Rapid diagnosis reagent kit and detection method for cholera vibrio gene

A technology for rapid diagnosis of Vibrio cholerae, which is applied in biochemical equipment and methods, measurement/testing of microorganisms, resistance to vector-borne diseases, etc., to achieve high yield, low detection cost, and rapid amplification

Active Publication Date: 2011-08-10
GUANGZHOU HUAFENG BIOTECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Among them, isothermal amplification (Isothermal Amplification) nucleic acid rapid detection technology is a great progress in pathogenic nucleic acid detection technology, and the established loop-mediated isothermal amplification technology (loop-mediated isothermal amplification of DNA, LAMP) has many advantages. cholerae, and there is currently no gene rapid diagnostic kit for detection of Vibrio cholerae using loop-mediated isothermal amplification technology

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] (1) Synthesize oligodeoxynucleic acid primers by DNA synthesizer according to the following sequence:

[0036] Outer primer F3: GGTGACTTTATTGTGCGC;

[0037] Outer primer B3: GGCTACCTAACTCACCAC;

[0038] Internal primer FIP: ACTGCCAACTCACTTTGAGTGttttCCTCGGTAGTACCTAATGAC;

[0039] Internal primer BIP: CGCTTGGCTATATGTTTACTGACAttttCAGAGGTAGAAAATCTTATGTGAA;

[0040] (2) Purchase DNA polymerase: Bst DNApolymerase (large fragment) and place it in a container.

[0041](3) Preparation of reaction solution: The formula of the reaction solution contains 2mmol dNTP, 25mmol Tris-Cl, 12.5mmol potassium chloride, 12.5mmol ammonium sulfate, 10mmol magnesium sulfate, 1.25ml TritonX-100, 1mol betaine, 2 mol each of primers FIP / BIP and 0.25 mol each of outer primers F3 / B3 were prepared and placed in containers.

[0042] (4) Preparation of sample pretreatment solution: the formula of sample pretreatment solution was prepared by containing 20 mmol Tris-HCl (pH8.0), 2 mmol EDTA and 12 ml...

Embodiment 2

[0054] The formula of the reaction solution is: each 1L reaction solution contains 1.6mmol dNTP, 20mmol Tris-HCl, 10mmol potassium chloride, 10mmol ammonium sulfate, 8mmol magnesium sulfate, 1ml TritonX-100, 0.8mol betaine, internal primer FIP / BIP each 1.6 mol and 0.2mol each of outer primer F3 / B3;

[0055] The formula of the sample pretreatment solution is: every 1L of the sample pretreatment solution contains 10mmol of Tris-HCl with pH8.0, 1mmol of EDTA and 10ml of Triton X-100.

[0056] The chromogenic solution is EvaGreen.

[0057] Others are the same as embodiment 1.

[0058] Application of Example 3 Vibrio cholerae Gene Rapid Diagnostic Kit

Embodiment 3

[0059] 1. Sample processing (template DNA extraction)

[0060] (1) Take 25g (ml) of food samples by aseptic technique, and carry out bacterial enrichment treatment according to SN / T1022-2001;

[0061] (2) Take 1ml of the enrichment solution and centrifuge at 10000rpm for 2min to obtain bacterial sediment;

[0062] (3) Add 100 μl sample pretreatment solution to the above-mentioned bacterial cell precipitation and mix well, boil in boiling water for 10 minutes, immediately place on ice to cool for 10 minutes, centrifuge at 10,000 rpm for 2 minutes, and the supernatant is the sample template DNA.

[0063] 2. The reaction process of loop-mediated isothermal amplification technology

[0064] 1) Prepare a reaction system in a 200 μl reaction tube: 22 μl of reaction solution, 0.5 μl of Bst DNA polymerase (4U), 30 μl of stabilization solution, and 2.5 μl of template DNA.

[0065] 2) React the prepared reaction tube at a constant temperature of 64° C. for 1 h.

[0066] 3. Post-react...

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PUM

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Abstract

The invention discloses a rapid diagnosis kit and a detection method of genes of comma bacillus. The kit consists of two pairs of primers, DNA polymerase, stabilizing solution, reaction solution, sample pre-treatment solution, color development solution and positive comparison solution, wherein, the seven solutions are respectively placed in containers. The rapid diagnosis kit of genes of the invention applies six sections and four primers and can judge whether target materials exist only according to the amplification, thus being high in specificity. The rapid diagnosis kit of genes of the invention is high in speed, high in efficiency and sensitivity, can amplify the reaction with only constant temperature, without special reagents or equipment, and is low in detection cost. The rapid diagnosis kit of genes of the invention is simple and convenient in identification. Pyrophosphate ions separated out from the dNTP are combined with Mg<2+> in the reaction solution to produce a by-product which is the sediment of magnesium pyrophosphate which can be identified by naked eyes. Furthermore, after the color development solution is added, the color development differences of negative and positive results are notable and the identification is more obvious and reliable.

Description

technical field [0001] The invention relates to a biological detection reagent, in particular to a rapid diagnosis kit for Vibrio cholerae gene and a detection method thereof. Background technique [0002] At present, there are many detection methods for Vibrio cholerae, ranging from national standards (GB 15984-1995, SN / T1022-2001) focusing on the isolation and identification of pathogenic microorganisms, morphological identification and automatic biochemical identification, to immunological detection of specific proteins Technology, nucleic acid probe, polymerase chain reaction (PCR) technology and other molecular biology detection methods (SN / T 1872-2007). Among them, the detection of pathogenic nucleic acids has greatly improved in terms of rapidity, safety, accuracy and sensitivity. These new technologies try to break through the traditional microbiological detection modes such as morphology and biochemical reactions, and do not need to separate microorganisms. Purifi...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/68C12Q1/04
CPCY02A50/30
Inventor 曹以诚李志勇陈洵杜正平谭惠媚凌莉
Owner GUANGZHOU HUAFENG BIOTECH
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