Application of vdac protein in inhibition of cell growth by sodium oxalate or calcium chloride
A technology of sodium oxalate and calcium chloride, which is applied in antibacterial drugs, chemical instruments and methods, and resistance to media-borne diseases, can solve the problems of timely and accurate earthquake prediction, and achieve the goal of preventing and mitigating natural disasters Effect
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Embodiment 1
[0028] Example 1 Detection of the inhibition rate of 7 peptides to Escherichia coli MG1655
[0029] Each synthetic peptide was dissolved in sterile water so that the stock solution concentration of the peptide was 20 mM. Then, each peptide was diluted to four final concentrations with four corresponding liquid media to form peptide solutions, which were 40 μM, 80 μM, 160 μM, and 320 μM, respectively. Dilute Escherichia coli to 4*10 5 cfu / ml final concentration. According to Table 2, the bacterial solution and the peptide solution were spotted on a 96-well plate, and three parallel controls were set for each spotting well. According to the culture time of Escherichia coli previously determined, put the 96-well plate with the sample in the incubator at 37°C for 20 hours and measure the OD value at 492nm with a microplate reader. According to the measured OD value, the antibacterial rate of various peptides against Escherichia coli in different concentrations and different med...
Embodiment 2
[0035] Example 2 Detection of the inhibition rate of 8 kinds of peptides to Saccharomyces cerevisiae INVSc1
[0036] Each synthetic peptide was dissolved in sterile water so that the stock solution concentration of the peptide was 20 mM. Then, each peptide was diluted to four final concentrations with four corresponding liquid media to form peptide solutions, which were 40 μM, 80 μM, 160 μM, and 320 μM, respectively. Dilute Saccharomyces cerevisiae to 1*10 3 cfu / ml final concentration. According to Table 3, the bacterial solution and the peptide solution were spotted on a 96-well plate, and three parallel controls were set for each spotting well. According to the previously determined yeast culture time, place the 96-well plate with the sample in a 30°C incubator for 21 hours and measure the OD value at 492nm with a microplate reader. According to the measured OD value, the bacteriostatic rate of various peptides against yeast in different concentrations and different media...
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