HPV/p16 Dynamic Range Analyte Control
Our HPV/p16 Analyte ControlDR
contains 4 cell lines that demonstrate a full Dynamic Range of expression for high risk human papilomavirus types 16 and 18: high, medium, low and negative. The same cell lines also demonstrate high homogenous, high heterogenous and negative expression of p16. Ideal for use as a same slide control for HPV in situ hybridization (ISH) and p16 immunohistochemistry (IHC) where maximum sensitivity is required. Available now, please contact firstname.lastname@example.org
or visit one of our distributors
[HCL001]: HPV/p16 Analyte ControlDR (2 unstained slides)
[HCL002]: HPV/p16 Analyte ControlDR (5 unstained slides)
[HCL003]: HPV/p16 Analyte ControlDR (1 cell microarray block)
Cell Line 1: High HPV ISH, p16 IHC heterogeneous positive
Cell Line 2: Medium HPV ISH, p16 IHC homogeneous positive
Cell Line 3: Low HPV ISH, p16 IHC homogeneous positive
Cell Line 4: Negative HPV ISH, negative p16 IHC
Human Papillomavirus or HPV is a group of more than 150 related viruses, over 40 of which can be transmitted through direct skin-to-skin contact during vaginal, anal and oral sex. High-risk HPV infection accounts for approximately 5% of all cancers globally. That said, most HPV infections occur without symptoms and regress within 2 years without causing cancer. Some HPV infections, however, persist and can progress to cancer if left untreated. HPV, through expression of E6 and E7, has a negative impact by binding to the p53 and retinoblastoma tumour suppressor pathways, and as such, integration of the virus typically leads to an overexpression of p16ink4A
Virtually all cases of cervical cancer are caused by HPV infection, with HPV 16 & 18 detected in 70%. HPV 16 is responsible for around 85% of anal cancers and HPV 16 & 18 account for approximately 50% of vaginal, vulval and penile cancers. Within the last 20 years, the incidence of HPV-associated oropharyngeal cancer has increased, particularly among men. HPV 16 has been identified in around 50% of oropharyngeal cancers in the US. Indeed it has been estimated that, by 2020, HPV will cause more oropharyngeal cancers than cervical cancers in the US.
HPV infection is determined using assays that detect viral DNA or RNA within the cell. p16 is commonly used as a surrogate marker of oncogenic HPV infection and can be demonstrated using immunohistochemistry (IHC). HPV DNA is most commonly assessed by polymerase chain reaction (PCR) and in situ hybridisation (ISH). Recently, more sensitive ISH assays able to detect HPV mRNA E6 & E7, have come into routine use. In determining the presence of HPV DNA/mRNA or p16 protein, the requirement of same slide controls are critical in the quality control of the results. Particularly in demonstrating adequate sensitivity of technically challenging assays such as ISH. The products from HistoCyte Laboratories have been developed for use as an analyte control for slide-based assays that suitably reflect the efficacy of the assays employed.