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37results about How to "Short sequence length" patented technology

Expression Vectors Containing a Truncated Epstein Barr Nuclear Antigen 1 Lacking the Gly-Gly-Ala Domain for Enhanced Transient Gene Expression

This invention relates to the unexpected discovery that nucleotide coding sequences coding for a truncated Epstein Barr Nuclear Antigen 1 (EBNA1t) protein (lacking the Gly-Gly-Ala domain), when in cells of mammalian origin, are associated with improved growth and increased transient gene expression when compared with cells expressing a complete EBNA1 coding sequence. The expression of EBNA1t also appear to be more stable over time.
Owner:NAT RES COUNCIL OF CANADA

Method for preparing aromatic-aliphatic copolyester

InactiveCN101412804APromote degradationDegradability hasDiolCopolyester
The invention relates to a method for preparing aromatic-aliphatic copolyester. In the method, aromatic binary acid, dihydric alcohol and aliphatic hydroxy acid are used as a copolymerization system to prepare the aromatic-aliphatic copolyester by direct melt polycondensation under the action of a catalyst, wherein the dihydric alcohol is one or both of aliphatic dihydric alcohol and cyclized aliphatic dihydric alcohol. The method overcomes the defect of the generation of poisonous methanol in the prior ester exchange process. By the random copolymerization, a polylactic acid chain segment can be introduced to an aromatic polyester chain segment, and the sequence length of an aromatic component is reduced, thereby improving the degradation property of the copolyester and keeping better mechanical behavior; moreover, the method also has the advantages of simple synthesis process, easy reaction operation and low-priced and easily obtained materials, and the obtained copolyester has certain degradation property.
Owner:NINGBO INST OF TECH ZHEJIANG UNIV ZHEJIANG

Method for automatically detecting similarity level of audio signals and system of method

The invention discloses a method for automatically detecting the similarity level of audio signals and a system of the method. The method includes the steps that the two segments of audio signals to be detected are obtained; frequency-domain analysis is performed on the audio signals, and all frequency-domain energy local peak value positions are found; frequency-domain energy local peak values are connected to form a pitch trail; according to the frequency-domain energy local peak value positions, a significant value of each audio frame is calculated, and an average significant value is obtained; according to the average significant value, a threshold value of phonic part judgment on the pitch trail is calculated; the part, exceeding the threshold value, of the average significant value is removed to obtain main melody sequences of the two segments of audio signals; a similarity matrix of two main melodies is obtained; a dynamic planning local warping algorithm is applied to binarization processing, so that a binary matrix is obtained; then the similarity level of the two segments of input audio signals is judged. By the adoption of the method or the system, detection efficiency is improved for the similarity level of the audio signals, the problem of plagiarism in audio spread is solved, and accurate and comprehensive protection is provided for right management of digital audios.
Owner:FUDAN UNIV

Nucleic acid aptamer capable of detecting myohemoglobin, microfluidic chip for screening and screening method and application

The invention discloses a nucleic acid aptamer capable of detecting myohemoglobin and a derivative of the nucleic acid aptamer. The nucleotide sequence of the nucleic acid aptamer comprises a DNA segment shown by any one sequence in the sequences from sequence 1-sequence 5 shown in the description. The invention discloses a microfluidic chip which comprises a sample inlet, a sample outlet and a sample feeding channel. The sample feeding channel is divided by two narrow channels into front, middle and rear channels. The front channel is filled with reverse screening protein modified microspheres, and the middle channel is filled with positive screening protein modified microspheres, wherein the grain size of microspheres is greater than width of the narrow channels. The invention further discloses a screening method for screening the nucleic acid aptamer by using the microfluidic chip. The method comprises the main steps of optimizing a nucleic acid library, screening initially, purifying, and circulating. The detection method provided by the invention has the advantages of high affinity and specificity.
Owner:HUNAN UNIV

Synthesis of degradable aromatic/fatty copolymer ester by in-situ ester

InactiveCN1817939AImprove hydrolytic degradation performanceShort sequence lengthSolventPolyester
Synthesis of degradable aromatic / fatty copolymer ester by low lactic acid in situ ester exchange is carried out by mixing AAC and DO with D, L-PLA in proportion of 1:1: (0-1.0), copoly-condensing without solvent or with diphenyl ether as solvent and synthesizing the final product.
Owner:江西省飓风化工有限公司

uPAR (urokinase-type plasminogen activator receptor) targeted peptides, probe and living molecular imaging method

