Rapid Anti-CSFV Test FOR THE DETECTION OF CSFV ANTIBODY IN SWINE SERUM, PLASMA OR WHOLE BLOOD Catalog Number: 9002 INTENDED USE Rapid anti-CSFV (Classical swine fever Virus) Test is a chromatographic immunoassay for detection of the antibody against the Classical swine fever Virus in swine. SUMMARY AND EXPLANATION Rapid Anti-CSFV Test employs chromatographic lateral flow device for detection of the Classical swine fever antibody in samples ( serum, plasma or whole blood ). Colloidal gold conjugated with inactive Classical swine fever (CSF) antigen (Au-Ag1) are prior dry-immobilized onto a fiberglass paper. On nitrocellulose membrane, CSF antigen (Ag2) is coated in the Test Zone (T) and Rabbit anti-CSF Ab is coated in the Control Zone (C) . When the sample is added, it migrates by capillary diffusion through the strip rehydrating the gold conjugate. If present, CSF antibody in sample will bind with the gold conjugated Au-Ag1 forming particles. These particles will contin

Rapid CSFV Test FOR THE DETECTION OF CSFV ANTIGEN IN SWINES SERUM, PLASMA OR WHOLE BLOOD Catalog Number: 9001 INTENDED USE Rapid CSFV (Classical swine fever virus) Test is a chromatographic immunoassay for detection of the Classical swine fever virus antigen in swines (serum, plasma or whole blood). It is used to assistant diagnosis of CSF. SUMMARY AND EXPLANATION Rapid CSFV Test employs chromatographic lateral flow device for detection of the Classical swine fever antigen in samples ( serum, plasma or whole blood ). Colloidal gold conjugated with Mouse anti-CSFV MAb (Monoclone) (Au-Ab1) are prior dry-immobilized onto a fiberglass paper. On nitrocellulose membrane, Mouse anti-CSFV MAb (Ab2) is coated at Test Zone (T) and Goat anti-mouse IgG is coated at Control Zone (C) . When the sample is added, it migrates by capillary diffusion trough the strip rehydrating the gold conjugate. If present, CSF antigen (Ag) in sample will bind with the gold conjugated Au-Ab1 forming part

RAPID MYOGLOBIN TEST CARD FOR THE QUALITATIVE ASSESSMENT OF HUMAN MYOGLOBIN IN HUMAN SERUM AND PLASMA Catalog Number: 75005 For in vitro Diagnostic Use INTENDED USE Rapid Myoglobin test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of myoglobin in human serum specimens. The presence of myoglobin in serum or plasma specimens at level 100 ng/ml or higher can be detected in 10 minutes. SUMMARY AND EXPLANATION Myoglobin is a low molecular weight, cytoplasmic serum protein. Due to its low molecular weight, myoglobin is released more rapidly when muscle cells are damaged than other markers. Serum concentration of myoglobin increases above the normal range as early as 1 hour after myocardial infarction, and peak in approximately 4 to 8 hours after onset. Therefore, myoglobin is better suited for the early diagnosis of

CK-MB SERUM TEST FOR THE QUANTITATIVE ASSESSMENT OF HUMAN CK-MB IN HUMAN SERUM Catalog Number: 75003 For in vitro Diagnostic Use INTENDED USE Rapid CK-MB test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of CK-MB in human serum specimens as an aid in the diagnosis of myocardial infarction. SUMMARY AND EXPLANATION Creatine kinase is a dimer occurring in various in three isoenzymic forms, depending on the particular combination of its non-identical subunits:BB(brain type);MM(skeletal type); and MB(hybrid type). Creatine kinase-MB isoenzyme is released into circulation later than myoglubin, reaching abnormal levels within 4 to 6 hours after onset of symptoms,it reaches its highest level with a typical range of 39-185 ng/ml after about 18 to 24 hours,and returns to normal in about 2 to 3 days.CK-MB is w

