Genotypus Papillomavirus Humani (XXVIII Typi)

Descriptio Brevis:

Hoc instrumentum ad detectionem qualitativam et genotypicam acidi nucleici 28 generum papillomavirus humani (HPV6, 11, 16, 18, 26, 31, 33, 35, 39, 40, 42, 43, 44, 45, 51, 52, 53, 54, 56, 58, 59, 61, 66, 68, 73, 81, 82, 83) in urina masculina/feminina et cellulis exfoliatis cervicis femineae adhibetur, media auxiliaria ad diagnosin et curationem infectionis HPV praebens.


Detalia Producti

Etiquettae Productarum

Nomen producti

HWTS-CC013-Instrumentum Detectionis Genotypi Virus Papilloma Humani (28 Typi) (PCR Fluorescens)

HWTS-CC016A-Instrumentum Detectionis Genotypi Papillomavirus Humani (28 Typi) Liquido Siccato (PCR Fluorescens)

Epidemiologia

Carcinoma cervicis uteri est unus e tumoribus malignis tractus genitalis feminini frequentissimis. Studia priora demonstraverunt infectionem persistentem et infectionem multiplicem papillomavirus humani unam e causis magnis cancri cervicis esse. In praesenti, adhuc desunt modi efficaces curationis HPV agniti, itaque detectio praecox et praeventio praecox HPV cervicis uteri sunt claves ad cancrum prohibendum. Methodum simplicem, specificam et celerem diagnosis aetiologicae constituere magni momenti est in diagnosi clinica cancri cervicis uteri.

Canalis

Buffer reactionis FAM VIC/HEX ROX CY5
HPV Genotyping Reaction Buffer 1 16 18 / Imperium internum
HPV Genotyping Reaction Buffer 2 56 / 31 Imperium internum
HPV Genotyping Reaction Buffer 3 58 33 66 35
HPV Genotyping Reaction Buffer 4 53 51 52 45
HPV Genotyping Reaction Buffer 5 73 59 39 68
HPV Genotyping Reaction Buffer 6 6 11 83 54
HPV Genotyping Reaction Buffer 7 26 44 61 81
HPV Genotyping Reaction Buffer 8 40 43 42 82

Parametri Technici

Repositorium Liquidum: ≤-18℃
Tempus conservationis Duodecim menses
Typus Speciminis Peniculus Cervicalis, Peniculus Vaginalis, Urina
Ct ≤28
CV ≤5.0%
Limitatio Detectionis (vel Limitatio Detectionis) 300 Exemplaria/mL
specificitas Omnia eventa negativa sunt cum apparatus adhibitus est ad detegenda specimina non specifica quae reactiones transversales cum eo habent, inter quae ureaplasma urealyticum, chlamydia trachomatis tractus genitalis, candida albicans, neisseria gonorrhoeae, trichomonas vaginalis, mucor, gardnerella et alia genera HPV quae ab apparatu non comprehenduntur.
Instrumenta Applicabilia Systema PCR Temporis Realis Applied Biosystems 7500

Systema PCR Temporis Realis Celeris Applied Biosystems 7500

QuantStudio®Quinque Systemata PCR Temporis Realis

Systema PCR Temporis Realis SLAN-96P

Cyclus Lucis®480 Systemata PCR Temporis Realis

Systema Detectionis PCR in Tempore Reali LineGene 9600 Plus

MA-6000 Cyclator Thermalis Quantitativus Temporis Realis

Systema PCR Temporis Realis BioRad CFX96

Systema PCR Temporis Realis BioRad CFX Opus 96

Fluxus Operis

Optio 1.

Reagentia extractionis commendata: Reagentium ad Exempla Macro et Micro-Test Liberanda (HWTS-3005-8)

Optio II.

Reagentia extractionis commendata: Instrumentum Macro & Micro-Test Viral DNA/RNA (HWTS-3004-32, HWTS-3004-48, HWTS-3004-96) et Extractor Automaticus Acidi Nucleici Macro & Micro-Test (HWTS-3006C, HWTS-3006B)


  • Praecedens:
  • Deinde:

  • Nuntium tuum hic scribe et nobis mitte.