289 results about "Aflatoxin B" patented technology

The present invention belongs to the field of biological detection. Multi-line immunochromatographic test strip for semi-quantitative detection of aflatoxin B1 comprises a paperboard, wherein a water-absorbing pad, a detection pad, a gold-labeled pad and a sample pad are adhered sequentially on one surface of the paperboard from top to bottom, wherein each adjacent pads is overlapped and connected, the detection pad uses a nitrocellulose film as a backing pad, the nitrocellulose film is provided with a transverse control line, a test line I, a test line II and a test line III, wherein the control line is coated with a rabbit anti-mouse polyclonal antibody, and the test line I, test line II and test line III are coated with aflatoxin B1-bovine serum albumin conjugate (AFB1-BSA), respectively: and the gold-labeled pad is transversely coated with a nanogold-labeled anti-aflatoxin B1 monoclonal antibody. Said test strip is used for semi-quantitative detection of aflatoxin B1, and is characterized by quick detection, simple procedure and high sensitivity.

The invention relates to an aflatoxin B1 flow lag immunization time distinguishing fluorescence rapid-detection kit and an application thereof. The kit comprises a fluorescent test strip and a sample reaction bottle containing an europium-labeled anti-aflatoxin B1 monoclonal antibody lyophilized product, wherein the fluorescent test strip comprises a cardboard, a water absorption pad, a detection pad and a sample pad are sequentially pasted on one surface of the cardboard from top to bottom, adjacent pads are connected at the connection in an overlapping manner, the detection pad treats a cellulose nitrate membrane as a base pad, a transverse quality control line and a detection line are arranged on the cellulose nitrate membrane from top to bottom, the quality control line is coated with a rabbit anti-mouse polyclonal antibody, and the detection line is coated with an aflatoxin B1 bovine serum albumin conjugate; and the anti-aflatoxin B1 monoclonal antibody is secreted by a hybridoma cell strain having a preservation number of CCTCC NO.C201015. The kit can be used for the quantitative determination of the content of the aflatoxin B1, and has the advantages of simple operation, rapidness and high accuracy.

The invention discloses a method for degrading aflatoxin, which makes use of gamma rays to irradiate a sample containing the aflatoxin, wherein the gamma rays are generated by a radioactive substance Co, and the irradiation dose is between 0 and 10 kGy not including 0, preferably between 2 and 10 kGy, more preferably between 4 and 10 kGy, particularly preferably between 6 and 10 kGy, and the most preferably 10 kGy. The sample containing the aflatoxin is a farm product containing the aflatoxin or a product obtained by processing the farm product, such as food, feedstuff, and the like. The method is particularly applicable to degrading the aflatoxin B1, not only can kill pathogenic microorganisms but also can degrade biotoxin therein, and does not generate any industrial pollution.

The invention discloses a complex microbial agent for producing soybean paste in Pixian County, which mainly comprises coculture of saccharomyces cerevisiae, candida utilis, lactobacillus plantarum and salt tolerant tetrads, and skim milk powder, glycerin, maltodextrin, trehalose and L-sodium glutamate, or mainly comprises coculture of saccharomyces cerevisiae, candida utilis, lactobacillus plantarum and salt tolerant tetrads, and porous starch, maltodextrin and polyvinyl pyrrolidone. A method for preparing the complex microbial agent for producing soybean paste in Pixian County comprises the following technological steps of: (1) activating and propagating strains; (2) inoculating; (3) co-culturing; and (4) adding a protective agent and drying. By using the complex microbial agent in the preparation of cooked soybean paste, the complex microbial agent maintains the characteristics of traditional soybean paste in Pixian County. Meanwhile, compared with the traditional technology, the complex microbial agent has the advantages of shortening the production period by 1 / 3, improving the amino nitrogen content by 3 to 8 times, improving the volatile aroma content by 2 to 4 times, and ensuring the aflatoxin B1 of 0 to 0.5ppm only.

