Anti-aging secretory Klotho protein and coding gene thereof, recombinant expression vector and application
An expression vector, anti-aging technology, applied in the fields of application, genetic engineering, plant gene improvement, etc., can solve the problem of lack of protein processing mechanism
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Embodiment 1
[0047] Construction and expression of embodiment 1 recombinant prokaryotic expression vector
[0048] (1) Construction of recombinant expression vector
[0049] Design primers according to the known Klotho sequence number (Gen Bank.NC_000013) and optimization and BL21(DE3) vector cloning site:
[0050] Using the pcDNA3.1-Klotho constructed above as a template and using the following sequences (upstream and downstream primers) as primers, PCR amplification was performed to obtain PCR amplification products; then the PCR amplification products were double-digested with EcoRI and XhoI enzymes, Simultaneously, the pET-28a(+) plasmid was also double-digested synchronously, and the target fragment was recovered by electrophoresis (the size of the Klotho gene was 1764bp, figure 1 ) was purified by the PCR purification kit, and then ligated with the double-digested and purified pET-28a(+) vector (purchased from EMDBiosciences (Novagen)) by T4 DNA ligase to obtain pET-28a-Klotho. Whe...
Embodiment 2
[0058] Example 2 Expression, purification and identification of recombinant prokaryotic carrier protein
[0059] (1) SDS-PAGE analysis of expressed protein
[0060] After the bacterium collected in Example 1 was broken, the precipitate was collected by centrifugation, and the precipitate was washed with PBS buffer solution containing 2M urea, and the precipitate was collected by centrifugation at 17000g at 4°C for 30 min; Wash with PBS buffer, 4°C, 17000g, 30min centrifugation to collect the precipitate; then wash with PBS buffer 2 to 3 times, 4°C, 17000g, 30min centrifugation to collect the precipitate; finally dissolve the precipitate in PBS buffer, add the final concentration 1 mM DTT (dithiothreitol), stirred overnight at 4°C. Collect the supernatant by centrifugation at 4°C, 9000rpm, for 20min. Pack the column with NI-NTA filler, wash the column with pure water for 2-3 column volumes, and equilibrate the column with PBS buffer at pH 8.0. Stir the balanced filler and th...
Embodiment 3
[0063] Anti-aging activity detection of embodiment 3 recombinant Klotho protein
[0064] (1) Establishment of cell senescence model
[0065] Human immortalized skin keratinocytes (HaCaT) and human skin fibroblasts (HSF) were irradiated with medium-wave ultraviolet light, and the aging model of cell damage (the cells were purchased from Shanghai Aiyan and Shanghai Zhongqiao Xinzhu Biotechnology Co., Ltd., aging The model was established by UVB irradiation method): cell culture was carried out at 37°C, 5% (v / v) CO 2 Routine culture in the cell incubator, placed in different energy 700 ~ 1000mJ / cm 2 Irradiate under a UVB lamp, the distance between the lamp source and the culture bottle is 15cm, after the experimental group is irradiated, add PBS buffer solution to wash, then discard the PBS buffer solution, add 100μL culture solution (DMEM medium+10% (v / v) Newborn bovine serum), normal culture; after 24h, MTT method detects the growth inhibition rate of two groups of cells%=(1-...
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