Kit for specific detection of endometrial cancer
A technology of endometrial cancer and kits, applied in the direction of biological testing, measuring devices, material inspection products, etc., can solve problems such as perforation, weak uterine wall, patient injury, etc., and achieve high application value, easy storage, and low cost Effect
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Embodiment 1
[0018] Obtaining of embodiment 1 CYPA protein
[0019] The CYPA gene shown in Genbank: NP_066953 was expressed by the conventional eukaryotic expression method in the field, and the corresponding target polypeptide protein was obtained.
Embodiment 2
[0020] Screening and preparation of embodiment 2 nucleic acid aptamers
[0021] Design a random nucleic acid library containing about 20 nucleotides at both ends and 1 nucleotides in the middle as follows:
[0022] 5'-ATCGTCACCATGGATACATG(N39)TTGCACAATTGGACAGTTAC-3'; N39 represents 39 random nucleotides.
[0023] The single-stranded DNA library is amplified into double-stranded DNA, and the product is subjected to 2% agarose gel electrophoresis and then gel-cut to recover and purify; the recovered double-stranded DNA is used as a template to transcribe a single-stranded RNA random library in vitro, and the transcript is purified by PAGE . 75μg RNA library was reverse screened with nitrocellulose membrane to remove membrane-bound RNA molecules, then incubated with 2ugCYPA protein at 37°C for 30min, the reaction solution was filtered through nitrocellulose membrane, and the filter membrane was washed; then the filter membrane was cut into pieces and placed in Boil in elution b...
Embodiment 3
[0038] Example 3 The performance measurement of protein binding suitable gametes
[0039] Take 2.0 μg of aptamers, digest them with calf intestinal alkaline phosphatase (CIP) at 37°C for 1 hour, purify and recover the dephosphorylated RNA; label [γ-32P]ATP on the dephosphorylated RNA by T4 polynucleotide kinase end of RNA molecule. 10nmol of radioactively labeled aptamers were incubated with different concentrations (1-200nM) of CYPA at 37°C for 30min, and the reaction solution of each group was filtered through a nitrocellulose membrane, the filter membrane was washed, dried, and detected by a liquid scintillation counter. For the residual radioactivity, the same sample was measured twice in parallel. Calculate the dissociation constant between each aptamer and the target protein. The result is as follows:
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