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74 results about "IgM.monoclonal" patented technology

Novel fluorescence immunochromatography test strip for joint inspection of SARS-CoV-2 IgG-IgM antibodies of coronaviruses

The invention discloses a novel fluorescence immunochromatography test strip for joint inspection of SARS-CoV-2 IgG-IgM antibodies of coronaviruses. The test strip comprises a bottom plate, a sample pad, a combination pad, a nitrocellulose membrane and a water absorption pad, wherein the sample pad, the combination pad, the nitrocellulose membrane and the water absorption pad are sequentially connected end to end and adhered to the bottom plate; the combination pad is coated with an SARS-CoV-2 structural protein-marker and a goat anti-rabbit IgG-marker, and the nitrocellulose membrane is provided with a detection line T1 coated with a mouse anti-human IgG monoclonal antibody, a detection line T2 coated with a mouse anti-human IgM monoclonal antibody and a quality control line C coated withrabbit IgG. When the test strip is used for quantitatively detecting SARS-CoV-2 IgG and IgM antibodies, the detection sensitivity is high, and the specificity is good and can reach 96%; the batch-to-batch difference is small, and good repeatability is achieved; the test strip can be stored for half a year at normal temperature without reducing the sensitivity and has good stability; the test strip is simple to operate and low in cost, can quickly and quantitatively detect the levels of SARS-CoV-2 IgG and IgM antibodies in a human body, assists a nucleic acid detection means, and provides powerful support for epidemic situations.
Owner:NANJING AGRICULTURAL UNIVERSITY

Detection reagent of treponema pallidum IgM (Immunoglobulin M) antigen colloidal gold method and preparation method thereof

The invention discloses a detection reagent of a treponema pallidum IgM (Immunoglobulin M) antigen colloidal gold method and a preparation method thereof. The reagent comprises a gold conjugate pad (3), a cellulose nitrate reaction membrane (4), a sample pad (2), water absorbing paper (5) and a PVC (Polyvinyl Chloride) back lining (1), wherein the sample pad, the gold conjugate pad, the cellulose nitrate reaction membrane and the water absorbing paper are sequentially and mutually laminated and adhered on the PVC back lining; the sample pad is laminated on the gold conjugate pad for 2-3 mm, the gold conjugate pad is laminated on the cellulose nitrate reaction membrane for 2-3 mm, and the water absorbing paper is laminated on the cellulose nitrate reaction membrane for 2-3 mm; the gold conjugate pad is coated with an anti-human IgM monoclonal antibody-colloidal gold conjugate; and positions of a quality control region (7) and a detection region (6) of the cellulose nitrate reaction membrane are coated with goat anti-mouse IgG antibody or rabbit anti-mouse IgG antibody and specific gene recombinant treponema pallidum antigen respectively. A production process of a product provided by the invention is simple and easy to control; the detection reagent is easy, convenient and quick in detection; and a result can be read in 25 minutes and is not affected by the IgG antibody and is accurate and reliable.
Owner:BEIJING BIONEOVAN

Mycoplasma pneumoniae IgM antibody colloid gold method detecting kit and preparation method thereof

InactiveCN102305856AObvious detectabilityReduce the effectMaterial analysisPaper tapeMurine antibody
The invention relates to a mycoplasma pneumoniae IgM antibody colloid gold method detecting kit which comprises a nitrocellulose membrane detecting line coated recombinant antigen MP-Ag, a quality control line coated goat anti-mouse IgG antibody and a gold labeled pad coated mouse anti-human IgM monoclonal antibody which is marked by colloidal gold, wherein the recombinant mycoplasma pneumoniae antigen is colorless transparent liquid, has the concentration of larger than 2mg/ml and is detected by SDS-PAG; the goat anti-mouse IgG antibody is colorless transparent liquid and has the concentration of larger than 4mg/ml; the mouse anti-human IgM monoclonal antibody is colorless transparent liquid, has the concentration of larger than 2mg/ml and is detected by SDS-PAGE; and the sample loading amount uses two strips under the condition of 10 microliters. The mycoplasma pneumoniae IgM antibody colloid gold rapid detecting test paper tape uses multiepitope recombinant antigen as a raw materials, has the characteristics of simpler operation, low cost, high specificity and high sensitivity, can carry out single detection, is easy for popularization and has obvious detecting and control effect on the mycoplasma pneumoniae IgM antibody.
Owner:北京中检安泰诊断科技有限公司

Porcine pseudorabies virus gE IgM antibody colloidal gold immunochromatograohic assay test strip as well as preparation method and application thereof

