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70 results about "New Zealand Rabbit" patented technology

One of the larger rabbit breeds, the New Zealand was derived by Don Johnson in 1916 by crossing unknown breeds. This rabbit weighs between 9-12 lbs. fully grown and may come in a variety of coat colors.

Kit for rapid detection of staphylococcus aureus in sample and detection method thereof

The invention discloses a kit for rapid detection of staphylococcus aureus in a sample and a detection method thereof, belonging to the technical field of immunological detection. In the invention, a staphylococcus aureus immunogen inactivated with formaldehyde is used for immunizing a healthy New Zealand rabbit to obtain a polyclonal antibody to serve as a coated antibody, and used for immunizing a BALB / C mouse and performing cell fusion to obtain a monoclonal antibody to serve as a secondary antibody, thus, the kit for performing a double antibody sandwich enzyme-linked immunosorbent assay on the staphylococcus aureus in food (milk) is established, and a rapid and efficient detection means is provided for residual detection of the staphylococcus aureus in the food, and the advantages of lower cost and better stability and repeatability are achieved. A detection limit of the kit is 105cfu / mL and is suitable for detecting mass samples.
Owner:JIANGNAN UNIV

Water body Chlamydomonas reinhaidtii toxin detection method

The invention relates to a measuring method of micro-capsule alga toxin in water. The method includes the steps as follows: firstly, compounding and appraising of the micro-capsule alga toxin; secondly, preparing and purifying of polyclonal antibody antibody: immunizing the New-Zealand rabbit by making the micro-capsule alga toxin holoantigen MC-LR-KLH as the immunity resource, and preparing the polyclonal antibody and purifying by ammonium sulphate according to the normal method; thirdly, preparing immune bead: coupling the micro-capsule alga toxin holoantigen MC-LR-BSA and the nanometer bead, and preparing the immune bead containing MC-LR-BSA; fourthly, embedding the antibody to the pyroxylin film; fifthly, producing testing board, combing the coupling mat of the magnetic scale MC-LR-BSA, the pyroxylin film embedding the polyclonal antibody, the sample mat, the sopping mat, the covering film, the testing board out card into a testing board; sixthly, sample testing, respectively adding standard goods and testing samples with different concentrations into the sampling holds on the testing board, the samples flow on the test paper through the chromatography effect, after 3 to 5 minutes of the reaction under the room temperature, the testing board is put into a magnetic single testing apparatus to be tested, and the testing apparatus can further output the biology reaction signals being transferred to the magnetic field signals by the way of the electric signals; after the standard curve being drawn, the specific value of the micro-capsule alga toxin content in the sample to be tested is counted based on the standard curve.
Owner:嘉兴博泰生物科技发展有限公司

Method for establishing animal model infected with Acinetobacter baumannii pneumonia

The invention discloses a method for establishing an animal model infected with Acinetobacter baumannii pneumonia. The method comprises the following steps: (1) preparing an immunosuppressive New Zealand rabbit; (2) preparing an Acinetobacter baumannii solution; (3) infecting the animal and establishing the model. The simple, rapid and efficient animal model infected with Acinetobacter baumannii pneumonia is established to help people research production and development processes of drug resistance of Acinetobacter baumannii and drug resistance related mechanisms of the Acinetobacter baumannii, assistance is provided for delaying of drug resistance of bacteria and better treatment of infection with the Acinetobacter baumannii, expense for related treatment of patients can be reduced, and human health can be promoted.
Owner:湖南斯莱克景达实验动物有限公司

TgVP1 extracellular region antigen polypeptide, anti-TgVP1 polyclonal antibody and application of polyclonal antibody

The invention discloses a toxoplasma gondii TgVP1 extracellular region antigen polypeptide, an anti-toxoplasma gondii TgVP1 polyclonal antibody and the application of the polyclonal antibody. The amino acid sequence of the toxoplasma gondii TgVP1 extracellular region antigen polypeptide is as shown in SEQ ID NO: 1 or a sequence as shown in SEQ ID NO: 1 of which the N end is connected with a cysteine. A New Zealand rabbit is immunized by the toxoplasma gondii TgVP1 extracellular region antigen polypeptide as an immunogen so that the anti-toxoplasma gondii TgVP1 polyclonal antibody can be obtained; an identification result indicates that the polyclonal antibody is capable of specifically identifying the toxoplasma gondii TgVP1 protein and can be applied to the detection of the toxoplasma gondii TgVP1 protein in tests such as ELISA, Western blot and immunofluorescence. A powerful tool is provided for the fundamental research of the protein functions and the research of the protein as a potential anti-toxoplasma gondii drug target; in short, the polyclonal antibody is wide in application prospect.
Owner:SOUTHERN MEDICAL UNIVERSITY

