Polynucleotide for inducing apoptosis and its coded polypeptide and use
A technology of polynucleotides and induced cells, which is applied in the fields of peptides, peptide antibodies, autoimmune diseases and tumor drugs, and can solve the problems of lymphocyte autoimmune diseases and immune active cell clearance obstacles, etc.
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Embodiment 1
[0087] Embodiment 1, two-step method flux quantification RT-PCR technique amplifies target gene
[0088] gene name
Upstream primer (5'-3')
Downstream primer (5'-3')
NIAG1
NIAG2
NIAG3
NIAG4
NIAG5
NIAG6
NIAG7
NIAG8
NIAG9
NIAG10
NIAG11
NIAG12
NIAG13
gtcgacgctgcttcgttg
tgtcgtgaggctgaggtgcag
cctcggttaaacactggtcgttc
tgtgtccgtcgccatgacag
acttcatcgtcatgcagagcgtc
ggaggtcgctgctatgatccg
cctcggttaaacactggtcgttc
tgtcccatgaggctgccc
cattgatgcacccattccagtg
atgccaggtcgttggaggt
gggtggccgaagcagaagac
gcaaccatcaatcccgtctcc
ctgagggaacgctaagtagtgtgtc
gcctcctggagtgtggtggtc
gtgaaacgtggttagtctcgtaaaatg
ttctgtcactcttactaggattcgcc
tggttgagtggcaggtgagg
ccgtcactccgtgtgcgc
gccttactggatcacacacagtttc
ttctgtcactcttactaggattcgcc
tccctaatagtagcgattcaggctc
tctccaggtctcggtgtagcg
gaggggggagctacaactcg
ggcagactctcaagatatt...
Embodiment 2
[0100] Embodiment 2, the construction of target gene eukaryotic expression vector
[0101] The purified product of secondary amplification and the eukaryotic expression vector pcDNA3.1 / V5-His-TOPO (Invitrogen, abbreviated as pcDT) were ligated according to the conditions suggested by the kit manufacturer. The ligation product was transformed into Escherichia coli DH5α by electric shock method, and the transformant was grown on a solid LB plate medium containing ampicillin, and the grown single clone colony was selected, the plasmid was extracted, digested with EcoRI, and the digested product was identified by agarose gel electrophoresis. Select positive clones with inserts, select the correct forward insert clones by sequencing (ABI PRISM 3700 DNA analyzer), and name them NIAG1, 2, 3, 4, 5, 6, 7, 8, 9, 10, respectively. 11, 12, 13.
[0102] At the same time, the culture fluid was collected, and the precipitated protein was analyzed by SDS-PAGE to obtain NIAG1, 2, 3, 4, 5, 6, ...
Embodiment 3
[0104] Example 3, Renilla luciferase reporter gene method to determine the effect of the target gene on inducing apoptosis
[0105] Co-transfect human embryonic kidney 293T cells with the target gene and pRL family Renilla luciferase reporter gene carrier, and detect the effect of the target gene on the cell state by detecting the activity of Renilla luciferase, such as cell number, cell survival rate, etc. . The genes whose Renilla luciferase activity was significantly reduced compared with the pcDT empty plasmid were screened out. The specific operation steps are as follows:
[0106] (1) Cell culture: 1.2×10 4293T cells (ATCC Number: CRL-11268) were plated on a 96-well cell culture plate (Costar, 3599) with DMEM (Dulbecco's modified Eagle's medium) medium (Hyclone, SH0022.02) containing 10% fetal bovine serum (100 μl medium / well), in 5% CO 2 , cultured in a cell culture incubator (SANYO, MCO-15AC) at 37°C for 24 hours.
[0107] (2) Prepare transfection working solution:...
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