Detection of streptococcus pneumoniae
A Streptococcus pneumoniae and probe technology, which is applied in the determination/testing of microorganisms, biochemical equipment and methods, etc., can solve the problem that there is no specific detection of Streptococcus genus
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Embodiment 1
[0090] Samples of blood culture positive for S. pneumoniae were obtained and DNA was extracted therefrom by means of the NucliSENSeasy MAG kit from BioMerieux. The initial volume of blood culture used was 1 ml and the final volume after elution was 80 μl.
[0091] Next, take an elution volume of 5 μl and amplify it with a mixture of the following reagents:
[0092]
[0093]
[0094] Amplification products were denatured by incubation at 95°C for 10 minutes. Afterwards, in the presence of a standard hybridization solution, 5 μl of the denatured PCR product was mixed with a protein containing SEQID immobilized at a known position. and SEQID Microarray incubation of probes.
[0095] After a series of standard washing and blocking steps, images were taken to obtain figure 1 A visualization of the final result is shown in .
Embodiment 2
[0097] Samples of blood cultures positive for S. light were obtained and the same procedure described in Example 1 was performed for S. pneumoniae. exist figure 2 A visualization of the final result is shown in .
Embodiment 3
[0099] Samples of blood cultures positive for oral Streptococcus were obtained and the same procedure described in Example 1 was performed for Streptococcus pneumoniae.
[0100] exist image 3 A visualization of the final result is shown in .
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