The invention discloses a porcine pseudorabies virus gE IgM antibody colloidal gold immunochromatograohic assay test strip as well as a preparation method and application thereof. The test strip comprises a sample absorption region, a colloidal gold labeled probe region, a solidifying antibody region, a water absorption region, a bottom plate and a clamping shell, wherein the sample absorption region, the colloidal gold labeled probe region, the solidifying antibody region and the water absorption region are sequentially bonded on the bottom plate and are interlapped in the clamping shell; the sample absorption region is coated with purified porcine pseudorabies virus gE protein; the colloidal gold labeled probe region is coated with colloidal gold labeled porcine pseudorabies virus gE protein monoclonal antibody; the solidifying antibody region is sequentially provided with a detection line T coated with mouse anti-pig IgM monoclonal antibody and a control line C coated with goat anti-mouse IgG. The test strip is simple to operate, good in repeatability, high in sensitivity, rapid and intuitive in result, simple in process and low in cost, can be mass-prepared, and is suitable for mass field test and early diagnosis for porcine pseudorabies virus infection in swinery.
Owner:WUHAN CHOPPER BIOLOGY

Chlamydia pneumoniae IgM (immunoglobulin M) colloidal golden method kit and preparation method thereof

InactiveCN102749446AObvious detectabilityReduce the effectMaterial analysisMurine antibodyChlamydiae
The invention discloses a chlamydia pneumoniae IgM (immunoglobulin M) colloidal golden method kit which comprises recombinant chlamydia pneumoniae antigens enveloped on a nitrocellulose membrane detection line, goat anti-rat IgG (immunoglobulin G) antibodies enveloped on a quality control line and rat anti-human IgM monoclonal antibodies which have colloidal gold labels and are enveloped on a gold label pad, the concentration of the chlamydia pneumoniae antigens ranges from 1mg/ml to 2mg/ml and is measured by SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis), the concentration of the goat anti-rat IgG (immunoglobulin G) antibodies ranges from 1mg/ml to 3mg/ml, and the concentration of the rat anti-human IgM monoclonal antibodies ranges from 5g/mL to 30g/mL and is measured by the SDS-PAGE. The chlamydia pneumoniae IgM colloidal golden method kit has the advantages that the kid is speedy, simple, convenient and accurate and is high in sensitivity, and a judgment result can be read after integral operation time of dozens of minutes; and a colloidal gold quick detecting paper strip is made of the multi-epitope recombinant antigens and is simple and convenient to operate, low in cost, good in specificity and high in sensitivity, can be used for single-component detection and is popularized easily, and detection and control effects for chlamydia pneumoniae IgM are obvious.
Owner:北京中检安泰诊断科技有限公司

Preparation method of respiratory syncytial virus antigen and rapid respiratory syncytial virus antibody detection kit prepared from antigen

The invention relates to a respiratory syncytial virus antigen for diagnosing respiratory syncytial virus infection, a method for preparing the antigen, a method and a reagent for detecting respiratory syncytial virus infection by using the antigen, and belongs to the field of clinical medical detection. The artificially synthesized optimized respiratory syncytial virus F1 gene was constructed as a prokaryotic expression vector, and Escherichia coli was used to express the respiratory syncytial virus F1 antigen, and inclusion bodies with three-dimensional structure and immunity were obtained by renaturation by dialysis, gradient dilution and gel chromatography. Active recombinant respiratory syncytial virus F1 protein antigen. The present invention applies colloidal gold immunochromatography technology, uses engineered expressed respiratory syncytial virus F1 antigen as detection antigen, uses high-efficiency anti-human IgG or IgM monoclonal antibody as capture antibody, and filters red blood cells with blood filter membrane, according to "indirect method" The principle is to prepare a rapid detection kit for respiratory syncytial virus antibody, which is used to detect respiratory syncytial virus antibody in human serum, plasma or whole blood. It has the advantages of simple detection method, accurate and rapid result display, and no need for special equipment.
Owner:LANZHOU YAHUA BIOTECH

A colloidal gold method detection kit for hepatitis A virus igm antibody and preparation method thereof

The invention discloses a colloidal gold detection kit for hepatitis A virus IgM antibody, comprising a recombinant antigen HAV-Ag coated on a nitrocellulose membrane detection line, a goat anti-mouse IgG antibody and a gold label coated on a quality control line The mouse anti-human IgM monoclonal antibody labeled with colloidal gold coated on the pad, the recombinant hepatitis A virus antigen concentration was greater than 2mg / ml, and was determined by SDS-PAGE; the goat anti-mouse IgG antibody concentration was greater than 4mg / ml; The concentration of the mouse anti-human IgM monoclonal antibody was greater than 2 mg / ml, which was determined by SDS-PAGE, and the loading amount was two bands under the condition of 10 μl. The beneficial effects of the invention are as follows: the hepatitis A virus IgM antibody detection kit has the characteristics of rapidity, simplicity, accuracy and high sensitivity, and the whole operation time only takes 20 minutes to interpret the results. The colloidal gold rapid detection test strip is based on the multi-epitope recombinant antigen as the raw material. It has the characteristics of easier operation, low cost, good specificity and high sensitivity. It can be detected in a single batch and is easy to popularize. The detection and control effect is obvious.
Owner:北京中检安泰诊断科技有限公司