The present invention is fast detection method of aflatoxin B1 in food and feed. The fast detection method includes the following steps: adding ground sample to be tested in 2-10 g in test tube, adding methanol-sodium chloride aqua of 50-80 % concentration in 10-25 ml, ultrasonic extraction in water bath at 40-60 deg.c, and suction filtering to obtain filtrate in 4-10 ml; adding re-distilled petroleum ether in 2-4 ml into the filtrate, shaking, letting stand to laminate, taking the lower layer of solution in 1-4 ml and adding pure water in 4-20 ml; adding to micro immunoaffinity column of aflatoxin B1, washing with methanol aqua of 10-40 % concentration in 5-10 ml, eluting with methanol in 0.5-2.0 ml, collecting the eluted liquid, adding test agent A in 0.2-1.0 ml; and detecting in fluorescent spectrophotometry or similar instrument. The present invention has the features of simple process, high detection precision and stability, fast detection speed and high safety.

The invention provides an aflatoxin B1 (AFB1) magnetic separation enzyme-linked immunity quantitative detection method, belonging to the field of food safety immunoassay technique. The method adopts the immuno-detection principle of competition law; and AFB1 is connected with biological enzyme to prepare enzyme-labeled antigen reagent, anti-fluorescein isothiocyanate (FITC) antibody is absorbed onthe surfaces of magnetic particles to prepare magnetic separation reagent, and the FITC is connected with the AFB1 antibody to prepare anti-reagent. In a sample, the AFB1 competes with the enzyme-labeled AFB1 and is combined with a small amount of FITC-labeled anti-AFB1 antibody, so that antigen-antibody complex can be formed. After the magnetic separation reagent is added, the complex is caughtonto the surfaces of the magnetic particles by the anti-FITC antibody connected on the surfaces of the magnetic particles. After being washed, the product is finally added with substrate and detected.The method has the advantages that (1) the magnetic particles are used for replacing the traditional enzyme-labeled plate to be taken as a solid-phase carrier, so that immunoreaction is carried out under the approximate liquid phase condition; and the reaction is more complete and rapid, and has the characteristics of high specificity and good repeatability compared with the traditional enzyme-linked immuno sorbent assay (ELISA); furthermore, (2) by adopting one-step competition law principle, the time used for detection is short.

The invention relates to the field of bioengineering, in particular to a preparation method and an application of a microbial agent composition for enhancing secondary fermentation of a bean paste. The microbial agent composition consists of a saccharomycetes agent, an aspergillus oryzae agent and a pleospora agent; and the three microbial agents are prepared, and then the prepared microbial agents are mixed with the secondary-fermented bean paste, so as to promote the secondary fermentation of the bean paste. The whole process of the preparation method of the microbial agent composition provided by the invention is applicable to continuous industrial production; by-products (chili and radix platycodonis), from the production of Pixian bean paste, are comprehensively utilized; a production cycle can be shortened by 6 months, the content of amino nitrogen can be improved by 20% and the content of volatile aroma-producing components can be improved by more than 3 times (the contents of total ester, total acid and total aldehyde); by inoculating aflatoxin B1 with the saccharomycetes agent at a production peak (after being fermented for 30-60 days), an ester producing and aroma generating process can be enhanced, the metabolism of aspergillus flavus and partial aspergillus parasiticus can be competitively inhibited and the content of the aflatoxin B1 can be reduced, and the content of the aflatoxin B1 is lower than 0.5ppm, so that food safety is enhanced.

The present invention relates to a hybridoma cell line 3G1 and an anti-alfatoxin B1 monoclonal antibody produced by the hybridoma cell line 3G1. The hybridoma cell line 3G1 (CCTCCNO.C201014) can be used for preparation of a high titer anti-aflatoxin B1 monoclonal antibody, wherein an enzyme-linked immunosorbent assay (ELISA) method is adopted to determine a titer, and the titer is 6.40*10<6>. The anti-aflatoxin B1 monoclonal antibody of the present invention has characteristics of high sensitivity and good specificity, wherein 50% inhibiting concentration on aflatoxin B1 by the monoclonal antibody is 1.6 ng / mL, cross reaction rate with aflatoxin B2 is 6.4%, and cross reaction rates with aflatoxin G1 and G2 are less than 1%. In addition, the anti-aflatoxin B1 monoclonal antibody of the present invention can be used for determination of aflatoxin B1.

