Herpes simplex virus type 1 real-time fluorescent nucleic acid constant temperature amplification detection kit
A herpes simplex virus, constant temperature amplification detection technology, applied in the field of primers, probes and related kits, real-time fluorescent nucleic acid constant temperature amplification detection of herpes simplex virus type 1 (HSV-1), can solve the problem of inability to distinguish HSV infection Varicella-zoster virus infection, unable to distinguish between HSV-1 and HSV-2, unable to achieve rapid and quantitative detection, etc., to achieve high accuracy, accurate detection, and monitoring of the existence of false negatives
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Embodiment 1
[0097] Example 1 Design of special primers and probes for detection of herpes simplex virus type 1 (HSV-1) by real-time fluorescent nucleic acid constant temperature amplification
[0098] The present invention selects a highly conserved and specific segment in the HSV-1 US5 gene as the amplified target sequence region (its nucleotide sequence is shown in SEQ ID No.: 1), according to the principle of primer probe design, using DNAStar , DNAMAN software and artificially designed special primers and probe sequences for real-time fluorescent nucleic acid constant temperature amplification detection of herpes simplex virus type 1 (HSV-1), the following specific sequences are obtained:
[0099] (1) a capture probe (TCO, Target Capture Oligo) that can specifically combine with the target nucleic acid (HSV-1 RNA) sequence of herpes simplex virus type 1 (HSV-1), the nucleotide sequence of the capture probe is: 5' TGCACACCGGATGGCCAATCCAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 3' (SEQ ID No.: ...
Embodiment 2
[0108] Example 2 Preparation of a real-time fluorescent nucleic acid constant temperature amplification detection kit for herpes simplex virus type 1 (HSV-1)
[0109] Using the special primers and probes provided in Example 1, the real-time fluorescent nucleic acid constant temperature amplification detection kit for herpes simplex virus type 1 (HSV-1) of the present invention was obtained. The kit contains components such as capture probe (TCO, Target CaptureOligo), T7 primer, nT7 primer, HSV-1 detection probe, M-MLV reverse transcriptase and T7 RNA polymerase, among which:
[0110] The nucleotide sequence of the capture probe is SEQ ID NO: 2, the sequence of the T7 primer is SEQ ID NO: 3, the sequence of the nT7 primer is SEQ ID NO: 4, and the nucleotide sequence of the detection probe is SEQ ID NO: 5.
[0111]The capture probe is present in the viral nucleic acid extraction solution, the T7 primer, nT7 primer and HSV-1 detection probe are present in the HSV-1 amplification ...
Embodiment 3
[0127] Example 3 Specificity detection of the kit
[0128] The detection kit made by the present invention is similar to herpes simplex virus type 1 in classification, similar in symptoms, and prone to cross-reaction microorganisms for specific detection. Specifically, samples No. 1-9 are varicella-zoster virus (VZV), EB Virus (EBV), cytomegalovirus (CMV), simian herpes B virus, herpes simplex virus type 2 (HSV-2), human papillomavirus (HPV), Chlamydia trachomatis (CT), Neisseria gonorrhoeae bacteria (NG), Ureaplasma urealyticum (UU). The composition and specific method of the kit are as follows:
[0129] 1. Preparation of reference substance
[0130] 1.1 Internal standard: Take 400 μL of diluent, add 10 μL of HIV-1 internal standard (10 5 HSV-1 IC RNA dilution), mix well and set aside.
[0131] 1.2 Positive control: take 250 μL negative control, add 10 μL positive control substance (10 6 copy / mL dilution of herpes simplex virus type 1 in vitro transcribed RNA), mix well ...
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