LAMP (loop-mediated isothermal amplification) detection kit of vibrio cholerae and detection method thereof
A technology for Vibrio cholerae and a detection method, applied in the biological field, can solve the problems of affecting PCR amplification results, difficult to meet rapid identification, expensive and the like, and achieve the effects of shortening reaction time, improving detection sensitivity, and shortening time-consuming
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Embodiment 1
[0043] Example 1: Preparation of immunomagnetic beads coupled with anti-Vibrio cholerae monoclonal antibody
[0044] Obtaining monoclonal antibody against Vibrio cholerae
[0045] The present invention can use the anti-Vibrio cholerae monoclonal antibody that has been disclosed in the prior art. In order to achieve a better detection effect, preferably, the present invention uses the cholera antibody secreted by the hybridoma cell line with the deposit number of CGMCC No.6754. Vibrio flagellin monoclonal antibody, the specific information and obtaining method of the monoclonal antibody have been described in detail in Chinese invention patent application 201210532294.3. In order to more fully disclose the above content, the present invention provides a specific acquisition method here:
[0046] 1. Cell culture and extraction of flagellin
[0047] Vibrio cholerae (Vibrio cholera) (VC-75, isolated and stored in the laboratory) was inoculated in T1N1 medium (purchased from Beij...
Embodiment 2
[0103] Embodiment 2: the composition of the LAMP detection kit of Vibrio cholerae
[0104] (1) Immunomagnetic beads coupled with anti-Vibrio cholerae monoclonal antibody; for example, the immunomagnetic beads prepared in Example 1;
[0105] (2) LAMP reaction solution, which includes the outer upstream primer (F3) shown in the sequence table SEQ ID No.1, the outer downstream primer (B3) shown in the sequence table SEQ ID No.2, and the sequence table SEQ ID No.3 The inner upstream primer (FIP) shown in the sequence table, the inner downstream primer (BIP) shown in SEQ ID No.4 in the sequence table, the circular upstream primer (LF) shown in SEQ ID No.5 in the sequence table, and the sequence table SEQ ID No. .6 The circular downstream primer (LB); said primers were all synthesized by Dalian Bao Biological Engineering Co., Ltd.;
[0106] Further, the LAMP reaction solution also includes ThermoPol buffer, dNTPs, betaine and MgSO 4 ; Wherein ThermoPol buffer, purchased from NEB C...
Embodiment 3
[0111] Embodiment 3: detect the specificity and sensitivity test of Vibrio cholerae kit
[0112] 1. Assay Specificity Analysis
[0113] The strains listed in Table 3 were detected by IMS-LAMP respectively, and the results showed that the amplified products of Vibrio cholerae standard strains were fluorescent green after staining with SYBR Green Ⅰ, and a typical ladder-shaped amplification band was detected by agarose gel electrophoresis ; while the rest of the strains had no specific amplification (see figure 1 ), without any false positive and false negative results, indicating that this method has good specificity for detecting Vibrio cholerae.
[0114] Table 3 list of experimental strains
[0115] serial number
strain name
serial number
1
Vibrio cholerae
isolate VC-75
2
ATCC1833
3
ATCC1758
4
Vibrio river
ATCC1.1611
5
Vibrio venice
ATCC1.1612 ...
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