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Chlamydia trachomatis Real Time 2.0, cod. AA842/50 - NEW -

New

Code AA842/50

KIT Name: Chlamydia trachomatis Real Time 2.0

Description: The product provides reagents necessary for the qualitative identification by Real Time PCR of the presence of Chlamydia trachomatis (CT) and simultaneous discrimination of serotype L (aetiological venereal linfogranuloma agent  - LGV) in both female and male human samples (urine, cervical swabs , urethral and ocular and seminal fluid). The used target regions are the 16S rRNA, the cryptic plasmid for the identification of the Swedish variant (nvCT) and the OMP1 gene for the serotype L. The kit contemplate the use of Uracil-N-glycosidase (UNG) to prevent contamination and false positive results and endogenous internal control. Positive Control is supplied in lyophilized form in the kit.

Platforms: RotorGene Q (Qiagen), CFX 96 (Biorad) or 7500 Fast (Applied Biosystem) - Janus PE Automatic Extractor 

Extraction: AA1001 - Manual (Column)
                   AA1318 - Automatic (Janus)
                   AA1185 - Automatic (MagCore)

Detection: Real Time PCR

Test: 50

 

 

Poster Chlamydia trachomatis Real Time 2.0 Download
Leaflet Chlamydia trachomatis Real Time 2.0 Download
VEQ 2018 Results Download
Copyright MAXXmarketing GmbH

 

Nuclear Laser Medicine srl
Viale delle Industrie, 3 - 20090
Settala (MI) - ITALIA
Tel: +39 02 952451 - Fax: +39 02 95245238/37

P.Iva/Cod.Fisc.: 08763060152 - Cap. Soc. € 110.000,00 i.v.

 

CERTIFIED QUALITY

Nuclear Laser Medicine srl is certified