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.
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 can be used for rapid screening of carriers of the virus that are symptomatic or asymptomatic. Recent studies suggest that a high percentage of patients show no clinical symptoms of the virus, thus screening patients is vitally important. The test is ideally suited for hospitals, clinics and test laboratories.
Rapid SAR-CoV-2 (Covid-19) Test Kits: FDA & CE Approved (Results in 15 min). SAR-CoV-2 IgG/IgM Rapid Test Cassette is a qualitative membrane based immunoassay for the detection of IgG and IgM antibodies to SAR-CoV-2 in human whole blood, serum or plasma specimen. Made in China: FDA and CE Approved, China NMPA approval (export allowed) One of the earliest CE (Feb 2020) and FDA (Mar 2020) approved kit. Clinically studied and reliable. Packaging: 20 sets/box or 40 sets/box. Payment term: MOQ 2000 sets, FOB China $ 9.5/set. < 10000 sets 100% advance payment > 10000 sets L/C ex-work on site
1. Principle This kit is based on the specific reaction of antibody-antigen and immunochromatography. β-lactam and tetracyclines antibiotics in the sample compete for the antibody with the antigen coated on the membrane of the test strip. Then after a color reaction, the result can be observed. 2. Applications This kit is used for rapid qualitative analysis of β-lactam and tetracyclines in milk sample.
Pcr test kit, n95 , nitrile gloves, face shields.
Pcr (polymerase chain reaction) instrument, thermal cycler, nucleic acid extraction instrument, thermal mixer, thermal shaker, dry bath (cooling or heating), pcr detection kit, covid 19 test, pcr kit for human disease, pcr kit for animal disease, plastic consumables like tip, dishes, flasks..
Covid Test Kits, Cancer Diagnostic Device / Kits(for Human And For Animal), Various Disinfection Products.
Iir Mask, 3 Ply Masks Level 1, Medical Grade Gloves, Otc Antigen Test Kits, Rapid Pcr Tests.
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.
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.
