220 results about "Clenbuterol" patented technology

The present invention provides a clenbuterol monoclonal antibody and applications thereof. The present invention discloses a clenbuterol monoclonal antibody preparation method, wherein clenbuterol hapten is synthesized, the synthesized clenbuterol hapten and carrier protein are coupled to obtain clenbuterol antigen, and the clenbuterol antigen is adopted to immunize animals to obtain a high specificity monoclonal antibody. The present invention further provides a method for application of the clenbuterol monoclonal antibody in a clenbuterol enzyme-linked immunosorbent assay kit to detect clenbuterol. The present invention further provides a method for application of the clenbuterol monoclonal antibody in a clenbuterol colloidal gold test paper card to detect clenbuterol. The prepared clenbuterol monoclonal antibody has characteristics of high specificity and low cost, wherein the clenbuterol drug detection clenbuterol enzyme-linked immunosorbent assay kit prepared by using the clenbuterol monoclonal antibody and the clenbuterol drug detection clenbuterol colloidal gold test paper card prepared by using the clenbuterol monoclonal antibody have characteristics of convenient operation, high specificity, high sensitivity, high accuracy, high precision, fast detection and the like.

The invention discloses an immune chromatography test paper strip for the quantitative determination of clenbuterol based on up-conversion fluorescent nanoparticle label and a preparation method thereof. The test paper strip comprises a supporting layer, an adsorption layer, and a protection layer, wherein the adsorption layer comprises an adsorption fibrous layer, a fluorescent antibody fibrous layer, a cellulose film and an absorbent material layer at the handle end, the cellulose film is provided with detection blots printed by using a CL coupling carrier protein solution and control blots printed by using goat anti-mouse IgG antibodies, and the fluorescent antibody is an NaYF4:Yb:Er nanoparticle labelled CL monoclonal antibody or polyclonal antibody. According to the invention, the application of immune chromatography based on the up-conversion fluorescent nanoparticle label in the quantitative determination of CL residues is realized, so that the detection of the CL residues has no background interference; and the test paper strip has the advantages of strong specificity, high sensitivity, simple, and accurate detection, low cost, wide application scope, and easiness in popularization and application.

The invention relates to a novel synthesis method for a multilayer protection hyperstable water-soluble single fluorescent quantum dot and a fluorescent microsphere. The method comprises the following steps: transferring an oil-soluble fluorescent quantum dot to a water phase by using an amphoteric oligomer; then wrapping a water-soluble single fluorescent quantum dot and a fluorescent microsphere in silica; allowing the surfaces of the single fluorescent quantum dot and the fluorescent microsphere wrapped by silica to carry hydrophobic groups; and finally preparing the multilayer protection hyperstable water-soluble single fluorescent quantum dot and the fluorescent microsphere by using the amphoteric oligomer again. With the method, the fluorescent quantum dot can be protected from a destructive effect of an external environment (e.g., a strong acid, a strong alkali, a salt, etc.) to a greatest extent. The multilayer protection hyperstable water-soluble single fluorescent quantum dot and the fluorescent microsphere can be used in a microporous immunostrip biological detection system for detection of human chorionic gonadotropin (HCG), human immunodeficiency virus (HIV), hepatitis and clenbuterol--ractopamine(Rac) residual and the like in swine urine.

The invention relates to an enzyme couple immune detecting field, especially disclosing a clenobuterol enzyme immune agent box, relative detecting method, and a method for preparing the sample of animal organism, wherein said box comprises a box body, a 96 / 40 porous enzyme mark plate, a horse peroxide enzyme mark antibody, a clenobuterol standard solution, a substrate liquid, a substrate buffer liquid and a reaction ending liquid; the holes of said mark plate packs the packing antibody that combined with the clenobuterol antibody. The invention uses direct competitive enzyme couple immune adsorption analysis technique, to simplify the operation and reaction time, to reduce error. The inventive method has simple operation, low cost, and short time, while the extracted sample can be directly used in enzyme couple immune method and golden mark immune laminated analysis, to be sample of prior analysis.

