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1.
FIG. 2

FIG. 2. From: Development and Clinical Evaluation of a Highly Sensitive PCR-Reverse Hybridization Line Probe Assay for Detection and Identification of Anogenital Human Papillomavirus.

Alignment of 65-bp nucleotide sequences from the L1 regions of a total of 39 HPV genotypes. The target sequences for the SPF primers are boxed and flank the 22-bp interprimer region, as indicated. Positions are according to the HPV-16 sequence PPH16 (GenBank accession no. K02718).

Bernhard Kleter, et al. J Clin Microbiol. 1999 August;37(8):2508-2517.
2.
FIG. 1

FIG. 1. From: Development and Clinical Evaluation of a Highly Sensitive PCR-Reverse Hybridization Line Probe Assay for Detection and Identification of Anogenital Human Papillomavirus.

Schematic representation of the locations of the different general primer sets (MY 09/11, GP5+/6+, and SPF) on the HPV genome. The circular HPV DNA genome is represented by a single line, and boxes show the positions of the various early (E) and late (L) genes. Within the L1 region, the positions of the amplification targets as well as the expected amplimer sizes for each of the primer sets are indicated.

Bernhard Kleter, et al. J Clin Microbiol. 1999 August;37(8):2508-2517.
3.
FIG. 3

FIG. 3. From: Development and Clinical Evaluation of a Highly Sensitive PCR-Reverse Hybridization Line Probe Assay for Detection and Identification of Anogenital Human Papillomavirus.

Outline and representative examples of the INNO-LiPA HPV genotyping assay. The positions of the control line and the 28 specific probes for each of the 25 HPV genotypes are shown at the left. The number above each strip indicates the HPV genotype for which DNA was amplified by SPF primers. The precise interpretation of the hybridization patterns is described in detail in Materials and Methods.

Bernhard Kleter, et al. J Clin Microbiol. 1999 August;37(8):2508-2517.

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