Human epididymis expression sperm binding protein HEL-90, encoding gene and application thereof
A HEL-90 and protein-binding technology, applied in the fields of biotechnology and medicine, can solve the problems of poorly understood protein functions and achieve the effect of less side effects
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Embodiment 1
[0039] Example 1. Preparation of human epididymis expression protein HEL-90 by genetic engineering technology
[0040] Gene cloning and sequence analysis
[0041] Large-scale sequencing and screening of the human epididymis cDNA library constructed in our laboratory was performed to obtain expressed sequence tags (EST), and electronic cloning was performed using the Unigene database to obtain the full-length cDNA of human HEL-90. Using Expasy Translate tool (http: / / us.expasy.orghttp: / / us.expasy.org), InterProScan (http: / / www.ebi.ac.uk / Tools / http: / / www.ebi.ac. uk / Tools / ) and Protein roteinblast (http: / / www.ncbi.nlm.nih.gov / BLAST / http: / / www.ncbi.nlm.nih.gov / BLAST / ) etc. to predict the peptide sequence of HEL-90 and assumed functions. SignalP (http: / / www.cbs.dtu.dkhttp: / / www.cbs.dtu.dk), PSORTII and WoLFPSORT (http: / / psort.nibb.ac.jp) and other software analyzes and predicts the signal peptide of the protein and intracellular localization. ProfileScan (http: / / myhits.isb-sib.c...
Embodiment 2
[0045] Example 2. Preparation of anti-HEL-90 polyclonal antiserum
[0046] Polyclonal antibodies were prepared by immunizing BALB / C mice with recombinant HEL-90 protein. Briefly, each mouse was injected with 50 μg of recombinant protein and the same amount of complete Freund's adjuvant (CFA) on day 1. Then on the 15th, 30th and 45th days, 25 μg of recombinant protein and the same amount of incomplete Freund's adjuvant (IFA) were injected to boost the immunization. On the 60th day, blood was collected from the eyeball, and the serum was separated to analyze the titer and specificity of the antibody by ELASA and western blot. ELISA analysis showed that the antibody titer reached 1:10000. Western blot showed good specificity for both recombinant protein and native HEL-90 extracted from human epididymis fluid.
Embodiment 3
[0047] Example 3. Study on tissue expression profile of human HEL-90mRNA
[0048] In order to determine the expression pattern of HEL-90, semi-quantitative RT-PCR was used to analyze the expression difference of HEL-90 gene in human epididymis head, body, tail, testis, heart, liver, spleen, lung, kidney, stomach and other tissues. Use TRIzol (Tiangen, Beijing, China) to extract total RNA, 1ug total RNA uses 20UAMV reverse transcriptase (Promega) and 0.3ugoligod T 18 (Promega) was reverse transcribed into cDNA. Then, 2ul of the synthesized cDNA was amplified by PCR using gene-specific primers. 20ul reaction system contains: 2ul 10×PCR buffer (with MgCl 2 ), 2ul dNTP Mix (10mmol / L), 1ul each primer ul (25umol / L), 1ul Taq DNA polymerase (2.5U / ul), 2ulcDNA template and 11ulddH 2 O. The program of PCR reaction was: 94°C, 10min; 94°C, 1min; 54°C (for HEL-90) / 49°C (β-actin) for 30s; 72°C, 1min (35 cycles); 72°C extension for 7min. The expression of βactin was used as an intern...
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