SARS-CoV-2 Antigen Rapid Test (Nasopharyngeal swab samples) SARS-CoV-2 Antigen Rapid Test Saliva) We have two fast screening reagents for routine detection. One is the antibody iggigm detection reagent (that is, blood for three minutes) One is antigen rapid screening test reagent (the same is three minutes can use nasal mucosa, oral mucosa, and saliva three detection methods) 1.SARS-CoV-2 antigen testing can detect infection earlier than antibody testing 2.SARS-CoV-2 antigen testing can detect SARS-CoV-2 and all mutant virus strains 3.Easy operation and quick results 4.The result is clear. C-line and T-line determines the infection and the result is easy to read 5.The colloidal gold method has stable performance and is not interfered by environmental and experimental conditions 6.Application: for human throat swab , nasal swab and sputum extract Our test kits for COVID-19 as below are still effective to detect the infection of new COVID-19 variant B.1.1.7and The new variant has no effect on the detection performance of products
Catalog Number: HSN01 Type: Point of Care Test Technical Details: Rapid antibody test kit made with blood sample Sample Types: Blood Plasma Sensitivity Rate: Sensitivity: 97%, Specifity: 97% Contents: Lancet, Pipette, Silica Gel, Alcohol Swab, Test cassette Number of Kits in a Box: 15 tests Storage Condition: Room Temperature Shipping Type: Shipping storage condition Room temperature Analysis Time: 15 Min < In short: In the IgG or IgM test line area, it reacts with locally bound anti-human IgG or IgM, respectively and forms a colored line. If sample does not contain any COVID-19 antibodies, a colored line showing a negative result will not appear in any of the Test Line Areas. As a positive check for the correct performance of the tape's procedure and operation, a colored line should always be appearing in the Control Line Area. If Control Line area is empty, then the test is invalid.
CTK BioTech's ' Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL, Higher accuracy, sensitivity and specificity than the Guaiac Test, No dietary restrictions, Clear, easy-to-interpret result, Individually sealed foil pouches containing: One cassette test device,, One desiccant, Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011), Patient ID stickers, One package insert (instruction for use).
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers 70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patient's visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 µL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use).
Product Details: Number of Reactions(Preps)/Kit : 25T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type :Rapid Test CAT No : R2011C Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL Higher accuracy, sensitivity and specificity than the Guaiac Test No dietary restrictions Clear, easy-to-interpret result Individually sealed foil pouches containing: One cassette test device One desiccant Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011) Patient ID stickers One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit ; 25T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type : Rapid Test CAT No : R0192C Clinical accuracy: 96.7% sensitivity, 93.8% specificity Analytical sensitivity: 100% positive detection rate at 1 ng/mL of pylori lysate antigen in fecal specimens Cross reactivity: no cross reactivity with the following organisms at â?¥ 1 x 108 org/mL: Acinetobacter calcoaceticus, Neisseria gonorrheae, Adenovirus, Neisseria meningitides, Enterococcus faecalis, Proteus mirabilis, Escherichia coli, Proteus vulgaris Hauser, Gardnerella vaginalis, Pseudomonas aeruginosa, Geotrichum candidum, Rotavirus, Haemophilus influenza, Salmonella Paratyphi A, �±-haemolytics streptococcus, Salmonella Paratyphi B, �²-haemolytic streptococcus, Salmonella Paratyphi C, Klebsiella pneumonia, Salmonella typhi, Moraxella catarrhalis Interference: No interference was seen with 5 mg/mL Tums�® Antacid, 1:20 Pepto-Bismol�® Antacid, 5 mg/mL Tagamet�® Antacid, 5% Barium sulfate, 5 mg/mL Prilosec Antacid, 12.5% Hemoglobin (tarry stool), or 1:20 Mylanta�® Antacid Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant Stool collection devices, each containing 2 mL extraction buffer Plastic droppers for transferring watery stool Package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit : 10 Brand : CTK BioTech Result Time (Rapid Kits): 15 min Sample Type : Blood Test Type Rapid Test CAT No : R0090C Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 aUL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit:10T Brand : CTK BioTech Result Time (Rapid Kits): 15 min Sample Type : Blood Test Type : Rapid Test CAT No : R0095C Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 AUL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use).
Product Details: Number of Reactions(Preps)/Kit : 10 Brand : CTK BioTech Result Time (Rapid Kits) : 20Min Sample Material ; Serum / Plasma / Whole Blood Cat. No : R0063c The OnSite Dengue Ag rapid Test CE is a lateral flow chromatographic immunoassay for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood. The test is designed to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with dengue virus. Any use or interpretation of this preliminary test result must also rely on other clinical findings and the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Recommended for use: Any person presenting with clinical signs or symptoms within 9 days consistent with acute dengue infection or dengue fever including: high fever, severe headaches, severe pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash. Dengue NS1 antigen is detectable in human blood from the first day after the onset of fever up to 9 days, which allows early detection and prompt treatment of infection with dengue virus. As mild dengue fever symptoms can overlap with acute clinical manifestations of other arbovirus infections, such as Zika virus and chikungunya virus infections, correct diagnosis of dengue infection during early disease onset is critical for guiding clinical patient management. Product Specification: Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (REF SB-R0063, 5 mL/bottle) One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit 10 T Brand CTK BioTech Test Type Rapid test Sample human serum, plasma, or whole blood Test time 10 Min Cat No : R0253C The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood. This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Recommended for use: Any person presenting with clinical signs or symptoms consistent with TORCH infection. Women who are pregnant or who are planning to become pregnant Individuals with a compromised immune system The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection. The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection. The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2. Product Specification : Individually sealed foil pouches containing: One cassette device Two desiccants Plastic droppers Sample diluent (REF SB-R0253, 5 mL/bottle) One package insert (instruction for use)
Product Details: Brand SD Country of Origin Made in India Specimen Serum Shelf Life 24 Months Temperature Storage 30 Degree Celsius Sensitivity 97.6% Specificity 98.0% H.Pylori Helicobacter pylori (H.pylori) is a spiral shaped bacterium and is found in the gastric mucous layer or adherent to epithelial lining of the stomach. H.pylori causes more than 90% of duodenal ulcers and up to 80% of gastric ulcers. Approximately two thirds of the world's population is infected with H.pylori. The immuno- chronomatographic techinques for the detection of antibodies specific to H.pylori has substantially resolved these problems. General Information: SD BIOLINE H.pylori test is a rapid test for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA etc) specific to Helicobacter pylori in human serum plasma or whole blood. Detection of all isotype (IgG, IgM, IgA) antibodies against H.pylori High Accuracy Sensitivity: 95.9%, Specificity: 89.6% Specimen: Serum. Plasma, Whole blood Material provided with this kit are as follows: SD BIOLINE H.pylori test device multi-device Assay diluent
Product Details: Number of Reactions(Preps)/Kit 40 Brand Abon Result Time (Rapid Kits) 15 mins The Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.
Igg Igm Antibody Rapid Test Kit.
Igg igm antibody rapid test kit.
Panodyne covid 19 antibody rapid test kit.
CTK Biotech's , The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7% Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes. Easily transported, and can be stored for 24 months at 2-30oC Individually sealed foil pouches containing: One cassette device One desiccant 5 µL capillary tubes Sample diluent (REF SB-R0092, 5 mL/bottle) Package insert (instruction for use)
Cat. No : ICO-3000. iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Cat. No : 9901-NCOV-01G. Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx. This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment.
CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood. Product Description Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity Differentiates Between Igg And Igm To Determine Stage Of Infection One Step Procedure Minimizes Operator Error Due To Sample Preparation High Level Of Reproducibility Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
