Can the reagents be frozen and thawed multiple times?

Unused reagents can be cryopreserved but should not be thawed and frozen more than three times to avoid affecting stability.

What are the available specifications for the kit?

The kit is available in 32T/kit and 96T/kit specifications.

P105H UU Nucleic Acid PCR Detection Kit

Name: P105H UU Nucleic Acid PCR Detection Kit
Brand: Xi'an Tianlong Science and Technology Co., Ltd.
SKU: 1908894841

Shaanxi, ChinaXi'an Tianlong Science and Technology Co., Ltd.

Negotiable

1 Piece

Sample price:US$100.00/box.Request sample

Product profile

Customization

Available

Classification

Detection Kit

Type

Uu Nucleic Acid Detection Kitu

Model NO.

P105H

Certification

CE, FDA, ISO13485

Group

Middle-aged and Old

Spec

32T/kit, 96T/kit

Method

Fluorescence PCR Method

Brand

Tianlong

Validity

12 months.

Transport Package

Paper Carton with Icy Bag

Specification

44*44*45 cm

Trademark

Tianlong

Origin

China

HS Code

3822009000

Production Capacity

5000000 Test/Year

Key features

Fluorescence PCR Method: Utilizes specific primers and Taqman probes for accurate qualitative detection of Ureaplasma urealyticum.

Internal Control System: Synthetic non-competitive sequence monitors false negatives effectively in closed reaction systems.

Multiple Specification Options: Available in 32T/kit and 96T/kit formats to suit different laboratory needs.

Broad Instrument Compatibility: Compatible with ABI7500, TL988-IV, Gentier 96E/96R, and Gentier 48E real-time PCR systems.

Comprehensive Certifications: Holds CE, FDA, and ISO13485 certifications ensuring quality and regulatory compliance.

Flexible Customization: Offers full, minor, and flexible customization options from samples or designs.

Stable Storage and Transport: Valid for 12 months at -25 to -15 degrees Celsius with proven stability during transport.

OEM and ODM Services: Provides both OEM and ODM services with 111 R&D engineers supporting product development.

Company profile

Importers and ExportersHigh Repeat Buyers ChoiceExhibition ExperienceYears of Export Experience

Xi'an Tianlong Science and Technology Co., Ltd.

Shaanxi, China

Business Type: Manufacturer/Factory CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 20 years CertifiedNearest Port: Shenzhen Port, Shanghai PortAverage Response Time: ≤2.00h

AI-Powered supplier vetting

SummaryTianlong demonstrates established quality and management credentials, including ISO 13485, ISO 9001, ISO 14001, and ISO 45001:2018-related certifications. Its documented supplier-service procedures cover qualification assessment, corrective and preventive actions, and complaint handling, supported by 30 qualified service-capable suppliers. The supplier reports 10 production lines, 11–20 quality-control staff, 50 years of combined R&D-engineer experience, ODM and OEM capabilities, SDK availability, and recent new-product development. It supports extensive customization but does not provide 3D software design services. Inventory capability and participation in WHX Labs Dubai 2026 are indicated, while overseas agents or branches, overseas warehouses, and overseas showrooms are absent. Manufacturing subcontracting lacks a valid contract, and no factory environmental impact assessment report is available. Financial records are identified for 2023–2025, but the slices provide no performance values.

Supplier typeThe supplier is identified as a combined company with a business scope covering device sales, second-class medical device sales, instruments and meters, software and hardware, communications equipment, specialized chemicals excluding hazardous chemicals, and industrial automation systems. Its profile also covers manufacturing, export trade, service, quality control, R&D, and sustainability activities, indicating a diversified supplier rather than a narrowly specialized entity.

CertificationsThe supplier reports ISO 13485 and ISO 9001 certifications for supplier management systems, plus ISO 9001:2015, ISO 14001, and ISO 45001:2018-related sustainability certifications. These certifications explicitly support quality, medical-device management, environmental, and occupational-safety systems.

After-Sales capabilityThe supplier has written procedures and implementation records for complaint handling and corrective/preventive actions, and reports 30 qualified suppliers for service capability. It also has inventory capability and has participated in WHX Labs Dubai 2026, but it lacks overseas agents or branches, overseas warehouses, and overseas showrooms; therefore, the documented service processes are positive, while international service infrastructure is limited.

R&D capabilityThe supplier reports 50 years of total R&D-engineer experience, new products developed during the past year, ODM services, and an available SDK. These details provide explicit evidence of active R&D and product-development capability, although 3D software design services are not offered.

Production capacityThe supplier operates 10 production lines, has 11–20 quality-control staff, and reports in-stock service capability. However, the factory and related subcontractors do not have a valid manufacturing-capacity contract, which is a documented weakness in production governance.

Customization capabilityThe supplier offers customization from samples, customization from designs, full customization, minor customization, and flexible customization, and also provides ODM services. This indicates broad product adaptation and original-design support, despite the absence of 3D software design services.

Client casesThe supplier states that its products and services are available throughout the country, provides OEM services for well-known brands, and participated in the WHX Labs Dubai 2026 offline trade show. These are explicit market and customer-related references, but the slices do not identify specific customer names, projects, order histories, or performance outcomes.

Product Q&A

Q:What is the intended use of this kit?

The kit is used for qualitative detection of ureaplasma urealyticum nucleic acid in male urethral swab samples or female cervical swab samples.

Q:How should the reagents be stored?

All reagents should be stored at -25 to -15 degrees Celsius. The validity period is 12 months.

Q:What are the sample requirements?

Samples include male urethral swabs or female cervical swabs. They can be stored at 2-8 degrees Celsius for 24 hours, at -20 degrees Celsius for 3 months, or at -70 degrees Celsius for long-term storage.

Q:Which instruments are compatible with this kit?

It is suitable for ABI7500, TL988-IV, Gentier 96E, Gentier 96R, and Gentier 48E real-time PCR systems.

Q:What is the validity period of the reagents?

The validity period of the reagents is 12 months from the production date shown on the packaging label.