Toxoplasma gondii TgVP1 extracellular region antigen polypeptide, anti-toxoplasma gondii TgVP1 polyclonal antibody and application of polyclonal antibody

The invention discloses a toxoplasma gondii TgVP1 extracellular region antigen polypeptide, an anti-toxoplasma gondii TgVP1 polyclonal antibody and the application of the polyclonal antibody. The amino acid sequence of the toxoplasma gondii TgVP1 extracellular region antigen polypeptide is as shown in SEQ ID NO: 1. A New Zealand rabbit is immunized by the toxoplasma gondii TgVP1 extracellular region antigen polypeptide as an immunogen so that the anti-toxoplasma gondii TgVP1 polyclonal antibody can be obtained; an identification result indicates that the polyclonal antibody is capable of specifically identifying the toxoplasma gondii TgVP1 protein and can be applied to the detection of the toxoplasma gondii TgVP1 protein in tests such as ELISA, Western blot and immunofluorescence; a powerful tool is provided for the fundamental research of the protein functions and the research of the protein as a potential anti-toxoplasma gondii drug target; in short, the polyclonal antibody is wide in application prospect.
Owner:SOUTHERN MEDICAL UNIVERSITY

Method of in-vitro expression of gekko japonicus Hoxc10 (homebox gene c10) protein and preparation of polyclonal antibody

The invention discloses a method of the in-vitro expression of a gekko japonicus Hoxc10 (homebox gene c10) protein and the preparation of a polyclonal antibody, comprising the following steps of: obtaining an EST (Expressed Sequence Tag) sequence of gekko japonicus Hoxc10; obtaining an overall length sequence of the gekko japonicus Hoxc10 through an RACE (rapid amplification of cDNA ends) method; predicting an antigenic epitope of the gekko japonicus Hoxc10 protein on line by adopting DNASTAR software and SWISS-PLOT; constructing a prokaryotic expression vector of the gekko japonicus Hoxc10 by selecting superior epitope peptides; inducing the expression of fusion proteins in vitro; purifying the fusion proteins; preparing the polyclonal antibody, and the like. In the invention, an in-vitro gekko japonicus Hoxc10 expression system constructed on the basis of pGEX-4T1 can efficiently express a target protein in BL21 and further purify the target protein; and a large quantity of GST-Hoxc10 fusion proteins can be conveniently obtained; in addition, a rabbit gekko japonicus Hoxc10 antiserum prepared by immunizing a New Zealand rabbit through the GST-Hoxc10 fusion proteins has high titer and good specificity.
Owner:NANTONG UNIVERSITY

Polyclonal antibody for efficiently recognizing proteinserine heptanose glycosylation, and reparation method and application thereof

The invention relates to a polyclonal antibody for efficiently recognizing proteinserine heptanose glycosylation, and a reparation method and application thereof. The antibody is used for detecting different structures of natural protein modified by proteinserine heptanose glycosylation and screening and discovering novel antibiotics. The preparation process of the antibody comprises the steps offirstly building a C7 sugar framework by Wittig reaction; then, obtaining six-bit heptose of two absolute structures through Sharpless asymmetrical oxidization reaction; under the help of glucosinolates and trichloroacetimidate mediated glycosylation reaction, obtaining proteinserine heptanose with the same glycosylation modification structure in the organism; then, obtaining the corresponding glycopeptide with the sequence being Ac-GS(Hep)GL-OH by using a polypeptide solid phase synthesis method; coupling the obtained semi-antigen onto the carrier protein BSA to obtain antigen; immunizing animals by the antigen; collecting immunized New Zealand rabbit blood to prepare antiserum; obtaining IgG through affinity purification. The prepared antibody has high specificity and high valence.
Owner:SECOND MILITARY MEDICAL UNIV OF THE PEOPLES LIBERATION ARMY

Antigenic polypeptide of poplar functional centromere histone CENH3 and application thereof

The invention discloses an antigenic polypeptide of poplar functional centromere histone CENH3 and application thereof, belonging to the fields of bioinformatics and molecular cytogenetics. The invention mainly comprises the following steps: screening a specific amino acid sequence of populus tomentosa CENH3 protein and artificially synthesizing a polypeptide; immunizing New Zealand rabbits with the polypeptide to prepare antiserum; and carrying out affinity purification to obtain a CENH3 protein antibody. Immunofluorescence detection and ChIP-FISH are carried out on the antibody to verify thespecificity, thereby proving that the antibody can accurately identify the functional centromere. The antibody can be universally used in poplar species, can accurately mark the position of the poplar functional centromere, and lays a foundation for developing the research on the structure, function and evolution of the poplar functional centromere. The invention has wide application prospects inthe research fields of poplar molecular cytogenetics, genomics, epigenomics and the like.
Owner:NANJING FORESTRY UNIV
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