The invention belongs to the field of biological detection and provides a high-sensitivity immunochromatographic test strip for detecting total aflatoxin content quickly, which is characterized by comprising a test strip, wherein a water-absorbing pad, a detection pad, a gold label pad and a sample pad are adhered on one side of the test strip from top down; the pads are overlapped at the connected parts; the detection pad uses a nitrocellulose film as a substrate pad; transverse quality control lines and detection lines are arranged on the nitrocellulose film from top down; the detection lines are coated with aflatoxin B1-bovine serum albumin (AFB1-BSA) coupling and the quality control lines are coated with rabbit anti-mouse polyclonal antibody; and a nano gold-labeled anti-aflatoxin common monoclonal antibody, which is generated by hybrid tumor cell strain 1C11 having a collection number of CCTCC No.C201013, is sprayed on the gold label pad transversely. The test strip is used for detecting total aflatoxin content and has the characteristics of quick detection, simple operation and high flexibility.

The invention discloses a test strip for detecting aflatoxin B1 or M1 by utilizing an aptamer. The test strip for detecting the aflatoxin B1 or M1 by utilizing the aptamer, provided by the invention, comprises a sample absorption pad, a marker pad, a reaction film and a water absorption pad, wherein the marker pad is coated with a detection probe; the detection probe is an aflatoxin B1 aptamer marked by fluorescein; the nucleotide sequence of the aflatoxin B1 aptamer is sequence 1; the reaction film comprises a detection region and a quality control region; the detection region is coated with a conjugate formed by an aflatoxin B1 hapten and a carrier protein; and the quality control region is coated with a quality control probe, and the quality control probe is a conjugate formed by avidin conjugation probe marked aflatoxin B1 complementary single strand DNA (Deoxyribose Nucleic Acid)) molecules. The test strip for detecting the aflatoxin B1 or M1, provided by the invention, has the advantages of high sensitivity, accuracy in quantifying, strong specificity, simplicity and convenience, and short detection time.

The invention discloses a group of oligonucleotides aptamers capable of specifically recognizing aflatoxin B1. A single-chain deoxyribonucleic acid (DNA) oligonucleotides aptamer capable of specifically recognizing the aflatoxin B1 is acquired by a systematic evolution of ligands by exponential enrichment (SELEX) technology; the aptamer can be transformed into a report aptamer by a fluorescein mark and the like; the report aptamer is used for detecting the aflatoxin B1; and the aptamer sequence can accurately and rapidly check the aflatoxin B1 in the food; and therefore, the oligonucleotides aptamer has the wide application prospect.

The invention provides an enzyme-linked immunosorbent assay kit for detecting an aflatoxin B1-containing medicine and an application for the same. The enzyme-linked immunosorbent assay (ELISA) kit comprises an ELISA plate coated with a coating antigen, an enzyme label, aflatoxin B1 specific antibody working solution (contained in the case that the coating antigen on the ELISA plate and the enzyme label are enzyme-labelled antibodies or enzyme-labelled antigens), aflatoxin B1 standard substance solution, substrate developing solution, stopping solution, concentrated washing solution and concentrated compound solution. The method for detecting aflatoxin B1 by virtue of the kit provided by the invention comprises the following steps of: performing sample pre-treatment at first, and then detecting by virtue of the kit, and finally analysing the detected result. The enzyme-linked immunosorbent assay kit provided by the invention can be used for detecting the residual amount of aflatoxin B1 in samples such as oil, peanuts and grains, as well as is simple and convenient to operate, low in expense, high in sensitivity, capable of being monitored in the field, and suitable for screening lots of samples.

