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The CINtec PLUS Cytology Kit is an immunocytochemistry assay for the simultaneous qualitative detection of the p16INK4a and Ki-67 proteins in cervical cytology preparations. It is indicated to be used as an aid in the identification of women with high-grade cervical intraepithelial lesions in a screening population, and in the sub-groups of patients with a Pap cytology result of ASC-US (atypical squamous cells of undetermined significance) or LSIL (low-grade squamous intraepithelial lesion), or in patients with positive high-risk HPV test results.Interpretation of the test results may only be made by a certified professional in conjunction with the patient´s clinical history and additional diagnostic tests that have been performed.The product is intended for in vitro diagnostic (IVD) use.
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Hex Code
Color name
RGB
HSL
CMYK
#0B42CA
Denim
11, 66, 202
223, 90, 42
95, 67, 0, 21
#FFFFFF
White
255, 255, 255
0, 0, 100
0, 0, 0, 0
#006674
Mosque
0, 102, 116
187, 100, 23
100, 12, 0, 55
**CINtec® PLUS Cytology Kit** is an innovative immunocytochemistry assay designed for the simultaneous qualitative detection of p16INK4a and Ki-67 proteins in cervical cytology preparations. This product aids healthcare professionals in identifying women with high-grade cervical intraepithelial lesions, particularly in those with atypical Pap results or positive high-risk HPV test outcomes. The CINtec PLUS Cytology Kit employs dual-biomarker technology, enabling precise detection of transforming HPV infections.
By leveraging monoclonal antibodies for p16INK4a and Ki-67, combined with advanced detection systems, the kit offers objective and actionable results that facilitate timely follow-ups for affected individuals. Intended for in vitro diagnostic use, the product enhances the cervical cancer screening process, ensuring that women receive necessary and efficient care. The CINtec PLUS Cytology Kit exemplifies Roche Diagnostics' commitment to advancing cancer diagnostics, providing reliable tools for clinicians and better outcomes for patients.
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