Aptamer C201 of staphylococcal enterotoxin C2 as well as screening method and application of aptamer C201
A technology of staphylococcus intestine and nucleic acid aptamer, which is applied in pharmaceutical formulations, biochemical equipment and methods, and medical preparations containing active ingredients, etc., can solve the problems of high reagent cost, poor adsorption selection specificity, etc. Good properties, small molecular weight and good permeability
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Embodiment 1
[0047] Example 1: Screening of nucleic acid aptamer C201
[0048] The screening method of the nucleic acid aptamer C201 of the Staphylococcus aureus enterotoxin C2, it comprises the following steps:
[0049] (1) Preparation of the screening library: design a random ssDNA library (5'-AGGGCCGAGCTCACTTGT-N 35 -CCGCCGGCACAATTGTGC-3'), and commissioned Sangon Bioengineering Co., Ltd. to synthesize.
[0050] (2) Coupling of Staphylococcus aureus enterotoxin C2 with carboxyl magnetic beads: the Staphylococcus aureus enterotoxin C2 protein was purchased from Toxin Technology Company of the United States, and the carboxyl magnetic beads and their coupling reagents were purchased from Bangs Laboratories Company of the United States. The operation refers to the instructions provided by the manufacturer; the change of the protein concentration in the Staphylococcus aureus enterotoxin C2 solution before and after coupling is measured by the BCA method for protein concentration, and the co...
Embodiment 2
[0058] Example 2: Analysis of the nucleic acid aptamer C201 sequence:
[0059] (1) After 9 rounds of screening, the enriched ssDNA library was collected, and Shanghai Passino Biotechnology Co., Ltd. was entrusted to use high-throughput sequencing technology to analyze the library sequence. The analysis process was: PCR amplification of the enriched library, And add the sequencing adapter and Index part; select and purify the library by gel electrophoresis; use the Agilent 2100Bioanalyzer to control the quality of the library through the Agilent High Sensitivity DNA Kit; use the Quant-iT PicogGreen dsDNAAssay Kit to quantify the library; use the IlluminateNextSeq 500 platform to single The chain library is used as a template for bridge PCR amplification, sequencing primer annealing, and sequencing while synthesizing; and performing comparison and enrichment analysis on the sequencing results.
[0060] (2) Using the UNAFold network platform to analyze at 25°C, 100mM Na + , 1 mM...
Embodiment 3
[0061] Example 3: Specificity analysis of the nucleic acid aptamer C201:
[0062] (1) FAM-labeled nucleic acid aptamer C201 was chemically synthesized in vitro and dissolved in selection buffer.
[0063] (2) Referring to step (2) in Example 1, BSA, Staphylococcus aureus enterotoxin A, Staphylococcus aureus enterotoxin B and Staphylococcus aureus enterotoxin C1 were respectively coupled with carboxyl magnetic beads to prepare BSA magnetic beads , Staphylococcus aureus enterotoxin A magnetic beads, Staphylococcus aureus enterotoxin B magnetic beads, Staphylococcus aureus enterotoxin C1 magnetic beads and Staphylococcus aureus enterotoxin C2 magnetic beads. Wherein, the BSA was purchased from Sigma Company, and the Staphylococcus aureus enterotoxin A, Staphylococcus aureus enterotoxin B and Staphylococcus aureus enterotoxin C1 were all purchased from Toxin Technology Company of the United States.
[0064] (3) Take 200 μL of the nucleic acid aptamer C201 solution obtained in step...
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