The invention discloses a bacillus amyloliquefacien for degrading aflatoxin B1 in peanut meal, and belongs to the technical field of applied microbiology. According to the invention, a bacillus amyloliquefacien capable of significantly inhibiting the growth of Aspergillus flavus and efficiently degrading aflatoxin B1 can be obtained by screening and the content of aflatoxin B1 in detoxified peanut meal is lower than the national limited standard and achieves the safe feeding level after the bacillus amyloliquefacien is applied to moldy peanut meal. Furthermore, the detoxification mechanism of the strain is the degradation effect of extracellular metabolites, and generation of the active substance is of a non-induced type, which is an inherent attribute of the strain. The features of the strain provide the possibility for biocontrol of Aspergillus flavus and aflatoxin B1 in industries such as feed and foods and the strain has very high application values.

The invention provides Lysobacter capable of efficiently degrading aflatoxin B1 and ochratoxin A and application of the Lysobacter and particularly provides double-function Lysobacter sp. CW239 and application thereof to the degradation of low-pollution concentration aflatoxin B1 and ochratoxin A. Compared with existing aflatoxin degrading bacteria, the Lysobacter sp. CW239 has the advantages that the Lysobacter sp. CW239 can achieve excellent degrading effect under a low-concentration toxin pollution condition; under a liquid fermentation condition, in fermentation broth, which contains the aflatoxin B1 and ochratoxin A, with the final concentration of 20 microgram / L, the 12-hour ochratoxin A degradation rate of the Lysobacter sp. CW239 is 53.1%, and the 48-hour degradation rate reaches 99.8%; the 12-hour aflatoxin B1 degradation rate of the Lysobacter sp. CW239 is 42.5%, and the 48-hour degradation rate reaches 83.4%; when the Lysobacter sp. CW239 is used for processing feed (with the final concentration of 20 microgram / kg) polluted by toxins, the 48-hour ochratoxin A degradation rate is 68.7%, and the 48-hour aflatoxin B1 degradation rate is 52.1%; the Lysobacter sp. CW239 has substantial application value and significance when being applied to food and feed bio-detoxification.

The invention belongs to the technical field of food safety detection, and provides a high-efficient liquid chromatogram method for simultaneously detecting aflatoxin B1, ochratoxin A, zearalenone and citrinin in grains. Universal type extracting solution is extracted, detection is realized by a high-efficeint liquid chromatogram and fluorescence detector method, and quantification is realized by an external standard method. Detection limits of the method respectively include 1.08 micro-grams / kg of aflatoxin B1, 3 micro-grams / kg of ochratoxin A, 35.85 micro-grams / kg of zearalenone and 6.52 micro-grams / kg of citrinin. The method is simple, convenient and fast, is low in environmental pollution and detection cost, and is applicable to simultaneously and quantitatively detect four types of mycotoxin in the grains.

The invention discloses a biosensor electrode for detecting aflatoxin B1 and a preparation method thereof. The biosensor electrode comprises a substrate layer and a reaction layer provided on the substrate layer. The reaction layer includes an electronic mediator, a sol-gel film and aflatoxin oxidase, wherein the electronic mediator is fixed on the substrate layer, and the sol-gel film embeds the aflatoxin oxidase on the substrate modified by the electronic mediator to form a film, thus obtaining aflatoxin oxidase modified electrode. The inventive biosensor electrode has the advantages of fast response, high signal sensitivity up to 1.5 ppm to 0.125 ppb, high specificity, convenient usage, quantitative detection, long service life and good stability.

The invention discloses a method for preparing an aflatoxin B1 aptamer affinity column and belongs to the field of affinity chromatography and mycotoxin analysis. The method comprises the following steps: adopting epoxy activated agarose microspheres FF as a solid phase carrier; after the solid phase carrier is coupled with an amino-modified aflatoxin B1 aptamer, closing extra active sites in the carrier, and feeding into micro columns. The prepared aptamer affinity column can be specially combined with aflatoxin B1, the adding standard recovery is 70-110, and the aptamer affinity column can be repeatedly used for at least five times.