The invention discloses uPAR (urokinase-type plasminogen activator receptor) targeted peptides with the amino acid sequence indicated in SEQ ID NO. 1. The uPAR targeted peptides is linear peptides formed by 13 amino acids, the peptides are easy to synthesize and can form a stable conformation and be combined with uPARs with specific target. The invention discloses a uPAR targeted probe comprisinga single unit and the above uPAR targeted peptides. The uPAR targeted probe is subjected to specific identification of the peptides and is combined with the uPARs, signals for detection of imaging equipment are transmitted through the signal unit, living visual detection of the uPARs is achieved, and distribution and number of the uPARs are displayed visually and are used for disease detection foruPAR expression abnormalities. The invention further discloses a living molecular imaging method. The uPAR targeted probe is utilized, and the living molecular imaging method has the advantages of being safe, non-invasive, dynamic, visual and the like and is suitable for direct detection of human body.
Owner:HUAZHONG NORMAL UNIV

Beta hairpin antibacterial peptide with tryptophan and arginine cross-chain interaction and preparation method of beta hairpin antibacterial peptide

The invention provides a beta hairpin antibacterial peptide with tryptophan and arginine cross-chain interaction and a preparation method of the beta hairpin antibacterial peptide. The sequence of theantibacterial peptide WRLPG is shown as SEQ ID No. 1. The preparation method comprises the following step: designing an antibacterial peptide template XWYRYPGXWYRY-NH2 containing tryptophan and arginine cross-chain interaction and a PG corner unit on the basis of beta-hairpin amphiphilic peptide arrangement, wherein X= R, and Y= L. The invention also provides application of the antibacterial peptide in preparation of medicines for treating infectious diseases caused by gram-positive bacteria or / and gram-negative bacteria. The antibacterial peptide forms a stable beta-hairpin structure under the condition that a disulfide bond formed by cysteine pairs is not contained, the length of an amino acid sequence is only 12, the antibacterial peptide has excellent biosecurity on the basis of maintaining high antibacterial activity, and the treatment index reaches 90.78. The antibacterial peptide has high development potential of replacing antibiotics.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Expression vectors containing a truncated epstein barr nuclear antigen 1 lacking the Gly-Gly-Ala domain for enhanced transient gene expression

This invention relates to the unexpected discovery that nucleotide coding sequences coding for a truncated Epstein Barr Nuclear Antigen 1 (EBNA1t) protein (lacking the Gly-Gly-Ala domain), when in cells of mammalian origin, are associated with improved growth and increased transient gene expression when compared with cells expressing a complete EBNA1 coding sequence. The expression of EBNA1t also appear to be more stable over time.
Owner:NAT RES COUNCIL OF CANADA

Method for optimizing pilot frequency sequence based on observation matrix in uplink SCMA system

The invention discloses a method for optimizing a pilot frequency sequence based on an observation matrix in an uplink SCMA system, and relates to a method for optimizing the pilot frequency sequencebased on the observation matrix. The method aims to solve the problems of high pilot cost, low detection precision and complex reconstruction of the existing method in sparse channel detection. The method comprises the following steps: 1, establishing an observation matrix model consisting of pilot sequences; 2, setting the pilot frequency set size of the registered user as N, and setting the signal-to-noise ratio threshold value as [gamma]; if the SNR of the receiving end is less than or equal to [gamma], executing step 3; if the receiving end SNR is greater than [gamma], executing the step 4; 3, calculating a block sparse observation matrix formed by a pilot frequency sequence set in the observation matrix model; and 4, calculating a block sparse observation matrix formed by the pilot frequency sequence set in the observation matrix model. The method is applied to the field of pilot frequency design of SCMA.
Owner:HARBIN INST OF TECH

Single-stranded DNA aptamer specifically recognizing tobramycin and application thereof

The invention discloses a single-stranded DNA aptamer specifically recognizing tobramycin and application thereof, and belongs to the technical field of biology. On the basis of ap32-34nt, by removingsome of terminal base pairs and unpaired bases and shortening the stem region length of a secondary structure, a tobramycin aptamer ap32-15nt with the greatly shortened sequence length and the improved affinity is obtained; the aptamer ap32-15nt is applied to construction of various tobramycin detection methods and detection reagents; the aptamer has the advantages of high affinity, high specificity, a stable structure and the like; and the constructed detection methods have the advantages of a short detection period, high sensitivity, low cost, strong specificity and the like.
Owner:JIANGNAN UNIV

