Kit for specific detection of endometrial carcinoma
一种子宫内膜癌、试剂盒的技术,应用在生物测试、测量装置、材料检验品等方向,能够解决子宫壁薄弱、患者伤害、穿孔等问题,达到易保存、成本低、高应用价值的效果
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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 . 75 μg RNA library was reverse-screened through nitrocellulose membrane to remove membrane-bound RNA molecules, and then incubated with 2ug CYPA protein at 37°C for 30 minutes, the reaction solution was filtered through nitrocellulose membrane, and the filter membrane was washed; then the filter membrane was cut into pieces, Place in elution...
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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