The invention discloses a light induced chemiluminescent immunoassay reagent kit for aflatoxin B1and a detection method thereof, which belong to the technical field of light induced chemiluminescent immunoassay. A luminescent particle enveloped with AFB1-BSA is added into a microporosity plate, a AFB1 standard or sample, a rabbit anti-AFB1 antibody, a biotin goat anti-rabbit antibody are sequentially added for a photophobic reaction, then a photosensitive particle enveloped with streptavidin is photophobically added, and the mixture is incubated and then is detected. The AFB1-BSA enveloped on the luminescent particle competes with the AFB1 in the standard or sample for connecting to the AFB1 antibody to form a complex with the biotin goat anti-rabbit antibody and the photosensitive particle enveloped with the streptavidin, the energy is transferred to the luminescent particle to produce fluorescence by producing and transferring singlet ionic oxygen under optical excitation, a light induced chemiluminescent detector is used to detect, the intensity of optical signals is inversely proportional to the concentration of the AFB1, and the content of the AFB1 in the measured sample is determined by contrasting with the standard curve. The invention is used to detect the content of the AFB1 in foodstuff, feedstuff and products of the foodstuff and the feedstuff; and the reagent kit has the advantages of simple structure, simple and convenient operation, low cost, short detection time, and high sensitivity.

The invention discloses a preparation method of a composite microbial inoculant for degrading aflatoxin B1 and a composite microbial inoculant prepared by the method. The method comprises the following steps: respectively culturing pseudomonad, Flavobacterium, Rhodococcus, Stenotrophomonas and Bacillus to obtain a pseudomonad solution, a Flavobacterium solution, a Rhodococcus solution, a Stenotrophomonas solution and a Bacillus solution; mixing the pseudomonad solution, Flavobacterium solution, Rhodococcus solution, Stenotrophomonas solution and Bacillus solution to obtain a composite bacterium solution; and putting the composite bacterium solution into a composite bacterium culture medium, and carrying out mixed culture fermentation to obtain the composite microbial inoculant for degrading aflatoxin B1. The composite microbial inoculant can efficiently degrade aflatoxin B1, and has the advantages of low cost and no secondary pollution.

The invention relates to an immunochromatographic test strip for synchronously detecting mixed pollution of aflatoxin and zearalenone, a preparation method and application thereof. The test strip includes a paperboard. An absorbent pad, a detection pad, a gold labeled pad and a sample pad are sticked on one side of the paperboard from top to bottom. Adjacent pads are in overlapping connection at joints. The detection pad adopts a nitrocellulose membrane as a base pad, which is provided with a transverse control line and detection lines. The two detection lines in internal distribution are positioned below the quality control line, and are respectively coated with a zearalenone-bovine serum albumin conjugate and an aflatoxin B1-bovine serum albumin conjugate. The quality control line is coated with a rabbit antimouse polyclonal antibody. The gold labeled pad is horizontally sprayed with a nanogold labeled anti-aflatoxin universal monoclonal antibody and a nanogold labeled anti-zearalenone monoclonal antibody. The immunochromatographic test strip can be used for simultaneously detecting the content of fungaltoxins aflatoxin and zearalenone in a sample, and has the characteristics of simple operation, rapidity, and high sensitivity.

Disclosed are a lactic acid bacterium and application thereof. The lactic acid bacterium is capable of suppressing growth of mildew in fermented feed, reducing the content of aflatoxin B1 and improving the quality of the fermented feed. The technical scheme includes that the lactic acid bacterium is lactobacillus plantarum M-9 which is preserved in the China General Microbiological Culture Collection Center on 29th October, 2012, and the preservation number of the lactobacillus plantarum M-9 is CGMCC No.6740. The invention further discloses a method for preparing and using the lactic acid bacterium.

