Primer group, probe group and kit for synchronously detecting multiple pathogens related to genital tract infection
A technology for simultaneous detection of reproductive tract infection, applied in the field of primer compositions for pathogens and kits thereof, can solve the problems of low sensitivity, low sensitivity, and large impact on results, and achieves high reverse transcription efficiency, strong primer specificity, Check full effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0045] Example 1: Preparation of a multiplex fluorescent quantitative PCR kit for the detection of 15 reproductive tract pathogens
[0046] The multiplex fluorescent quantitative PCR amplification kit used in the detection of 15 kinds of reproductive tract pathogens of the present invention, the composition of the PCR amplification kit is shown in Table 1.
[0047] Table 1 Composition list of PCR amplification kit
[0048]
[0049] The kit of the present invention can be used to detect 15 kinds of reproductive tract pathogens: herpes simplex virus type 1 (HSV1), herpes simplex virus type 2 (HSV2), group B streptococcus (SAg), atopobium (AV), common Revobacterium (PV), Megasphaerum (ME), Motonia (MB), Neisseria gonorrhoeae (NG), Gardnerella (GV), Trichomonas vaginalis (TV), Treponema pallidum (TP) , Candida albicans (CA), Ureaplasma urealyticum (UU), Chlamydia trachomatis (CT), Mycoplasma hominis (MH) nucleic acid.
[0050] The design of 15 kinds of reproductive tract path...
Embodiment 2
[0075] Embodiment 2: the detection method of multiplex fluorescent quantitative PCR kit
[0076] 1. Detection kit
[0077] The multiplex fluorescent quantitative PCR kit prepared in Example 1 for the detection of 15 kinds of reproductive tract pathogens.
[0078] Detection object
[0079] 2.1 Preparation of internal standard granule normal saline containing housekeeping gene (hereinafter referred to as "internal standard normal saline"): Measure 800mL of normal saline (0.9% sodium chloride solution) into a 1000mL volumetric flask in the reference substance preparation room in the clean work area , adding 5.0×10 9 Copies / mL pathogen plasmid or particle 1mL, dilute to 1000mL with normal saline, turn over to mix well, so that the final concentration is 5.0×10 6 copies / mL. Transfer the above solution to a 1000mL beaker and divide it for use.
[0080] 2.2 7 samples to be tested were negative
[0081]Collect cervicovaginal secretion samples such as HPV16, HPV18, HPV51, ciliat...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com