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Hepatitis C virus (HCV) fluorescent PCR detection kit

NegotiableUpdate on 05/06
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Overview

The hepatitis C virus (HCV) fluorescence PCR detection kit is designed with specific primers and probes for the conserved region of the HCV genome. One step fluorescence RT-PCR technology is used for in vitro amplification and detection of HCV RNA, which is used for pathogen detection of suspected infectious materials in scientific research experiments.

Product Details

Product Name: Hepatitis C Virus (HCV) Fluorescent PCR Detection Kit

Name : Hepatitis C virus Detection Kit(Real-Time PCR Method)

【 Packaging Specification 】 50T/box

Hepatitis C is an infectious disease mainly caused by liver damage due to infection with hepatitis C virus (HCV), and belongs to Class B infectious disease. This kit is suitable for detecting the RNA of hepatitis C virus in patient serum and plasma samples, and is suitable for auxiliary diagnosis of hepatitis C virus infection.

【 Principle of Inspection 】

This kit is designed with specific primers and probes for the conserved region of the hepatitis C virus genome. One step fluorescent RT-PCR technology is used for in vitro amplification and detection of hepatitis C virus RNA, which is used for pathogen detection of suspected infectious materials in scientific research experiments.

【 Reagent Composition 】

Packaging Specifications 50T/box
HCV reaction solution 500 μ L x 2 tubes
Enzyme solution 50 μ L x 1 tube
HCV positive quality control product 50 μ L x 1 tube
Negative quality control product 250 μ L x 1 tube







Explanation: Components of different batch numbers of reagent kits cannot be used interchangeably.

Storage conditions and expiration date

-20 ℃± 5 ℃, stored in the dark, transported, and subjected to repeated freeze-thaw cycles no more than 5 times, with a validity period of 12 months.

ABI7500、 Agilent MX3000P/3005P, LightCycler, Bio Rad, Eppendorf and other series of fluorescence quantitative PCR detectors.

Serum: Use a disposable syringe to extract 2 mL of venous blood from the subject, place it in a sterilized disposable non anticoagulant test tube with a unique identification number, and directly use the separated serum for testing, storage, or submission. Plasma: Use a disposable syringe to extract 2 mL of venous blood from the subject, place it in a sterilized disposable anticoagulant (non heparin) test tube with a unique identification number, and directly use the separated plasma for testing, storage, or submission. Hemolytic samples should be re sampled. If the triglyceride content exceeds 6 mmol/L or if the plasma or serum appears white and turbid to the naked eye, the sample should be centrifuged at 4 ℃ 16200g for 15 minutes and the clear serum or plasma from the lower layer should be aspirated.

[Storage and Transportation]

The collected or processed samples should be stored at 2 ℃~8 ℃ for no more than 24 hours; if long-term storage is required, they should be stored at -70 ℃ or below, with no more than 3 freeze-thaw cycles.

【 Precautions 】

1.All operations must be strictly carried out in accordance with the instructions;

2.Before use, all components in the reagent kit should be naturally melted, thoroughly mixed, and briefly centrifuged;

3.The reaction solution should be stored away from light;

4.Try to avoid the presence of bubbles during the reaction, and cover the tube tightly;

5.Use disposable suction tips, disposable gloves, and specialized work clothes for each area;

6.Sample processing, reagent preparation, and sample addition should be carried out in different areas to avoid cross contamination;

7.After the experiment is completed, treat the workbench and pipette with 10% hypochlorous acid, 75% alcohol, or a UV lamp;

8.All items in the reagent kit should be treated as contaminants and handled in accordance with the "Biosafety Guidelines for Microbial Biomedical Laboratories".

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