The invention belongs to the technical field of biosensors, and particularly relates to a preparation method for a ratio electrochemical biosensor for detecting aflatoxin B1. The composite material ofTHI (thionine) and rGO (reduced graphene oxide) is used as a first beacon molecule, ferrocene carried by AFB1 (Aflatoxin B1) aptamer is used as a second beacon molecule, and chitosan with positive electricity is used for connecting the first beacon molecule with the second beacon molecule through an electrostatic adsorption function and fixing the connected first beacon molecule and second beaconmolecule on the surface of a glassy carbon electrode. In the preparation method, the AFB1 aptamer is introduced, and the high specificity of the ratio electrochemical biosensor toxin AFB1 is improved. Two ends of the aptamer are designed to mark with an Fc signal to realize the amplification of a contrast ratio signal. The detection linear range of the constructed ratio electrochemical biosensoris 0.01ng.mL<-1>-100ng.mL<-1>, and the detection limit is 3.3pg. mL(-1). Through research, the preparation method for the sensor is simple, high in selectivity, sensitivity and reproducibility, is good in stability and provides a good sensing platform for detecting the AFB1 in a practical sample.

The invention relates to a method for removing aflatoxin in a plant raw material. The method comprises the following steps: adjusting pH of the plant raw material to be alkaline, inoculating a lactic acid bacteria culture solution to an alkaline plant raw material, carrying out anaerobic solid fermentation on the inoculated plant raw material to remove the aflatoxin in the plant raw material, finally detecting the content of aflatoxin by using a high-pressure liquid chromatography. According to the method, the conventional process of removing the aflatoxin in the plant raw material is changed; an anaerobic solid fermentation method is adopted; the aflatoxin in the plant raw material is greatly removed; in addition, the method is simple in process, good in degradation effect and suitable for degradation of the peanut meal aflatoxin; the removal rate of aflatoxin B1 reaches 100%; the method is high in application value and market potential.

The invention discloses a method for preparing a method capable of adsorbing aflatoxin and zearalenone. The method comprises the following steps: (1) dispersing montmorillonite in a 0.4-0.8wt% sodium modification agent solution, uniformly stirring, stirring at the temperature of 60-90 DEG C for 1-3 hours, and regulating the pH value to 9.5-10.5 by using a sodium hydroxide solution after a sodium modification reaction is ended; (2) adding a quaternary ammonium salt surfactant and mixing at the temperature of 60-90 DEG C for 2-5 hours; and (3) standing and settling the obtained precipitate, drying and crushing, thus obtaining the finished product, wherein the following materials are used in parts by weight: 30-100 parts of montmorillonite, 200-700 parts of 0.4-0.8wt% sodium carbonate and 5-25 parts of quaternary ammonium salt surfactant. The method is simple in process, and the finished product prepared by the method is high in stability, high in adsorption speed and excellent in adsorption property and can simultaneously adsorb aflatoxin B1 and zearalenone.

The invention discloses bacillus subtilis for degrading aflatoxin B1 and application of the bacillus subtilis, and belongs to the field of biotechnologies. Primary screening is carried out by the aid of courmarin which is used as a unique carbon source and a unique energy source, AFB1 (aflatoxin B1) degradation rates of strains are used as secondary screening indexes, and accordingly the bacillus subtilis S1 (CCTCC NO:M 2016390) capable of efficiently degrading the AFB1 can be obtained by means of screening. The bacillus subtilis and the application have the advantages that the AFB1 degradation rate of strain fermentation broth can reach 61.36%; the degradation rate can reach 80.26% after the bacillus subtilis is cultured according to an inoculation amount of 10%; the degradation rate can reach 85.65% after fermented supernatant is concentrated by 8 times; as shown in research, the aflatoxin B1 can be degraded by extracellular enzymes secreted by the bacillus subtilis S1, and accordingly the strain fermentation broth or active proteins separated from the strain fermentation broth can be used for degrading the aflatoxin B1 or preparing biological additives for degrading the aflatoxin B1.

