Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3

Customization: Available
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Products Details

  • Overview
  • Product Description
  • Detailed Photos
  • Company Profile
  • Our Advantages
  • Certifications
  • FAQ
  • Packaging & Shipping
Overview

Basic Info.

Model NO.
RM-FP-069
Content
Standard
Usage
Laboratory Reagents, Analytical Reagents, Diagnostic Reagents
Habit Appellation
Second Kind of Reagent
Application
Scientific Research, Health
Property
Biochemical Reagent
Product Name
Hpv DNA Nucleic Acid Detection Kit
Sample
Available
Color
Transparent
Appearance
Liquid
MOQ
20 Test
Brand
Runmei
Storage
-20
Package
Box
Certificate
ISO MSDS CE
Transport Package
Cold Chain
Specification
50 test
Trademark
RUNMEI
Origin
Hunan, China
HS Code
3822190090
Production Capacity
5000boxes Per Month

Product Description

 
Human Papilloma Virus Genotyping Detection Kit HPV DNA Detection Kit
(Fluorescence PCR Method)

Product Description

This kit is used for the detection of human papilloma virus Nucleic Acid(HPV type 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68). Specific types of HPV 16, 18 and 45 can be identified in one reaction tube and 14 HPV viruses can be tested in parallel in another reaction tube.The kit also assisted diagnosis and epidemiological surveillance of Human Papilloma Virus(HPV). For professional in vitro diagnostic use only.

 
KIT CONTENTS
Number Composition 20 Tests/Kit 50 Tests/Kit 200 Tests/Kit
1 11+3-A-HPV PCR Reaction Solution 300uL*1 tube 750uL*1 tube 750uL*4 tubes
2 11+3-B-HPV PCR Reaction Solution 300uL*1 tube 750uL*1 tube 750uL*4 tubes
3 HPV Enzyme Mixture 200uL*1 tube 500uL*1 tube 500uL*4 tubes
4 HPV Negative Control 100uL*1 tube 100uL*1 tube 100uL*4 tubes
5 HPV Positive Control 100uL*1 tube 100uL*1 tube 100uL*4 tubes
6 Instructions 1 serving 1 serving 1 serving

Test Principle
This kit is based on the principle of fluorescent PCR technology, designed specific primers and Taqman probes for Human Papilloma Virus, and detect them with a fluorescent PCR instrument to achieve detection of Human Papilloma Virus nucleic acids. 11+3-A-HPV PCR Reaction Solution detection type 16 (FAM channel) ,type 18 (HEX channel) and type 45(ROX channel). 11+3-B-HPV PCR Reaction Solution detectionl HPV 31, 33, 35, 39, 51, 52, 56, 58, 59, 66, 68  in paralle (FAM channel).
In addition, the PCR detection system contains internal control primers and probes to monitor the sample collection and the extraction process by detecting whether the internal standard is normal, to avoid false negative results.

 
Product Operation
Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3
Storage Conditions and Expiring Date
• The kit should be stored at -20 ± 5C. Validity 12 months.
• The production date and the expiration date stated on the outer packaging .
• Avoid repeated thawing and freezing more than 5 times . Please use the reagents within 1 month after opening.

Applicable Instrument
This kit is suitable for ABI series, Bio-Rad series, Agilent Stratagene MX series, Roche LightCycler R480, Cepheid SmartCycler, Rotor-Gene series and other multi-channel real-time quantitative PCR instruments.

Detailed Photos

Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3

 

Company Profile

Hangzhou Beiwo Medical Technology Co., Ltd.

      Beiwo was founded in 2018 and headquartered in Hangzhou, China with sister company, Biomiga Inc. located in San Diego, USA. Beiwo is based in the fields of molecular biology and diagnostics, and has a unique "product + service" model. Beiwo's partners include UWI, Genescript,Peking University, Tsinghua University, Zhejiang University, UCSD and other well-known institutions.
      Beiwo has a R&D team consisting of experts from wordwide, and has established a high-standard 100,000-grade GMP production workshop and obtained the ISO9001 quality management system certification.
      Based on the business philosophy of "trust comes from quality". Beiwo Medical focuses on global needs and is dedicated to providing customers with quality products and good technical services.

Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3

Our Advantages

Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3

Certifications

Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3

FAQ

Q: What kinds of products do you have?
A: sample preparation and purification, analysis and detection, BEIWO has corresponding reagents, instruments and even automation platform for scientific research institutions, academic institutions and industrial customers in the biopharmaceutical industry.

Q: How can I get the sample to check your quality?
A: We can ship the sample by international express like FEDEX, DHL etc, or we can choose the appropriate express logistics for you according to your requirements. Sample and freight cost will be needed.

Q: Can you provide different specifications of the kits according to the quantity we need?
A: Yes, we can provide the kits according your requirements, and we also can do ODM and OEM.

Q: What's your MOQ?
A: The MOQ for kits is 10 boxes. If some samples are needed, the total number of samples cannot be less than 5 boxes. For customized products, you can set the scales with your specification, logo, packing, etc, so the MOQ shall be negotiated.

Q: Do you have any certificates?
A: Yes, we have the certificatesISO9001, CErequired for export and local import custom clearance.

Q: What's your production capacity?
A: We have the production capacity of 50 thousand tests of kits per month.

Q: What's your lead time?
A: Our lead time is 5-10 days, if you need a large amount, the lead time may be 7-15 days, if more, then the exact time can be negotiated.

Q: What are your method of payment?
A: We support L/C, D/P, or T/T to business account.

Packaging & Shipping

Real Time PCR Human Papilloma Virus Genotyping Hpv Detection Kit 11+3

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