The invention discloses a method for detecting clenbuterol residue in hair. The method sequentially comprises the following steps: (1) pre-processing a hair sample: hydrolyzing the sample with alkali at a high temperature, extracting the sample with an organic solvent and reversely extracting the sample with acid water; and (2) taking deuterated clenbuterol-D9 aqueous solution with the concentration of 5-500ng / ml as an internal standard, and detecting the clenbuterol residue in hair by liquid chromatogramy-tandem mass spectrometry. The method has the following advantages: 1. hair is taken as a detection material, which provides easy sampling, convenient storage and repeatable sampling, sampling is simple and rapid and has trace amount and high efficiency; 2. the pre-processing method of the hair sample is optimized, which shortens the pre-processing time, simplifies the processing steps and obviously reduces the cost; and 3. an isotopic compound is taken as the internal standard, and the liquid chromatogramy-tandem mass spectrometry is used as a detection means, the minimum detection limit reaches 0.01ng / g, and the minimum quantification limit is 0.5ng / g. The method has the accurate and reliable capacity to qualitatively and quantitatively detect the clenbuterol, and can be taken as a tool for large sample screening or small sample confirmation.

The invention discloses a hybridoma cell line secreting a monoclonal antibody repelling Clenbuterol hydrochloric acid, and an antibody repelling Clenbuterol hydrochloric acid through the hybridoma cell line. The invention also discloses a kit for detecting Clenbuterol hydrochloric acid residual. The kit comprises: a glowing black test board coated by CL-BSA in advance, a Clenbuterol hydrochloric acid standard liquid, an ELISA Clenbuterol hydrochloric acid antibody, a chemical luminescence liquid and a cleaning solution. The kid for detecting Clenbuterol hydrochloric acid residual has qualitative improvements on specificity, sensitivity and stability compared with the prior kit. The lowest detection value of Clenbuterol (CLB) hydrochloric acid residual is 0.02 ng / L, thereby completely meeting the requirements of detecting the level CLB residual.

The invention relates to a preparation method and application of a miniature high-efficiency clenbuterol immuno-affinity chromatography column. The technical scheme is characterized by comprising the following steps of: preparing a high-quality antibody, synthesizing efficient prepared bromoacetyl chloride clenbuterol purified by a liquid chromatogram and thiolation hemocyanin into immunogen immune animals, and obtaining antiserum; reacting the purified bromoacetyl chloride clenbuterol with thiolation agarose to obtain clenbuterol-agarose padding, loading the padding into an antigen affinity chromatography column; and purifying a clenbuterol specific antibody in the antiserum by using the antigen affinity chromatography column. The preparation method of the clenbuterol immuno affinity chromatography column comprises the following steps of: coupling high-quality antibodies at high density to the agarose oxidized by periodic acid to prepare an antibody affinity padding, and placing 25 mul of padding in a small specially-made column to prepare the miniature immuno-affinity chromatography column. The immuno-affinity chromatography column provided by the invention can be used for specifically gathering clenbuterol in a sample to be tested at high efficiency and can increase the accuracy, reliability and sensitiveness of detection when being combined with an analytic instrument and colloidal gold test paper for use.

The invention relates to a production method of a clenbuterol molecularly imprinted-upconversion luminescent material fluorescence probe. The probe is a novel fluorescence probe produced through combining an upconversion luminescent material YF3:Yb<3+>, Er<3+> as a carrier with a covalent bond technology prepared clenbuterol molecularly imprinted polymer. The probe combines the high specific identification performance of the molecularly imprinted polymer with the high sensitivity of the upconversion luminescent material. The production method comprises the following steps: preparing the upconversion luminescent material, preparing the clenbuterol molecularly imprinted-upconversion luminescent material fluorescence probe, and eluting clenbuterol molecules. The fluorescence probe produced in the invention emits visible light under the excitation of infrared light, and has the advantages of high sensitivity, strong specificity and small interference. The production method has the advantages of simplicity, good reappearance, and good application prospect in selective identification and detection of clenbuterol in a practical sample.

The invention discloses a method and a special chemical luminous immunoassay kit for detecting clenbuterol. The special chemical luminous immunoassay kit for detecting clenbuterol comprises a clenbuterol specific antibody, a coating antigen and standard solution; and the coating antigen is a coupling compound of a clenbuterol hapten and a carrier protein. The detection method has the characteristics of simple sample preprocessing process, simple and convenient operation, low cost, high specificity, high sensitivity, high accuracy and the like, can perform monitoring on site and is suitable for screening a large number of samples.