TROPONIN I TEST CARD FOR THE QUALITATIVE ASSESSMENT OF CARDIAC TROPONIN I IN HUMAN SERUM OR PLASMA Catalog Number: 75001 For in vitro Diagnostic Use INTENDED USE Rapid TnI test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of cardiac troponin I (cTnI) in human serum or plasma specimens as an aid in the diagnosis of myocardial infarction. SUMMARY AND EXPLANATION Cardiac troponin I (cTnI) is a cardiac muscle protein with a molecular weight of 22.5 kilodaltons. Together with troponin T (TnT) and troponin C (TnC), TnI forms a troponin complex in heart to play a fundamental role in the transmission of intracellular calcium signal actin-myosin interaction. The human cTnI has an additional amino acid residues on its N-terminal that are not exis

Rapid PSA TEST FOR THE SEMI-QUANTITATIVE ASSESSMENT OF HUMAN PSA IN HUMAN SERUM AND PLASMA Catalog Number: 72003 For in vitro Diagnostic Use INTENDED USE Rapid PSA Test is an immunochromatography based one step in vitro test. It is designed for the rapid semi-quantitative determination of human prostate specific antigen (PSA) in serum or plasma specimens. SUMMARY AND EXPLANATION Prostate cancer is the one of the most common types of cancer found in man. The incidence of prostate cancer increases with age and accounts for a growing number of newly diagnosed patients. Prostate specific antigen (PSA) is produced primarily in the prostate gland and is secreted into the prostate ducts and at ejaculation serves to liquefy the seminal coagulum. Virtually all healthy males under 50 years of age have PSA concentration under 4.0 ng/ml. If PSA level is above 20 ng/ml, the patient most likely to have prostate cancer. Some studies indi

FECAL OCCULT BLOOD TEST CARD FOR THE QUALITATIVE ASSESSMENT OF HUMAN HEMOGLOBIN IN FECES Catalog No.: 07RD-7055 For In-Vitro Diagnostic Use INTENDED USE The Fecal Occult Blood test is a qualitative test that detects human hemoglobin in human fecal specimens. The test is a visual one step, in-vitro assay. It is intended for professional use to help diagnose gastrointestinal bleeding. SUMMARY AND EXPLANATION Colorectal cancer is the third most common cancer in the world. “Fecal occult blood” is generally defined as a blood loss of less than 50 mL/d. The appearance of occult blood in human fecal specimen is often associated with gastrointestinal diseases which might cause colorectal cancer if not treated promptly and properly. The traditional guaiac-based method lacks sensitivity and specificity, and has diet restrictions prior to the testing. The Fecal Occult Blood Test uses

RAPID ADENO-ROTA VIRUS ANTIGEN COMBO TEST Cat.# 71033 Immunochromatographic rapid assay for the Detection of Adenovirus and Rotavirus Antigens in Human Stool Specimens INTENDED USE Rapid Adeno/Rota Combo Test is an in vitro qualitative immunochromatographic assay for the rapid detection of adenovirus rotavirus antigens in human stool specimen. The test results are intended to aid in the diagnosis of rotavirus infection and to monitor the effectiveness of therapeutic treatment. PRINCIPLE OF THE TEST Rapid Adeno/Rota Combo Test is a sandwich solid phase immunochromatographic assay. To perform the test, an aliquot of diluted stool sample is added to the sample well of the test cassette. The sample flows through a pad containing antibodies against adenovirus and rotavirus coupled to red-colored colloidal gold. If the sample contains adenovirus or rotavirus antigens, the antigen will bind to the antibody coated on the colloidal gold particles to form antigen-antibody-go

RAPID HELICOBACTER PYLORI ANTIGEN TEST Cat.# 71020 Immunochromatographic rapid assay for the Detection of Helicobacter pylori Antigens in Human Stool Specimens INTENDED USE Rapid H. pylori Antigen Test is an in vitro qualitative immunochromatographic assay for the rapid detection of Helicobacter pylori antigens in human stool specimen. The test results are intended to aid in the diagnosis of H. pylori infection, to monitor the effectiveness of therapeutic treatment and to confirm the eradication of H. pylori in peptic ulcer patients. PRINCIPLE OF THE TEST Rapid H. pylori Antigen Test is a sandwich solid phase immunochromatographic assay. To perform the test, an aliquot of diluted stool sample is added to the sample well of the test cassette. The sample flows through a label pad containing H. pylori antibody coupled to red-colored colloidal gold. If the sample contains H. pylori antigens, the antigen will bind to the antibody coated on the colloidal gold particles t