The invention relates to a test paper card for synchronously detecting zearalenone and aflatoxin B1, and a preparation and a detection method, and belongs to the field of immunology detection. The test paper card comprises a card shell and a test paper strip, wherein the test paper strip comprises a bottom plate, a water absorption pad, a detection pad, a combination pad and a sample pad; the water adsorption pad, the detection pad, the combination pad and the sample pad are overlapped and pasted to the bottom plate in sequence; the detection pad is an NC membrane (nitrocellulose filter membrane) provided with a quality control line C, a detection line T1 and a detection line T2; the quality control line C coats a goat-anti-mouse second antibody, the detection line T1 coats ZEN-BSA, and the detection line T2 coats AFB1-BSA; the combination pad is a glass cellulose membrane which embeds an anti-zearalenone monoclonal antibody marked by time resolution fluorescent microspheres and anti-aflatoxin B1 monoclonal antibody; the sample pad is the glass cellulose membrane obtained in a way that drying is carried out after the dipping processing of sample pad conditioning fluid. The invention provides a new method for systematically, conveniently, normatively, quantitatively and synchronously detecting the zearalenone and the aflatoxin, stability is good, and sensitiveness is high.

The invention discloses a method for preparing mycotoxin adsorbent for an efficient carbon silicon feed by taking rice hulls as raw materials. The method comprises the following steps of: removing impurities from the rice hulls; pre-carbonizing the rice hulls; dissolving the pre-carbonized rice hulls in alkali liquor to remove silicon; activating and sintering the rice hulls and the like. According to the method, a porous carbon silicon composite material with different specific surface areas and total pore volumes is prepared from the rice hulls, which are abundant in source, low in cost and reproducible, serving as the raw materials, under the process conditions of the control of pre-carbonization, silicon removal by alkali dissolution, high-temperature active sintering and the like, so that the requirements of each industry on adsorbing materials are met. The mycotoxin adsorbent has obvious effects on the adsorption and reservation of aflatoxin B1, an adsorption rate is up to about 99 percent, and the adsorption stability is obvious, so the method has a bright prospect in the field of the processing of grain feeds.

The invention discloses an ultra-sensitive aflatoxin B1 enzyme-linked immunosorbent assay kit. The kit comprises an aflatoxin B1 standard solution, a solid phase carrier, an enzyme labeling object, a substrate developing solution, a sample dilute solution, a termination solution and a concentration washing solution, wherein the solid phase carrier is a micropore plate; and the enzyme labeling object is an aflatoxin B1 protein coupling object labeled by horseradish peroxide and is coated by an aflatoxin B1 monoclonal antibody, and the substrate developing solution is tetramethyl benzidine (TMB). The invention also discloses a preparation method of the ultra-sensitive aflatoxin B1 enzyme-linked immunosorbent assay kit and a method for detecting aspergillus flavus B1. By using the kit according to the invention to detect aflatoxin B1 the kit has the characteristics of simple operation, high sensitivity, good specificity, good linearity and the like.

The present invention relates to an aflatoxin B1 graphene oxide immunochromatographic test strip and application thereof. The aflatoxin B1 graphene oxide immunochromatographic test strip includes a chromatographic test strip and a carboxylated graphene oxide marked anti-aflatoxin B1 monoclonal antibody reaction reagent. The chromatographic test strip includes a cardboard; a water absorption pad, a detection pad and a sample pad are successively pasted on one side of the cardboard from top to bottom; adjacent pads are overlapped and connected at the junctions; the detection pad uses a nitrocellulose membrane as a base pad; the nitrocellulose membrane is provided with a horizontal quality control line and a test line from top to bottom; the quality control line is wrapped with rabbit antimouse polyclonal antibody; and the detection line is wrapped with an aflatoxin B1-bovine serum albumin conjugate (AFB1-BSA). The immunochromatographic test strip uses a carbon nano material as a marking material, which costs less than nano-gold and has high practical application value. The immunochromatographic test strip can be used for the detection of aflatoxin B1, and is easy to operate, simple and fast.