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Wound Pathogen Panel(Fluorescence PCR Method) PR2028-WP01

  • A fast, accurate and economical Wound Pathogens & DR panel by rt-PCR.
  • Screening test for both 19 common Pathogens and 12 common Antibiotics Resistance Genes.
  • Premixed Lyphilized System.
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  • PR2028-WP01

  • BioTeke

Wound Pathogen Panel(Fluorescence PCR method)



wound pathogen panel





*Fluorescence PCR method.

*Screening and detection both of 19 common pathogens DNA and 12 common drug(antibiotics) resistance genes.

*Lyophilized reagents.



Validity: 12 Months

Model: PR2028-WP01

Specification: 8 Tests/Kit; 24 Tests/Kit








Intended Use

The kit is qualitative in vitro detection of 19 common pathogens DNA and 12 common drug(antibiotics) resistance(DR) genes from wound swab.

The pathogens and drug resistance genes detected are shown in the following [table 1].


[table 1]

Pathogen & DR gene type Species













Bacteria

Escherichia coli
Klebsiella aerogenes
Klebsiella oxytoca
Klebsiella pneumoniae
Citrobacter spp.1
Enterobacter cloacae
Acinetobacter baumannii
Proteus mirabilis
Pseudomonas aeruginosa
Serratia marcescens
Staphylococcus aureus
Staphylococcus saprophyticus
Streptococcus agalactiae
Enterococcus faecalis
Enterococcus faecium
Morganella morganii
Bacteroides fragilis
Staphylococcus epidermidis
Fungi Candida albicans









Drug resistance gene

blaKPC
blaNDM
blaVIM
blaIMP
blaOXA-48
mecA
vanA
vanB
CTX-M2
suL1
suL2
suL3

1. Include:Citrobacter freundii, Citrobacter werkmanii, Citrobacter portucalensis, Citrobacter youngae, Citrobacter cronae, Citrobacter braakii, Citrobacter arsenatis, Citrobacter amalonaticus, Citrobacter koseri.

2. Include:CTX-M 1 group, CTX-M 2 group, CTX-M 9 group.



Principle

The 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 from wound swab 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.



Operation Process

UTI kit operation process




Advantages

wound pathogen panel (2)

1. Multiple quantitative analysis

19 common pathogen nucleic acids and 12 common antibiotics resistance genes


2. Rapid response

With a fast PCR instrument, the test can be completed in 60 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




Storage Conditions and Shelf Life

  • Store at -20℃±5℃

  • Transport at room temperature(≤37℃) for no more than 1 month.

  • Valid for 12 months




Components

  • Wound lyophilized reagent 8*8 strip tubes/24*8 strip tubes.

  • Internal Control Dry powder *1 tube.

  • Internal Control solution 1mL*1 tube.

  • Wound Positive control 300uL*1 tube.

  • Wound Negative control 300uL*1 tube.

  • Dissolving solution 1mL*1 tube/1mL*3 tubes.


 

Specimens Requirements

1). Wound swab, collected samples from margin to margin in a 10-point zigzag fashion.

2). The samples should be used for detection within the same day or stored at 2-8℃ less than 7 days. Stored at <20℃ for 6 months, avoiding repeated freeze-thaw cycles.




Performance

1). Detection limitation: 200 CFU/mL.

2). Precision: (CV, %) of Ct ≤5%.

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

4). Specificity: Please refer to the User Manual.



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