EB virus capsid antigen IgM antibody colloidal gold method detection reagent and preparation method thereof

The present invention discloses an EB virus capsid antigen IgM antibody colloidal gold method detection reagent and a preparation method thereof. The reagent comprises a gold conjugate pad (3), a nitrocellulose reaction membrane (4), a sample pad (2), a rheumatoid factor treatment pad (1), water absorption paper (5) and a PVC backing (8), wherein a length of the rheumatoid factor treatment pad is approximately 1/2 of a length of the sample pad, the sample pad, the gold conjugate pad, the nitrocellulose reaction membrane and the water absorption paper are sequentially and mutually laminated and adhered on the PVC backing, the gold conjugate pad is coated with an anti-human IgM monoclonal antibody-colloidal gold conjugate, and positions of a quality control area (7) and a detection area (6) of the nitrocellulose reaction membrane are respectively coated with goat anti-mouse IgG antibody or rabbit anti-mouse IgG antibody and specific gene recombinant EB virus capsid antigen. According to the present invention, a production process is simple and easy to control, test results can be obtained within 25 minutes, self-detection can be achieved according to operations in a manufacturer's instruction, test results are not affected by the rheumatoid factor, sensitivity is high, specificity is good, and results are accurate and reliable.
Owner:BEIJING BIONEOVAN

Dengue fever NS1 antigen and IgG/IgM antibody two-joint inspection test strip, detection card and kit

The invention relates to a dengue fever NS1 antigen and IgG/IgM antibody two-joint inspection test strip, which comprises a dengue fever NS1 antigen test strip and a dengue fever IgG/IgM antibody teststrip, and is characterized in that the dengue fever NS1 antigen test strip comprises a first gold labeled pad layer and a first nitrocellulose membrane, and the first gold labeled pad layer is immobilized with a dengue fever NS1 monoclonal antibody colloidal gold compound; and the first nitrocellulose membrane is coated with detection lines of four serotypes of dengue fever NS1 monoclonal antibodies, the dengue fever IgG/IgM antibody test strip comprises a second gold labeled pad layer and a second nitrocellulose membrane, and the second gold labeled pad layer is immobilized with four serotypes of dengue fever recombinant antigen colloidal gold compounds. The second nitrocellulose membrane is coated with a detection line T1 of a mouse anti-human IgG monoclonal antibody and a detection line T2 of a mouse anti-human IgM monoclonal antibody; and according to the test strip, IgM/IgG antibodies and NS1 antigens can be jointly detected through one-time operation, the operation process is simplified, the immune response reaction state of an organism is effectively diagnosed, and the purpose of real POCT detection is achieved.
Owner:山东康华生物医疗科技股份有限公司

Porcine circovirus type 2 (PCV2) IgM antibody colloidal gold immunochromatographic assay test paper, and preparation method and application thereof

InactiveCN103969451AOvercome the disadvantage of low sensitivityImprove featuresBiological testingCircovirusProtein.monoclonal
The invention discloses a porcine circovirus type 2 (PCV2) IgM antibody colloidal gold immunochromatographic assay test paper, and a preparation method and application thereof. The test paper comprises a sample absorption region, a colloidal gold labeled probe region, a curing antibody region, a water absorption region, a backboard and a shell, wherein the sample absorption region, colloidal gold labeled probe region, curing antibody region and water absorption region are sequentially attached to the backboard and arranged in the shell in a superposition mode. A purified PCV2 Cap protein is coated on the sample absorption region; a colloidal gold labeled PCV2 Cap protein monoclonal antibody is coated on the colloidal gold labeled probe region; and the curing antibody region is sequentially provided with a detection line T coated mouse anti-pig IgM monoclonal antibody and a control line C coated goat anti-mouse IgG. The test paper is simple to operate, has the advantages of favorable repetitiveness, high sensitivity, quick and visual results, simple technique and low cost, can implement mass preparation, is suitable for mass field detection for basic level, and can be used for early quick diagnosis on swinery PCV infections.
Owner:WUHAN CHOPPER BIOLOGY
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