Antibacterial peptide YHX-3 and composition and application thereof

The invention belongs to the technical field of biology, and particularly relates to an antibacterial peptide YHX-3 and a composition and application thereof, and an amino acid sequence of the antibacterial peptide YHX-3 is as shown in SEQ ID No.1. The antibacterial peptide YHX-3 provided by the invention has broad-spectrum antibacterial activity, and has remarkable antibacterial activity on gram-positive bacteria and gram-negative bacteria including listeria monocytogenes, staphylococcus aureus, streptococcus mutans, escherichia coli and salmonella; and the antibacterial peptide has low hemolytic activity, a small sequence length, low molecular weight, and low chemical synthesis difficulty, and reduces large-scale production cost very well while killing pathogenic bacteria in organisms more specifically,.
Owner:OCEAN UNIV OF CHINA

Isothermal amplification system and method based on fluorescence self-inhibition probe

The invention provides an isothermal amplification system and method of a fluorescence self-inhibition probe. The isothermal amplification system comprises a combination of two fluorescence self-inhibition probes, a Vent DNA polymerase, an Nt.BstNBI nicking endonuclease, a buffer solution, a reaction raw material and miRNA target molecules. The fluorescence self-inhibition probes comprise a fluorescence self-inhibition linear probe and a fluorescence self-inhibition hairpin probe. The invention also provides an amplification method of the isothermal amplification system. According to the fluorescence self-inhibition probe isothermal amplification system and the amplification method, background fluorescence signals of the probe can be remarkably reduced, the detection signal-to-noise ratio is greatly increased, and detection of trace miRNA targets in a sample is facilitated. Meanwhile, no complementary sequence exists between the two background-free fluorescent probes, mismatching and extension between the probes can be prevented, the detection specificity is effectively improved, false positive results are avoided, and the system and method are particularly suitable for direct detection of miRNA molecular markers in clinical samples.
Owner:HEFEI INSTITUTES OF PHYSICAL SCIENCE - CHINESE ACAD OF SCI +1

Method and kit for identifying six types of perciform fishes and raw meat products thereof based on DNA Barcoding

The invention discloses a method for identifying six perciform fishes and raw meat products thereof based on DNA Barcoding. The method comprises the following steps: (1) designing a synthetic primer according to the known fish DNA Barcoding database; (2) extracting various fish DNAs containing the six fishes, performing PCR amplification by the primer, and selecting the best primer and the reaction condition according to the amplified result; (3) performing amplification on the DNA of each to-be-tested sample by using the primer screened by the step (2), sequencing, correcting and comparing the amplified fragment to obtain the DNA Barcoding databases of various fishes; (4) detecting a new to-be-tested sample by using the primer screened by the step (2), comparing with the sequence length in the DNA Barcoding database of the step (3), and determining whether the to-be-tested sample is one of the six types of perciform fishes. The method provided by the invention is low in cost, simple and convenient in operation and high in accuracy; the identification for the six types of perciform fishes and the raw meat products thereof can be realized and a technical support for carrying out the works such as the food safety supervision and management and the species and environment protection can be provided.
Owner:GANSU AGRI UNIV

Blood group antibody detection method and application thereof

ActiveCN114113639ASolve the problem that cannot be expressed in full lengthShort sequence lengthDisease diagnosisBiological testingBlood group antibodiesAmino acid
The invention provides a blood group antibody detection method, a blood group antibody detection kit, a blood group antibody binding protein, nucleic acid for coding the blood group antibody binding protein and a carrier containing the nucleic acid. Particularly, the blood group antibody binding protein comprises more than 80% of homology with SEQ ID NO: 2, 4, 6, 8 or 10 or comprises an amino acid sequence shown as SEQ ID NO: 2, 4, 6, 8 or 10, has antigen specificity, and can be used for blood group antibody detection.
Owner:BEIJING DAYOU TIANHONG TECH CO LTD

Lightweight time convolution network for quick prediction of time series data

The invention discloses a lightweight time convolution network for quick prediction of time series data. An overall thought framework and a specific structure of the lightweight time convolution network are improved, expansion convolution is replaced by one-dimensional step convolution, and a full convolution structure is removed; as the calculated amount of the lightweight time convolution network provided by the invention is greatly reduced, and all calculation results in the overall thought framework of the lightweight time convolution network are used in forward and backward propagation ofthe network, the calculation waste is reduced; and meanwhile, compared with the prior art, the calculated amount required by the network is also greatly reduced; and meanwhile, the depth of the network can be effectively reduced by using a relatively large convolution kernel and a relatively large convolution step length.
Owner:BEIHANG UNIV

