General Information One-Step Adenovirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of adenovirus in human fecal specimens. Sensitivity: 98.7% , Specificity: 98.0% Detection limit:1.37s/CO Specimen: Feces Reading Time : 10min
General Information One-Step Rotavirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of rotavirus in human fecal specimens. Sensitivity: 99.1% , Specificity: 99.9% Detection limit:103.5TCID50/ml Specimen: Feces Reading Time : 10min
General Information One-Step H.Pylori Ag Rapid Test is to detect the antigens in stool. For H.Pylori Ag Rapid tests: Sensitivity: 98.9 %, Specificity: 98.5%, Specimen: Stool Reading Time: 10 min
General Information One-Step H.Pylori Ab Rapid Test is to detect the antibodies against H. pylori in serum, plasma or whole blood. For H.Pylori Ab Rapid tests: Sensitivity: 98.9 %, Specificity: 98.5%, Specimen: Serum, Plasma or Whole Blood Reading Time: 10 min
General Information One-Step Dengue Rapid Test is to detect the NS1 antigens and IgG&IgM antibodies in human blood. Sensitivity : 99.9% Specificity : 99.5 % Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
General Information The CRP Semi-Quantitative Rapid Test utilizes a combination of colloidal gold conjugate and anti-CRP antibodies to selectively detect CRP in human blood. Sensitivity:97% , Specificity:96.9% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 -15min
General Information One-Step Cow Ovulation Rapid Test is to detect the Beta-LH in milk. Analytical sensitivity : 10mIU/ml Sensitivity : 90% , Specificity : 90% Specimen : Milk Reading Time : 5 min No cross-reactivity: FSH (500ng/mL), Beta-E2(500ng/mL), PRL(500ng/mL), ASA(20µg/mL), DHT(20¼g/mL), tetraborane(20g/mL) and 0.01nol/mL pH 7.3 PBS
General Information One-Step FOB Rapid Test is qualitative test for the detection of human blood hemoglobin in human stool specimens and early diagnosis for Colon Cancer by Fecal Occult Blood screening with double methods, immunology and chemistry No Cross reactivity :(Bovine, Hemoglobin, Swine hemoglobin, Horse hemoglobin, Bililrubin, Bovine serum albumin, Vitamin C) Analytical sensitivity : 20ng/ml of FOB (immunology) ,100ng/ml of FOB (chemistry) Specimen : Stool
General Information One-Step the D-Dimer Rapid Test Device is a chromatographic immunoassay for the qualitative detection of D-Dimer in human blood. Specimen : Serum, Plasma or Whole Blood Reading Time : 10 -15min
General Information The CRP C-Reactive Protein Semi-Quantitative Rapid Test utilizes a combination of colloidal gold conjugate and anti-CRP antibodies to selectively detect CRP in human blood. Sensitivity:97% , Specificity:96.9% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 -15min
General Information Method: Double Antibodies Sandwich Method Sensitivity : 99.8% Specificity : 99.6% Specimen : Canine feces or vomit Detection limit: 103 TCID50 / mL No cross reaction against CDV, CCV, CRV, CAV - I, Giardia Reading Time : 5- 10 min
General Information One-Step Canine Influenza Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Influenza virus (CIV Ag) in dog secretions. Sensitivity: 94.7% , Specificity: 100% Specimen: Secretions Reading Timen:5-10 min
The Cytomegalovirus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of Cytomegalovirus (CMV) in human serum/plasma samples. Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients. The Cytomegalovirus Rapid Test Device (Serum/Plasma) has been designed to detect CMV through visual interpretation of color development in the internal strip. The membrane was immobilized with antigens of CMV on the test region. During the test, the specimen is allowed to react with colored recombinant mouse anti-human IgM latex conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough CMV antibodies in specimens, a colored band will from at the test region of the membrane. Presence of this colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.
General Information One-Step Chloramphenicol Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Chloramphenicol residue in milk, Honey,Tissue extract and Aquatic products. Detection limit: Milk 0.3ppb ,Honey 0.3ppb , Tissue extract 0.3ppb , Aquatic products 0.3ppb Specimen: Defatted milk, Honey, Tissue extract, Aquatic products Reading Time : 5-10min
General Information One-Step Streptomycin Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Streptomycin residue in milk,honey and aquatic product . Detection limit:Milk 100ppb , Honey 10ppb , Aquatic product 100ppb Specimen: Defatted Milk, Honey,Aquatic products Reading Time : 5-10 min
General Information One-Step Sulfonamides Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Sulfonamides residue in Milk,Honey,Tissue extract and Aquatic products. Specimen: Milk, Honey, Tissue extract, Aquatic products Reading Time : 5-10 min
Uncut Sheet Strep A IgG/IgM Rapid Test Format:Cassette/Strip Uncut Sheet A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only. INTENDED USE The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection. SUMMARY Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4 The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen. PRINCIPLE The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
Uncut Sheet Influenza A/B Rapid Test Specimen:nasal swab Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30 or 40-86). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
INTENDED USE The Helicobacter-Pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of H. pylori infection. INTRODUCTION Helicobacter pylori (also known as Campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma. The epidemiologic study shows that more than 50% of the world's population is infected by H. pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by H. pylori strains. So the detection and treatment of H. pylori strains infection is very important. At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical ELISA and immunoblot assays. This Kit belongs to non-invasive approach.
INTENDED USE 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 25 PCS/BOX
