Anoectochilus formosanus anthracnose LAMP detection primer and visible detection method thereof
A technology for detection primers and detection methods, which is applied in biochemical equipment and methods, recombinant DNA technology, and microbial determination/inspection, etc. Reliable results and highly sensitive results
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Embodiment 1
[0048] Example 1: Visual detection of LAMP primers for anthracnose of Clematis clematis
[0049] 1. LAMP Visual Detection of Clematis anthracnose
[0050] ①LAMP reaction system: 25μL reaction system containing 20mM Tris-HCl, 10mM (NH 4 ) 2 SO 4 , 10mMKCl, 8mM MgSO 4 , betaine 0.8mol / L, Bst DNA polymerase 8U, dNTPs 1.0mmol / L, F3 and B3 0.2mmol / L, FIP and BIP each 1.6mmol / L, calcein 50μmol / L, manganese chloride 500μmol / L, Tween-200.1%, template DNA50 ~100ng, make up the deficiency with sterile double distilled water; LAMP reaction conditions are incubation at 63-65°C for 45-60min, inactivation at 85°C for 5-10min.
[0051] ②After the LAMP reaction, green fluorescence was observed as a positive color, and orange was negative. Or take 2 μl of the amplification product and use 2% agarose gel electrophoresis to detect it. If the characteristic trapezoidal band of LAMP appears, it is judged as positive, and if no amplification band appears, it is judged as negative.
[005...
Embodiment 2
[0054] Example 2: Specific amplification of LAMP primers to Clematis anthracnose
[0055] 1. Specific detection of LAMP for anthracnose of Clematis aureus
[0056] ①LAMP reaction system: 25μl reaction system containing 20mM Tris-HCl, 10mM (NH 4 ) 2 SO 4 , 10mMKCl, 8mM MgSO 4 , betaine 0.8mol / L, Bst DNA polymerase 8U, dNTPs 1.0mmol / L, F3 and B3 0.2mmol / L, FIP and BIP each 1.6mmol / L, calcein 50μmol / L, manganese chloride 500μmol / L, Tween-200.1%, template DNA50 ~100ng, make up the deficiency with sterile double distilled water; LAMP reaction conditions are incubation at 63-65°C for 45-60min, inactivation at 85°C for 5-10min.
[0057] ②After the LAMP reaction, green fluorescence was observed as a positive color, and orange was negative. Or take 2 μl of the amplification product and use 2% agarose gel electrophoresis to detect it. If the characteristic trapezoidal band of LAMP appears, it is judged as positive, and if no amplification band appears, it is judged as negative...
Embodiment 3
[0060] Example 3: Sensitivity detection of LAMP primers to Clematis anthracnose
[0061] 1. Sensitivity detection of LAMP for anthracnose of Clematis aureus
[0062] Using the 10-fold concentration serial dilution method, the extracted DNA of Clematis anthracnose bacteria was diluted to 1000ng, 100ng, 10ng, 1ng, 100pg, 10pg, 1pg, 100fg, 10fg, 1fg, 100ag, 10ag, a total of 9 different concentration gradients.
[0063] ①LAMP reaction system: 25μl reaction system containing 20mM Tris-HCl, 10mM (NH 4 ) 2 SO 4 , 10mMKCl, 8mM MgSO 4 , betaine 0.8mol / L, Bst DNA polymerase 8U, dNTPs 1.0mmol / L, F3 and B3 0.2mmol / L, FIP and BIP each 1.6mmol / L, calcein 50μmol / L, manganese chloride 500μmol / L, Tween-200.1%, template DNA50 ~100ng, make up the deficiency with sterile double distilled water; LAMP reaction conditions are incubation at 63-65°C for 45-60min, inactivation at 85°C for 5-10min.
[0064] ②After the LAMP reaction, green fluorescence was observed as a positive color, and orange...
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