Method of generating a signal for distance measurement and method and system for distance measurement between a transmitter and a receiver

For generating a signal for distance measurement between a transmitter and a receiver, a sequence of pulses with predetermined respectively different time intervals between individual pulses is generated.
Owner:FRAUNHOFER GESELLSCHAFT ZUR FOERDERUNG DER ANGEWANDTEN FORSCHUNG EV

Nucleic acid aptamer capable of detecting myohemoglobin, microfluidic chip for screening and screening method and application

The invention discloses a nucleic acid aptamer capable of detecting myohemoglobin and a derivative of the nucleic acid aptamer. The nucleotide sequence of the nucleic acid aptamer comprises a DNA segment shown by any one sequence in the sequences from sequence 1-sequence 5 shown in the description. The invention discloses a microfluidic chip which comprises a sample inlet, a sample outlet and a sample feeding channel. The sample feeding channel is divided by two narrow channels into front, middle and rear channels. The front channel is filled with reverse screening protein modified microspheres, and the middle channel is filled with positive screening protein modified microspheres, wherein the grain size of microspheres is greater than width of the narrow channels. The invention further discloses a screening method for screening the nucleic acid aptamer by using the microfluidic chip. The method comprises the main steps of optimizing a nucleic acid library, screening initially, purifying, and circulating. The detection method provided by the invention has the advantages of high affinity and specificity.
Owner:HUNAN UNIV

Method for preparing aromatic-aliphatic copolyester

InactiveCN101412804BPromote degradationDegradability hasCopolyesterDiol
The invention relates to a method for preparing aromatic-aliphatic copolyester. In the method, aromatic binary acid, dihydric alcohol and aliphatic hydroxy acid are used as a copolymerization system to prepare the aromatic-aliphatic copolyester by direct melt polycondensation under the action of a catalyst, wherein the dihydric alcohol is one or both of aliphatic dihydric alcohol and cyclized aliphatic dihydric alcohol. The method overcomes the defect of the generation of poisonous methanol in the prior ester exchange process. By the random copolymerization, a polylactic acid chain segment can be introduced to an aromatic polyester chain segment, and the sequence length of an aromatic component is reduced, thereby improving the degradation property of the copolyester and keeping better mechanical behavior; moreover, the method also has the advantages of simple synthesis process, easy reaction operation and low-priced and easily obtained materials, and the obtained copolyester has certain degradation property.
Owner:NINGBO INST OF TECH ZHEJIANG UNIV ZHEJIANG

Beta hairpin antimicrobial peptide containing d-type proline and glycine turn angle and preparation method thereof

The invention provides a β-hairpin antimicrobial peptide containing D-type proline and glycine corners and a preparation method thereof. The sequence of the antimicrobial peptide WKFpG of the present invention is shown in SEQ ID No.1. The present invention uses the rigid D-Pro-Gly corner as the corner unit, symmetrically places tryptophan and lysine at the non-hydrogen bond site of the β-hairpin side chain, and uses its interaction to assist the D-Pro-Gly corner to form a hairpin Structure, designed antimicrobial peptide template XWYKYZZXWYKY‑NH 2 . The application of the antibacterial peptide in the preparation of drugs for treating infectious diseases caused by Gram-positive bacteria and / or Gram-negative bacteria. The length of the amino acid sequence of this antibacterial peptide is only 12, which reveals the influence of rigid pG turn on the biological activity of β-hairpin antibacterial peptide, and has high inhibitory effect on various Gram-negative bacteria and positive bacteria, and has low hemolytic activity , the therapeutic index reaches 110.30, which is 1.5 times higher than that of the β-hairpin antimicrobial peptide with the same side chain containing NG turn, and has the potential to become a green and efficient antibiotic substitute.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Beta-hairpin antimicrobial peptide with cross-chain interaction between tryptophan and histidine and preparation method of beta-hairpin antimicrobial peptide

