Dermatophyte PCR kit The Dermatophyte PCR Kit is a multiplex PCR system that enables determination of dermatophytes generally and T. rubrum from nail samples within 5 hours. General Nail infections are caused chiefly by T. rubrum and T. mentagrophytes. Traditionally, these species are identified from nail samples by culturing on medium, which takes 1015 days to 34 weeks. The Dermatophyte PCR Kit is a multiplex PCR system that enables determination of dermatophytes generally and T. rubrum from nail samples within 5 hours. The primer mix contains two primer pairs aimed at, respectively, chitin synthase 1 for detection of dermatophytes generally and ITS2 (internal transcribed spacer) to detect T. rubrum. Furthermore, the primer mix contains an internal plasmid control that functions as a template for the primer pair specifically for T. rubrum. By comparing the dermatophyte multiplex PCR method with conventional methods of identifying nail infections, it has been shown that the PCR method identifies most dermatophyte and T. rubrumpositive nail samples (ref. 1, 2 and 3). Product description The kit contains all reagents necessary to carry out dermatophyte PCR reactions. The kit contains Buffer A and Buffer B to prepare the template, primer mix and PCR Ready Mix (including loading buffer) to run the samples and two PCRpositive DNA controls—one containing dermatophyte genomic DNA and one containing T. rubrum genomic DNA. There is enough reagent for 100 PCR reactions in the kit. Use The Dermatophyte PCR Kit is used for in vitro diagnostics of dermatophytes in general and T. rubrum from nail samples. Product range Article number Product Number of tests Packing 73411 Dermatophyte PCRkit 100 1 box References 1. A. BrillowskaDabrowska, D. M. Saunte and Maiken Cavling Arendrup. Fivehour diagnosis of dermatophyte nail infection with specific detection of Trichophyton rubrum. Jour Clin Microbiol (2007) 12001204. 2. N. Kondori, A.L. Abrahomsson, N. Ataollahy and C. Wennerås. Comparison of a new commercial test, DermatophytePCR kit, with conventional methods for rapid detection and identification of Trichophyton rubrum in nail specimens. Medical Mycology (2010), Early Online, 14. 3. A. BrillowskaDabrowska, S. S. Nielsen, H. V. Nielsen and M. C. Arendrup. Optimized 5hour multiplex PCR test for the detection of tinea unguium: performance in a routine PCR laboratory. Medical Mycology 2010, 48, 828 831 4. Nisha Suyien Chandran, JiunYit Pan,Zacharias AD Pramono, HiokHee Tan and ChewSwee. Complementary role of a polymerase chain reaction test in the diagnosis of onychomycosis. Australasian Journal of Dermatology (2013) 54, 105–108 Downloads Brochures Dermatophyte PCR Kit Packaging inserts Dermatophyte PCR kit Material safety data sheets Dermatophyte PCR kit Declarations of Conformity DoC Dermatophyte PCR Webshop Find the product in our webshop SHOP.SSIDIAGNOSTICA.COM Printed from www.ssidiagnostica.com on 14.06.2017, 13:43 © Statens Serum Institut 2017 This page can be found at: Frontpage Products PCR Dermatophyte PCR kit SSI Diagnostica A/S 2 Herredsvejen 3400 Hillerød T +45 4829 9100 F +45 4829 9179 EAN 5790 002327452 E [email protected] Sitemap
© Copyright 2026 Paperzz