapy
  
  

• Includes internal control for process validation
  
  

Disclaimer

 

UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified.
MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.