Canine Parvovirus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Parvovirus (CPV Ag) in dog's feces or vomit. Assay Time: 5 -10 min Sample: Feces or vomit Canine Parvovirus Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Parvovirus antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Canine Parvovirus antigen in the sample.
VETLabs Toxoplasma IgM/IgG test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for the rapid and qualitative detection of Toxoplasma IgM/IgG in cat's blood. The test device has a testing window, coated by an invisible T (test) zone and C (control) zone. When a sample is applied to the sample well on the device, the reagent will laterally flow on the surface of the test strip. If there is enough Toxoplasma IgM/IgG in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid test. By the means, the device can accurately indicate the presence of Toxoplasma IgM/IgG in the specimen. Kit components: 5 test per box and/or 10 test kit per box in an individual foil pouch with a desiccant and disposable dropper, EDTA blood collection tube, Assay buffer bottle, Instruction manual
VETlabs Canine Parvovirus (CPV) Ag/Canine Coronavirus (CCV) Ag Combo test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for the rapid and qualitative detection of Caine Parvovirus and Canine Coronavirus in dog's feces. The test device has a testing window, coated by an invisible T (test) zone and C (control) zone. When sample is applied into the sample well on the device, the reagent will laterally flow on the surface of the test strip. If there is enough CPV Ag/CCV Ag in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of CPV Ag/CCV Ag in the specimen.
Intended use: Toxoplasma IGG/IGM rapid test is a rapid immunochromatographic test for the simultaneous detection of IGM and IGG antibodies to toxoplasma gondii in human serum/plasma. The test can be used as a screening test for toxoplasma infection and as an aid for differential diagnosis of the self limiting primary toxoplasma infections and the potentially fatal secondary toxoplasma infections in conjunction with other criteria. Test principle: The toxoplasma IGG/IGM rapid test is a lateral flow chromatographic immunoassay. The test cassette consists of: 1) A burgundy colored conjugate pad containing toxoplasma recombinant envelope antigens conjugated with colloid gold (toxoplasma conjugates) and rabbit igg-gold conjugates, 2) A nitrocellulose membrane strip containing two test bands (t1 and t2 bands) and a control band (c band). The t1 band is pre-coated with the antibody for the detection of IGM anti-toxoplasma, t2 band is coated with antibody for the detection of igg anti-toxoplasma, and the c band is pre-coated with goat anti rabbit IGG. Absence of any t bands (t1 and t2) suggests a negative result. The test contains an internal control (c band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit igg/rabbit igg-gold conjugate regardless of the color development on any of the t bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Reagents and materials supplied : 1. Test cassette individually foil pouched with a desiccant. 2. Plastic dropper 3. Buffer 4. Package insert. Storage and stability: The kit must be stored at 2-30pc. Warning and precautions: 1. For in vitro diagnostic use only. Not for medicinal use. 2. Do not use beyond expiry date. 3. Read the instructions careful y before performing the test. 4. Handle all specimen as potential y infectious. 5. Follow standard biosafety guidelines for handling and disposal of potential y infective material.
SARS-CoV-19 IgG/IgM test kit (15min showing result) Manufacturer: Guangzhou Wanfo Biotech Co., Ltd. a China listing company Certificates: CE certificate, China NMPA approval (export allowed), no FDA approval The price is $5.5/test (FOB) Max delivered quantity: 100,000/weekly More details please enquire Barry Liu whatsapp: +8617810331113 sample available: 20 test & DHL delivery: $200 Download introductions: https://kdocs.cn/l/sLLC9O6rc
VETlabs Peritonitis Detection Kit, which is developed and manufactured by Bioguard Corporation, can differentiate a transudate from an exudate. When the exudate contains reaction-positive proteins, it forms an effusion drop, which precipitates in the reaction solution. The formation of precipitated products, teardrop-shaped, mists or smears can be observed during the test. In contrast, the transudate will completely dissolve in the reaction solution during the sedimentation. Each box contains 6 test kits including 6 reaction tubes with acetic acid solution, 6 droppers, 6 dye-containing tubes and an instruction manual.
VETlabs Feline Panleukopenia Viraus (FPV) Ag Test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for rapid and qualitative detection of Feline Panleukopenia Virus in cat's feces or vomit.
Canine Influenza Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Influenza virus (CIV Ag) in dog's secretions. Assay Time: 5 -10 min Sample: Secretions Canine Influenza Virus Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When a sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Influenza antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Canine Influenza antigen in the sample.
Canine Adenovirus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Adenovirus (CAV Ag) in dog's secretions or serum.. Assay Time: 5 - 10 min Sample: Secretions or serum Canine Adenovirus Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Adenovirus-II antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Canine Adenovirus-II antigen in the sample.
Canine Coronavirus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Canine Coronavirus (CCV Ag) in dog's feces or vomit. Assay Time: 5 -10 min. Sample: Feces or vomit. Canine Coronavirus Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Coronavirus antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Canine Coronavirus antigen in the sample.
Feline Coronavirus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Coronavirus antibody (FCoV Ab) in cat's blood. Assay Time: 5-10 mins Sample: serum, plasma or blood Feline Coronavirus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FCoV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Feline Coronavirus antibody in the sample.
It's special designed to detect the Aflatoxin M1 in raw, commingled cow milk at or below established tolerance and/or safe levels. The kit is only for screening test, positive result should be further confirmed with other method.
H-fabp fast test kit (immunofluorescence assay) is intended for use together with getein1100 immunofluorescence quantitative analyzer (getein1100) or getein1600 immunofluorescence quantitative analyzer (getein1600) to quantitatively determine the concentrations of h-fabp in human serum, plasma, or whole blood specimens in point-of care and laboratory settings. H-fabp fast test kit (immunofluorescence assay) is intended for in vitro quantitative determination of heart-type fatty acid binding protein (h-fabp) in serum, plasma or whole blood. This test is used in the early diagnosis of ami and pulmonary embolism, and monitoring of chronic heart failure.
The cardiac troponin i fast test kit (colloidal gold) is intended for use together with the fia8000 quantitative immunoassay analyzer (fia8000). The product employs colloidal gold immunochromatogrphy to determine ctni in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify ctni specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of ctni. Then insert test card into the fia8000 quantitative immunoassay analyzer, the concentration of ctni is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for NT-proBNP (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NT-proBNP in human serum, plasma, or whole blood specimens. One monoclonal antibody and one polyclonal antibody are employed to identify NT-proBNP specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NT-proBNP. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NT-proBNP is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for PCT (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine PCT in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify PCT specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of PCT. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of PCT is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for NAGL (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NGAL in human urine specimen. Monoclonal antibody and polyclonal antibody are employed to identify NGAL specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NGAL. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NGAL is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for B2-MG (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine B2-MG in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify B2-MG specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of B2-MG. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of B2-MG is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for mAlb (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine mAlb in human urine specimen. Polyclonal antibody and recombinant antigen are employed to identify mAlb specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of mAlb. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of mAlb is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
In the past two months, China was infected by the COVID-19( Noval Coronavirus), in order to diagnose the diseases earlier, Encode team work hard and finally develop the COVID-19 IgM/IgG rapid test kit, which clinical positive detection rate is over 90%.
