Salmonella and shigella joint detection kit and detection method thereof
A technology for Salmonella and Shigella, which is applied in biochemical equipment and methods, microbiological measurement/inspection, and resistance to vector-borne diseases. It can solve the problems of high missed detection rate, low missed detection rate, and long time consumption. Achieve high accuracy, high verification rate, and high yield
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Embodiment 1
[0065] Kit preparation
[0066] (1) Synthesize oligodeoxynucleic acid primers by DNA synthesizer according to the following sequence:
[0067] Salmonella
[0068] AgfA-9-F3: AGTTTCTGGCAGTGCTGTG (SEQ ID NO 1)
[0069] AgfA-9-B3: AGTACTGTTATCCGCACCCT (SEQ ID NO 2)
[0070] AgfA-9-FIP: ATCCGGGCCGGAACTATTGCTTTTCTGGCGTCGTTCCACAAT (SEQ ID NO 3)
[0071] AgfA-9-BIP: CGCTTGCTCTGCAAAGCGATGTTTTACCATAACCGCTCTGGGT (SEQ ID NO 4)
[0072] Shigella
[0073] ipaH-69-F3: ACATGAAGAGCAYGCCAACA Y represents C or T (SEQ ID NO 17)
[0074] ipaH-69-B3: TCCTCCAGCTCTCAGTGG (SEQ ID NO 18)
[0075] ipaH-69-FIP: CGGAATCCGGAGGTATTGCGTGTTTTCCTTTTCCGCGTTCCTTGA (SEQ ID NO 19)
[0076] ipaH-69-BIP: GGTCGCTGCATGGCTGGAAATTTTGCAGCAACAGCGAAAGACT (SEQ ID NO 20)
[0077] (2) Purchase DNA polymerase: Bst DNA polymerase is placed in the container;
[0078] (3) Prepare the buffer: the buffer is 0.18mol / L Tris-HCl, 0.10mol / L KCl, 0.07mol / L (NH 4 ) 2 SO 4 , 15mmol / L MgSO 4 , prepared with 1 volume % TritonX...
Embodiment 2
[0093] Kit preparation
[0094](1) Synthesize oligodeoxynucleic acid primers by DNA synthesizer according to the following sequence:
[0095] Salmonella
[0096] AgfA-56-F3: CCCGGATTCCACGTTGAG (SEQ ID NO 5)
[0097] AgfA-56-B3: TCGGAGTTTTTAGCGTTCCA (SEQ ID NO 6)
[0098] AgfA-56-FIP: CCGCTCTGGGTAATGGTCGTTTTTTTCTAACGCTGCGCTTGCTC (SEQ ID NO 7)
[0099] AgfA-56-BIP: ATGTAGGCCAGGGTGCGGATATTTTGGTCGATGGTGGCATTG (SEQ ID NO 8)
[0100] Shigella
[0101] ipaH-69-F3: ACATGAAGAGCAYGCCAACA Y represents C or T (SEQ ID NO 17)
[0102] ipaH-69-B3: TCCTCCAGCTCTCAGTGG (SEQ ID NO 18)
[0103] ipaH-69-FIP: CGGAATCCGGAGGTATTGCGTGTTTTCCTTTTCCGCGTTCCTTGA (SEQ ID NO 19)
[0104] ipaH-69-BIP: GGTCGCTGCATGGCTGGAAATTTTGCAGCAACAGCGAAAGACT (SEQ ID NO 20)
[0105] (2) Purchase DNA polymerase: Bst DNA polymerase is placed in the container;
[0106] (3) Prepare the buffer: the buffer is 0.25mol / L Tris-HCl, 0.15mol / L KCl, 0.15mol / L (NH 4 ) 2 SO 4 , 30mmol / L MgSO 4 , prepared with 2 volume % Trit...
Embodiment 3
[0116] Kit preparation
[0117] (1) Synthesize oligodeoxynucleic acid primers by DNA synthesizer according to the following sequence:
[0118] Salmonella
[0119] AgfA-19-F3: AGTTTCTGGCAGTGCTGTG (SEQ ID NO 9)
[0120] AgfA-19-B3: AGTACTGTTATCCGCACCCT (SEQ ID NO 10)
[0121] AgfA-19-FIP: ATCCGGGCCGGAACTATTGCCTGGCGTCGTTCCACAAT (SEQ ID NO 11)
[0122] AgfA-19-BIP: CGCTTGCTCTGCAAAGCGATG ACCATAACCGCTCTGGGT (SEQ ID NO 12)
[0123] Shigella
[0124] ipaH-69-F3: ACATGAAGAGCAYGCCAACA Y represents C or T (SEQ ID NO 17)
[0125] ipaH-69-B3: TCCTCCAGCTCTCAGTGG (SEQ ID NO 18)
[0126] ipaH-69-FIP: CGGAATCCGGAGGTATTGCGTGTTTTCCTTTTCCGCGTTCCTTGA (SEQ ID NO 19)
[0127] ipaH-69-BIP: GGTCGCTGCATGGCTGGAAATTTTGCAGCAACAGCGAAAGACT (SEQ ID NO 20)
[0128] (2) Purchase DNA polymerase: Bst DNA polymerase is placed in the container;
[0129] (3) Prepare the buffer: the buffer is 0.2mol / L Tris-HCl, 0.1mol / L KCl, 0.1mol / L (NH 4 ) 2 SO 4 , 20mmol / L MgSO 4 , prepared with 1 volume % TritonX-10...
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