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42 results about "CAR bacillus" patented technology

CAR bacillus is a Gram-negative, gliding bacterium that colonizes the ciliated epithelium of the respiratory tract consisting of the lungs, the middle ears, the trachea, larynx, and the nasal passages.

Automatic mycobacterium tuberculosis screening system for mycobacterium tuberculosis sputum smear

The invention discloses an automatic mycobacterium tuberculosis screening system for mycobacterium tuberculosis sputum smear, comprising a mycobacterium tuberculosis sample scanner, a control recognition system and a remote diagnosis system, wherein the mycobacterium tuberculosis sample scanner comprises an optical system for amplifying a mycobacterium tuberculosis sample, a high-precision slide glass platform for holding the mycobacterium tuberculosis sample, an illumination system and a control PC machine; the control recognition system comprises a mycobacterium tuberculosis sample scanning system, an intelligent mycobacterium tuberculosis recognition system and a mycobacterium tuberculosis image database management system; the control PC machine is in communication connection with the mycobacterium tuberculosis sample scanning system; the mycobacterium tuberculosis image database management system is connected with the intelligent mycobacterium tuberculosis sample recognition system by a mycobacterium tuberculosis sample image display and analyzing application module; the control recognition system is connected with the remote diagnosis system. According to the invention, the mycobacterium tuberculosis sputum smear is successfully digitalized by a fluorescent scanner, automatic scanning is realized, remote share of one mycobacterium tuberculosis sputum smear can be realized, and the mycobacterium tuberculosis sputum smear can be stored for a long time.
Owner:KONFOONG BIOTECH INT

Application of bacillus licheniformis rex gene to increase of yield of poly gamma-glutamic acid

ActiveCN110305917AIncrease productionImprove the ability to synthesize poly-γ-glutamic acidBacteriaMicroorganism based processesBacillus licheniformisGlycerol
The invention belongs to the technical field of genetic engineering and microorganisms, and particularly relates to an application of a bacillus licheniformis rex gene to increase of yield of poly gamma-glutamic acid. A molecular biology technique is adopted, a transcription inhibition factor gene rex is knocked out in bacillus licheniformis, a bacillus licheniformis engineering strain WX-02 Deltarex having rex deletion is obtained, and the glycerine metabolism rate of the bacillus licheniformis is notably increased. The glycerine consumption rate of the WX-02 Delta rex in different culture mediums is at least increased by 10.55% than that in an original bacterium namely bacillus licheniformis WX-02, and the highest glycerine consumption rate can reach 27.94%. Through the adoption of thestrain in the poly gamma-glutamic acid fermentation culture mediums, the yield of the poly gamma-glutamic acid can be notably increased, the yield is at least increased by 35.29%, and the yield can beat most increased by 50%, which illustrates that a genetic engineering reformation method has important effects in increasing the microorganism glycerine metabolism rate, and the efficiency of synthesizing biological based chemicals through glycerine can be improved.
Owner:HUBEI UNIV

Construction and application of tubercle bacillus Pup gene deletion mutation strain

The invention discloses a construction method and application of a tubercle bacillus Pup gene deletion mutation strain. Based on a fusion PCR technique and a T carrier cloning technique, a replacementtype deletion mutation carrier T-Pup-N-K-Pup-C of a gene is constructed and identified for the first time, through an electrotransformation technique, the recombinant Pup gene deletion mutation carrier enters mycobacterium tuberculosis competent cells, and through chromosome homologous recombination, multiple screening and identification, the tubercle bacillus Pup gene deletion mutation strain containing a kanamycin resistant gene is obtained for the first time. According to the tubercle bacillus Pup gene deletion mutation strain constructed by the construction method disclosed by the invention, a Pup gene in an MTB Pup-proteasome system is knocked out, so that the drug tolerance of a clinical drug-tolerance tubercle bacillus separation strain can be reduced, the clinical drug-tolerance tubercle bacillus separation strain can restore sensibility to tubercle resisting medicines, the ubercle bacillus Pup gene deletion mutation strain can help for exploring the pathogenic mechanism of MTB and controlling propagation of tuberculosis, and a new direction is provided for seeking a tubercle resisting drug target.
Owner:SHIHEZI UNIVERSITY

A double-antibody sandwich enzyme-linked immunosorbent assay for the detection of Pseudomonas syringae Pseudomonas syringae

The invention relates to a double-antibody enzyme-linked immunosorbent assay for detecting clove pseudomonas spot pathogenic and variant bacteria, which belongs to the field of the immunoassay. Inactivated clove pseudomonas spot pathogenic and variant inactivated bacteria are used for immunizing an 8-month-old BALB / c mouse, and six hybridoma cell strains for producing specific monoclonal antibodies can be obtained by virtue of immunization, cell fusion and screening. The six antibodies are respectively marked by HRP, and every two of the six antibodies are paired by adopting the clove pseudomonas spot pathogenic and variant bacteria as a target. The antibody 1D3 (CGMCCNo.9312 monoclonal cell strain Q) and the antibody 6C6 (CGMCCNo.9313 monoclonal cell strain R) are respectively used as a coating antibody and an ELISA antibody to establish the double-antibody enzyme-linked ELISA method of the clove pseudomonas spot pathogenic and variant bacteria, and LOD is 1.5*10<5>cfu / mL. By adopting the ELISA method to detect the double-antibody enzyme-linked immunosorbent assay for detecting clove pseudomonas spot pathogenic and variant bacteria, the specificity is good, the sensitivity is high, the cost is low, and the high-flux determination of the double-antibody enzyme-linked immunosorbent assay for detecting clove pseudomonas spot pathogenic and variant bacteria can be realized.
Owner:JIANGNAN UNIV
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