• UTI
UTI-test-kit-2-_774_774
UTI-test-kit-2-_774_774
UTI-test-kit-800-800

Urinary Tract Infection (UTI) & DR Panel (Fluorescence PCR method)

A multiplex qPCR panel for detecting UTI-causing pathogens and key antimicrobial-resistance genes in a single run. Optimized for midstream urine samples, it enables rapid diagnosis, supports targeted therapy, and reduces inappropriate antibiotic use. Room-temperature-stable reagents ensure simple storage and transport.A multiplex Real-Time PCR kit designed for rapid detection of RSV, COVID-19, Influenza A/B, and other major respiratory pathogens. Includes internal controls, room-temperature-stable reagents, and compatibility with leading qPCR instruments. Ideal for clinical diagnostics, outbreak monitoring, and high-throughput testing.
UTI
  • Urinary Tract Infection (UTI) & Drug Resistance (DR) Gene Detection Kit is designed with specific primers and probes for different common pathogens and drug resistance genes. Polymerase chain reaction (qPCR) and multiple fluorescent probe technique are used to amplify and detect specific nucleic acid sequences of pathogens and drug resistance genes listed in Table 1. 
  • By adding edible yeast as internal control (IC), the extraction and detection process of pathogen nucleic acid in urine is monitored to effectively avoid false negative results. In order to avoid aerosol contamination of the amplified products, the UDG enzyme /dUTP system was added to the amplification system to effectively degrade the amplified products and avoid false positive results. 
  • This kit is a fully premix freeze-dried system. Taq enzyme, UDG enzyme, reaction buffer, specific primers and probes required for amplification are all lyophilized in PCR tubes. A total of 1-8 Wells are lyophilized powders for different target genes. Detection can be performed directly after adding dissolving solution and extracted nucleic acid.
  • Model: PR2026-UT01

  • Format: Test cassette

  • Storage: -25~-15℃(-13~-5℉)

  • Shelf life: 12 months

Components 8 samples/kit 24 samples/kit Ingredient
UTI Lyophilized Reagent 8×8 strip tubes 24×8 strip tubes Specific primer&probes for the detection of pathogens and DR genes in Table 1, dNTP/dUTP Mix, Mg2+, Taq polymerase and UDG enzyme
UTI Lysis Buffer 1 mL×1 tube 1 mL×3 tubes Surface active agent, balanced salt solution
Internal Control Dry Powder 1 tube 1 tube Edible yeast powder
Internal Control Solution 1 mL×1 tube 1 mL×1 tube Dnase/Rnase-free H2O
One Test Glass Beads 8 tubes 8 tubes×3 bags Glass beads
UTI Positive Control 300 μL×1 tube 300 μL×1 tube Plasmid containing every target gene sequence
UTI Negative Control 300 μL×1 tube 300 μL×1 tube Plasmid containing internal control sequence
UTI Dissolving Solution 1 mL×1 tube 1 mL×3 tubes Stabilizer

NOTE:

1. The kit can be transported at room temperature. (No more than 1 month)

2. The reagents repeated freezing and thawing should not exceed 7 times.

1. Multiple quantitative analysis

19 common pathogen nucleic acids and 12 common drug resistance genes

2. Rapid response

With a fast PCR instrument, the test can be completed in 30 minutes

3. Application scenarios

Urology routine testing/third-party testing laboratory/inspection department

Postoperative monitoring/disease control/scientific research units/doctors cooperate to publish articles

4. Product advantages

Freeze-dried system

Reduce transportation risks and increase stability

No extraction equipment required

1. Disposable powder free gloves & other personal protective equipments.

2. Pipettes (adjustable) & Sterile pipette tips.

3. Urine sample collection device.

4. 1.5 mL centrifuge tubes and racks.

5. Bench top centrifuge for centrifuge tubes and PCR tubes.

6. Vortex mixer(Power ≥40W).

7. Centrifuge tube holder for vortex mixer.

8. Metal bath/water bath (1.5mL centrifuge tube, 95℃).

9. Real-time PCR instrument with FAM/VIC/ROX/CY5 fluorescence channels (ABI7500, Bio-rad CFX96, QuantStudio, SLAN-96S, BTK-96).

1). Detection limitation: 200 CFU/mL

2). Precision: The coefficient of variaation (CV, %) of Ct value of within-batch/between-batch precision is ≤5%

3). Accuracy: The conformity rate of negative/positive reference: 100%

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