Urinary Tract Infection Molecular Testing Kit

UTI KIT

The UTI comprehensive kit detects, by Molecular Technique, urinary pathogens. Our testing is completed with high sensitivity and specificity compared to the traditional urine culture technique. We identify pathogens that are difficult to grow in a culture while using the largest pathogen menu available.

COLLECTION & TESTING PROCESS

  • Estimate the quantity of normal vaginal flora and compare with pathogenic species
  • Detect ten pathogenic species causing bacterial vaginosis
  • Provide the results in text and graphical format
  • Provide suggestive treatment of BV based on the results
  • Monitor the efficacy of antimicrobial therapy
  • Can detect Aerobic vaginitis, candidiasis

ACCURACY AND QUICK RESULTS

Now your lab can provide healthcare providers with the quickest and most accurate results possible to allow them to determine an accurate diagnosis:

  • Expedited patient results
  • Drug resistance marker results available prior to antibiotic sensitivity results
  • Traditional antibiotic sensitivity results accompany UTI results
  • Individual pathogen test ordering available
  • Direct access to experience scientific staff
  • Personal customer service experience

For Research Use Only. Not for use In diagnostic procedures.

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DTPM, Inc. is a nationwide provider of laboratory products, services, and solutions. DTPM has partnered with laboratories since 1993 to provide a comprehensive array of instrumentation, custom assays, laboratory consumables, supplies, and ongoing service and support.

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Pathogens Detected in the DTPM UTI Molecular Testing Kit:

Pathogen Strain(s) Identified* Target Gene GenBank Accession Number Amplicon1 (base pairs) BLAST Score2 Range (High/Low) Sequences3 Reviewed Matches4 (True Positives) Specificity5
Candida albicans Candida albicans, Candid dubliniensis Erg11 NC_032093 74 142/134 1.02E+08 363 100%
Candida parapsilosis Candida parapsilosis Erg11 NW_023503279 65 130/130 1.02E+08 502 100%
Candida tropicalis Candida tropicalis Erg11 NW_003020060 70 140/134 1.02E+08 369 100%
Enterobacter cloacae/hormaechei Enterobacter cloacae, E. hormaechei, E. roggenkampii, E. asburiae, E. ludwigii, E. kobei, E. bugandensis apbC NZ_CP009756 72 138/133 1.02E+08 748 100%
Enterococcus faecalis E faecalis recG NZ_CP091198 66 132/122 1.02E+08 619 100%
Escherichia coli / Shigella Escherichia coli, O55H7, O157:H7, O10:H32, O104:H4, O121:H19, O178:H19, O6:H16, O169:H41, O25:H16, O27:H7, O128:H27, O114:H49, O15:H11, O6:H16, O127:H6, O4:H5, 025:H1, O8:H28, O170:H18, 085:H1, 0158:H24. Shigellla boydii, S. flexneri, S. dysenteriae lacY NC_000913 75 147/137 1.02E+08 4629 100%
Klebsiella oxytoca Klebsiella oxytoca, K grimontii, K michiganensis, Raoultella terrigena TonB NZ_CP033844 60 117/112 1.02E+08 179 100%
Klebsiella pneumoniae Klebsiella variicola, Klebsiella quasipneumoniae, Klebsiella africana gyrA NC_016845 57 114/105 1.02E+08 3138 100%
Klebsiella pneumoniae Klebsiella pneumoniae, K variicola, K quasipneumoniae, K africana gyrA NC_016845 57 114/107 1.02E+08 3189 100%
Morganella moranii Morganella moranii gyrA CP014026 65 130/120 1.02E+08 63 100%
Mycoplasma hominis Micoplasma hominis, Metamycoplasma hominis KtrB CP009652 79 158/153 1.02E+08 21 100%
Nakaseomyces glabratus [previously Candida glabrata] Nakaseomyces glabratus previously known as Candida glabrata Erg11 NC_006028 64 128/128 1.02E+08 101 100%
Proteus mirabilis Proteus mirabilis gyrA NC_010554.1 61 122 1.02E+08 143 100%
Providencia stuartii Providencia stuartii RecA/RadA CP003488 64 128 1.02E+08 20 100%
Psuedomonas aeruginosa Psuedomonas aeruginosa, P. alcaligenes, P. balearica, P. citronellolis, P. furukawaii, P. fluorescens, P. guangdongensis, P. jinjuensis, P. knackmussii, P. lalkuanensis, P. multiresinivorans, P. nitroreducens, P. otitidis, P. oryzihabitans, P. stutzeri, P. tohonis, P. paraeruginosa, Stutzerimonas balearica, S. frequens, S. stutzeri oprL NC_002516.2 60 120/90 1.02E+08 2035 100%
Serratia spp V2.0 Serratia marescens, S. bockelmannii, S. entomophila, S. ficaria, S. grimesii, S. liquefaciens, S. nematodiphila, S. odorifera, S. plymuthica,S. proteamaculans, S. quinivorans, S. surfactantfaciens, S. symbiotica, S. ureilytica, S rubidaea gyrA NZ_CP027798 66 120/109 1.02E+08 1333 100%
Staphylococcus aureus Staphylococcus aureus acetyl-CoA acetyltransferase NC_007795 59 112/107 1.02E+08 1912 100%
Staphylococcus aureus Staphylococcus aureus acetyl-CoA-acetyltransferase NC_007795 59 112/104 1.02E+08 1969 100%
Staphylococcus saprophyticus Staphylococcus saprophyticus KtrB NZ_CP014113 66 132 1.02E+08 25 100%
Streptococcus agalactiae Streptococcus agalactiae gyrA CP003919 72 141/136 1.02E+08 216 100%
Ureaplasma urealyticum Ureaplasma urealyticum ureC NC_011374 75 150 1.02E+08 8 100%
Footnotes:

  1. The Amplicon is the amplified piece of DNA which contains the Fwd, Rev and Probe sequence. Sequence between the Fwd, Rev and Probe are also included in Amplicon.
  2. The BLAST Score describes how similar the Amplicon sequence is to aligned sequences in the non-redundant GenBank Database. The range shown as High/Low reflects the highest and lowest scores for a pathogen that would generate a positive response using this assay.
  3. The number of sequences reviewed reflect the total number sequences in the non-redundant GenBank database on the date of the analysis. This number will change as new sequences are added to the GenBank database.
  4. Matches reflect the total number of pathogens identified in the BLAST search that would generate a positive ressponse. Statistically these are the number of True Positives (the diagnostic test would indicates the presence of the correct disease) = TP
  5. False positive (FP) – Test incorrectly detects the presence of pathogen in a sample that does not contain the pathogen. Shown as an incorrect pathogen in the BLAST analysis with a Score within the High/Low range listed for the assay.
    True negative (TN) – Test correctly identifies absence of pathogen. Calculated from BLAST data as the (total number of sequences reviewed) – (total number of pathogens correctly detected or TP).

Specificity = TN / TN + FP
https://lexjansen.com/nesug/nesug10/hl/hl07.pdf

* If you have inquiries about specific strains, please contact DTPM support.

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