Anti-human papilloma virus L1 protein antibody, and coding gene and application thereof
An anti-human papilloma, L1 protein technology, applied in the field of anti-human papillomavirus L1 protein antibody and its coding gene, can solve the problem of uncontrolled proliferation of epithelial cells, and achieve high affinity, high affinity, and good specificity Effect
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Embodiment 1
[0034] Example 1 Screening of anti-human papillomavirus L1 protein single-chain antibody
[0035] The method disclosed in the Chinese patent literature with the publication number CN1444651A is used to construct a human single-chain antibody library, and to screen the anti-human papillomavirus L1 protein single-chain antibody in the human single-chain antibody library. The specific implementation process is as follows:
[0036] 1 Amplification of human antibody heavy chain and light chain variable region DNA
[0037] Using poly A+RNA (purchased from Clontech) from human bone marrow, human fetal liver, human spleen and human peripheral blood leukocytes as templates, using oligo (dT) and random primers (random primers), using reverse transcriptase kit (purchased from From Clontech), poly A+ RNA was reverse transcribed into cDNA according to the method guide provided with the Clontech kit.
[0038] Using the above cDNA as a template, use a series of primers that recognize the hu...
Embodiment 2
[0140] Example 2 Expression of recombinant human papillomavirus HPV16 type L1 protein and preparation of rabbit antiserum
[0141] The preparation of recombinant human papillomavirus HPV16 type L1 protein refers to Peng Qinglin et al. (Peng Qinglin, Zhang Ting, Fan Dongsheng, Zheng Wei, Xie Xixiu, Xu Yufei, Xu Xuemei (2009) "Expression and purification of HPV18L1 virus-like particles and preparation of guinea pig antiserum. "Basic Medicine and Clinical Practice, 29:1039-1043). Briefly: the HPV16 type L1 coding DNA fragment was adjusted according to the codon frequency of sf9 insect cells to optimize the codons of the HPV16 type L1 coding DNA, and the optimized coding DNA was inserted into the Xba I site of the pFastBac Dual vector to obtain the recombinant vector pFastBac- HPV16L1. Recombinant Bacmid was obtained by transforming Escherichia coli DH10Bac competent cells. Insect sf9 cells were transfected with recombinant Bacmid, cultured in a constant temperature incubator at...
Embodiment 3
[0144] Embodiment 3 specific detection
[0145] 1 Single-chain antibody expression and purification
[0146] The coding gene of the single-chain antibody #H16L1-A was cloned into the expression vector pET27b(+), and pET27b-H16L1a was constructed;
[0147] Transform pET27b-H16L1a into expression bacteria E.coli BL21(DE3), and induce expression with IPTG (0.5mM) according to the method provided by Novagen; in the expressed target protein, the N-terminal of scFv is the pelB sequence, which can be The expressed scFv is secreted into the periplasmic space of BL21(DE3); the C-terminus of the scFv contains an HSV tag and a 6×His tag to facilitate the purification of the target protein;
[0148] The method provided by Qiagen was conveniently separated and purified with Ni-NTA column to obtain the single-chain antibody against human papillomavirus HPV16 type L1 protein.
[0149] 2ELISA testing the specificity of single chain antibody to HPV16 type L1 protein
[0150] The HPV16 type ...
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