RAPID H. PYLORI ANTIBODY TEST Cat.# 71024 A Rapid qualitative Immunochromatographic test for the detection of antibodies against H. Pylori in human Whole Blood, Serum or plasma INTENDED USE Rapid H. Pylori Antibody Test is a rapid immunochromatographic assay for the detection of antibodies to H. pylori in human whole blood, serum or plasma. The assay is to provide an aid in diagnosis of H. pylori infection. TEST PRINCIPLE Rapid H. Pylori Antibody Test employs chromatographic lateral flow test device in a cassette format. Colloidal gold conjugated H. pylori antigens (Au-Ag) are dry-immobilized at the end of nitrocellulose membrane strip. H. Pylori antigens are bond at the Test Zone (T) When the sample is added, it migrates by capillary diffusion rehydrating the gold conjugate. If anti-H. pylori antibodies present in sample, Antibodies will bind with the gold conjugated antigens forming particles. These particles will continue to migrate along the strip until the Tes

Rapid Dengue IgG/IgM Combo Test Cat.# 71019 A Rapid qualitative Immunochromatographic test for the simultaneous detection of IgG and IgM Antibodies to Dengue Virus in human Whole Blood, Serum or plasma INTENDED USE Rapid Dengue Test is a rapid immunochromatographic assay for the simultaneous detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum or plasma. The assay is used as a screening test for Dengue viral infection and as an aid for differential diagnosis of primary and secondary infections in conjunction with other criteria. TEST PRINCIPLE Rapid Dengue Test utilizes the principle of Immunochromatography. Mouse anti-human IgM and human IgG antibodies are immobilized on the nitrocellulose membrane respectively, as two individual test lines (IgM line and IgG line) in the test window of the test device. The IgG line in the test window is closer to the sample well and followed by IgM line. As the test sample flows through the membrane ass

RAPID HIV I&II TEST CARD FOR THE QUALITATIVE ASSESSMENT OF HIV I&II ANTIBODIES IN HUMAN SERUM, WHOLE BLOOD OR PLASMA Catalog Number: 71002 For in vitro Diagnostic Use Only INTENDED USE Rapid HIV 1&II test is a single use, rapid device intended for qualitative detection of antibodies to Human Immunodeficiency Viruses or HIV(1+2) in whole blood samples. It is intended for use in medical institution as the aid for the diagnosis of possible HIV infection and for the quick screening of blood donors and blood products. PRINCIPLE OF THE ASSAY This test employs chromatographic lateral flow device in a cassette format.Colloidal gold conjugated recombinant antigens (Au-Ag) corresponding to HIV-1 gp120, gp41 and HIV-2 gp-36 are dry-immobilized at the end of nitrocellulose membrane strip. HI

RAPID HCV ANTIBODY TEST FOR THE QUALITATIVE ASSESSMENT OF HCV ANTIBODY IN HUMAN SERUM, OR PLASMA Catalog Number: 71030 INTENDED USE Rapid HCV Ab Test is a chromatographic immunoassay for qualitative detection of the antibodies against hepatitis C virus (HCV Ab) in human serum and plasma samples. It is intended for use in medical institution as an aid for diagnosis and management of patients related to infection with hepatitis C as well for primary screening of blood from volunteer donors on the spot. PRINCIPLE OF THE ASSAY Rapid HCV Ab test employs chromatographic lateral flow device in a cassette format. Colloidal gold conjugated goat anti-human IgM and mouse anti-human IgG are dried and immobilized on the fiberglass strip. HCV antigens are immobilized at the Test Zone (T) and goat anti mouse IgG antibodies are immobilized at the Control Zone (C). When the sample is added, it migrates by capillary diffusion rehydrating the gold conjugate. If present in sample, HCV antib