The present invention provides a beta-hairpin antimicrobial peptide with cross-chain interaction between tryptophan and histidine and a preparation method of the beta-hairpin antimicrobial peptide. The antimicrobial peptide WHFPG has a sequence shown in SEQ ID No.1. The preparation method utilizes an arrangement principle of a beta-hairpin structure, the interaction between the tryptophan and histidine forms mutual attraction of two beta-side chains, a PG corner is used as a central corner unit to obtain a stable beta-hairpin amphiphilic antimicrobial peptide template XWYHYPGXWYHY-NH2, whereinX=R and Y=F. The antimicrobial peptide is applied in preparation of medicines for treating infectious diseases caused by gram-positive bacteria or / and gram-negative bacteria. The antimicrobial peptide can work under both a neutral pH condition and an acidic pH condition, can inhibit the gram-negative bacteria more powerfully under the acidic pH condition, has a therapeutic index of 211.68, and has a wider clinical application potential.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Antimicrobial peptide yhx-3 and its composition and application

The invention belongs to the field of biotechnology, and in particular relates to an antimicrobial peptide YHX‑3 and its composition and application. The amino acid sequence of the antimicrobial peptide YHX‑3 is shown in SEQ ID No.1. The antimicrobial peptide YHX-3 provided by the present invention has broad-spectrum antibacterial activity, and is effective against Gram-positive bacteria and All Gram-negative bacteria have significant antibacterial activity; and their hemolytic activity is low, the sequence length is short, the molecular weight is small, and the chemical synthesis is less difficult. It can kill pathogenic bacteria in organisms more specifically and save scale. Cost of production.
Owner:OCEAN UNIV OF CHINA

I and i+4 site-directed mutation of porcine tp peptide highly active derivative antibacterial peptide and its preparation method and application

The present invention provides an antimicrobial peptide of i and i+4 site-directed mutation highly active derivatives of porcine TP peptide and its preparation method and application. The sequence of the antibacterial peptide TP(i+4)5 is shown in SEQ ID No.1. Select the porcine TP peptide, replace the paired amino acids on the hydrophilic surface of the porcine TP peptide with lysine at the hydrogen bond formation position (i, i+4), and obtain a peptide with the best effect TP(i+4)1 , 2. On the basis of it, tryptophan is used to replace the amino acid at position (i, i+4) to increase the hydrophobic surface of the antimicrobial peptide, and obtain an antimicrobial peptide TP(i+4) with high activity, low toxicity and high stability )5, and has a lower hemolytic activity; and discloses the application of the antibacterial peptide TP(i+4)5 in the preparation of antibacterial drugs for the treatment of Gram-negative bacteria and / or Gram-positive bacterial infectious diseases. The antimicrobial peptide of the present invention has the development potential of becoming a substitute for high-efficiency antibiotics.
Owner:NORTHEAST AGRICULTURAL UNIVERSITY

Stapled peptide conjugate for degrading MDM2/MDMX protein by protein-targeted chimera and application thereof

The invention relates to the field of polypeptide drugs, in particular to a stapled peptide conjugate for degrading MDM2 / MDMX protein by protein-targeted chimeras (PROTACTs) and a preparation method and application thereof. The stapled peptide conjugate is composed of three parts: a first peptide fragment suitable for binding with the MDM2 / MDMX protein, a second peptide fragment suitable for binding with E3 ubiquitin ligase VHL, and a connecting arm enabling the first peptide fragment and the second peptide fragment to be connected. The E3 ubiquitin ligase VHL can be used for carrying out ubiquitination modification on the MDM2 / MDMX protein, so that protease degrades the ubiquitination MDM2 / MDMX protein, a P53 factor is activated to play roles in killing cancer cells and inhibiting tumor formation ability, and the E3 ubiquitin ligase VHL has a potential application value.
Owner:THE NAVAL MEDICAL UNIV OF PLA

Method for preparing degradable organic-inorganic nanometer hybrid material containing POSS (Polyhedral Oligomeric Silsesquioxanes)

The invention discloses a method for preparing a degradable organic-inorganic nanometer hybrid material containing POSS (Polyhedral Oligomeric Silsesquioxanes), comprising the following steps of: (1) firstly, preparing a difunctional POSS derivative (II) by carrying out the addition reaction of amino POSS (I) and 2-hydroxyethyl acrylate through Michael; and (2) secondly, forming an etherified product by carrying out the esterification reaction of aromatic dibasic acid and aliphatic dihydric alcohol and preparing the degradable organic-inorganic nanometer hybrid material containing the difunctional POSS through the melt polycondensation reaction of the difunctional POSS derivative (II) and aliphatic chydroxy oligomer with the etherified product. The preparation method has the advantages ofuniform dispersion and difficult agglomeration of POSS in the hybrid material during preparation, effective improvement on the performances of degradable copolyester composite material, simple operation and high yield.
Owner:NINGBO INST OF TECH ZHEJIANG UNIV ZHEJIANG
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