Multiplex-polymerase chain reaction (PCR) detection method capable of simultaneously detecting vibrio parahaemolyticus, vibrio vulnificus and vibrio alginolyticus
A technology for Vibrio vulnificus and Vibrio alginolyticus, which is applied in the field of multiplex PCR detection, can solve the problems of long detection time, missed detection or false detection, missed detection, etc., and achieves simple method, short time consumption and reduced economic loss Effect
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Embodiment 1
[0030] a. With three standard strains of Vibrio parahaemolyticus Vibrio parahaemolyticus KCTC2471 , Vibrio parahaemolyticus L-0603121, Vibrio parahaemolyticus H040823-1 For the detected substance, the DNA template is prepared by the existing DNA extraction method and placed in the reaction tube;
[0031] b. Put Vibrio parahaemolyticus, Vibrio alginolyticus and Vibrio vulnificus primers into the reaction tube of step a to carry out multiple PCR reaction, the concentration of Vibrio parahaemolyticus primers is 1~20 pmol / μl, the Vibrio vulnificus The bacterial primer concentration is 1-20 pmol / μl, and the Vibrio alginolyticus primer concentration is 1-30 pmol / μl;
[0032] The primer sequence of Vibrio parahaemolyticus designed and synthesized according to the flaE gene of Vibrio parahaemolyticus is:
[0033] flaE-F:5'-GCAGCTGATCAAAACGTTGAGT-3'
[0034] flaE-R: 5'-ATTATCGATCGTGCCACTCAC-3'
[0035] The V. vulnificus primer sequence designed and synthesized according to the V...
Embodiment 2
[0045] The multiplex PCR reaction conditions and reaction system are the same as in Example 1, and the difference from Example 1 is that three strains of Vibrio alginolyticus are standard Vibrio alginolyticus KCCM40513 , Vibrio alginolyticus H050815-1s, Vibrio alginolyticus ATCC17749. for the detected substance.
[0046] Test results such as figure 2 as shown, figure 2 Middle M: DNA marker; 1: Negative control; 2-4: Amplified product of Vibrio alginolyticus. The results show that the method of Example 2 of the present invention can amplify the target band.
Embodiment 3
[0048] The multiplex PCR reaction conditions and reaction system are all the same as in Example 1, and the difference from Example 1 is that four strains of Vibrio vulnificus are standard Vibrio vulnificus ATCC29306, Vibrio vulnificus ATCC27562, Vibrio vulnificus ATCC2126, Vibrio vulnificus H0908272-C for the detected substance.
[0049] Test results such as image 3 as shown, image 3 Middle M: DNA marker; 1: Negative control; 2-5: Vibrio vulnificus amplification products. The results show that the method of Example 3 of the present invention can amplify the target band.
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