Prostate lesion tissue immunofluorescence detection kit and detection method

By adopting abiotic amplification system and multiple rounds of labeling technology in the prostate lesion tissue immunofluorescence detection kit, the problems of antibody species limitation and long experimental cycle in the existing technology are solved, and rapid and strong signal multiple labeling detection is achieved, which is suitable for the diagnosis of lesions such as prostate cancer.

CN119335186BActive Publication Date: 2025-03-21HUNAN AIFANG BIOTECHNOLOGY CO LTD
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Patent Information

Application Number
CN202411884716.2
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2024-12-20
Publication Date
2025-03-21
Estimated Expiration
2044-12-20

AI Technical Summary

Technical Problem

During the detection of the existing immunohistochemistry double staining kit for prostate lesions, the use of ready-to-use combination antibodies, resulting in different types of antibodies. Rabbit monoclonal antibodies with strong specificity and strong affinity cannot be used at the same time, and it is easy to cause circulating staining, and the experimental cycle is long.

Method used

Using abiotic amplification system, combined with TYR-xxxPlus fluorescent dye and TSA Buffer, HRP-labeled secondary antibodies catalyze the activation of tyramine fluorescein substrate in the presence of hydrogen peroxide, to achieve fluorescent signal amplification, and triple labeling is achieved through multiple rounds of labeling technology to avoid interference from endogenous biotin.

Benefits of technology

It greatly shortens the experimental time, enhances the intensity of fluorescence signal, avoids circulating staining and endogenous biotin interference, and is suitable for the diagnosis and differential diagnosis of prostate cancer, PIN, and AAH.

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Abstract

The present invention proposes a prostate lesion tissue immunofluorescence detection kit and detection method, which belong to the technical field of kits. It is prepared from the following raw materials by weight: 40-60 parts of TYR-xxxPlus fluorescent dye, 30-45 parts of TSA Buffer, 20-40 parts of Polymer-HRP monoclonal antibody mouse / rabbit secondary antibody, 15-30 parts of antibody, 5-15 parts of Dapi dye solution, 50-70 parts of antibody diluent, and 50-70 parts of peroxidase blocking solution. This kit adopts a non-biotin amplification system, which greatly shortens the experimental time compared with traditional double staining experiments and effectively avoids the interference of endogenous biotin. It is suitable for the diagnosis and differential diagnosis of prostate cancer, PIN, and AAH in prostate resection specimens, needle biopsy specimens, electroresection specimens, and transurethral resection specimens, and is particularly suitable for conventional formalin-fixed paraffin-embedded sections.
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