General information One-step influenza a/b test is detection influenza type a and type b nucleoprotein antigen extracted from the nasal swab specimen. Sensitivity : 91.3% , specificity : 95.7% Detection limit:5.1x105tcid50/ml Specimen: nasal swab Reading time : 15-20min
Uncut Sheet Toxoplasma Gondii IgG/IgM Tri-Lines Rapid Test Specimen :Whold Blood/Serum/Plasma INTENDED USE The One Step TOXO IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii in Whole Blood /Serum / Plasma to aid in the diagnosis of TOXO infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of serologic tests for antibodies to Toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as The Toxo IgM/IgG Rapid Test (Whole Blood/Serum/Plasma) was introduced into the clinic for the serodiagnosis of Toxoplasma gondii infection. One step TOXO IgG/IgM Test is a simple, visual qualitative test that detects TOXO antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
Syphilis Test INTRODUCTION Anti-Syphilis Test is a rapid direct binding test for the visual detection of anti-syphilis antibodies in serum as an aid in the diagnosis of syphilis infection. Test results are read visually without any instrument. It is based on the principle of double antigen sandwich immunoassay for determination of syphilis antibodies in serum. Purified recombinant syphilis antigens are employed to identify anti-Syphilis antibodies specifically. This one step test is very sensitive and only takes about 10 to 20 minutes. Syphilis Test SPECIMEN COLLECTION For serum, collect blood into a container without anticoagulant. Allow the blood to clot and separate the serum from the clot. Use the serum for testing. If the specimen cannot be tested on the day of collection, store the serum specimen in a refrigerator or freezer. Bring the specimens to room temperature before testing. Do not freeze and thaw the specimen repeatedly. Syphilis Test PROCEDURE Strip 1.When you are ready to begin testing, open the sealed pouch by tearing along the notch. Remove the test from the pouch. 2. Immerse the strip into the container with the arrow end pointing towards the container. Do not immerse past the MAX (maximum) line. Take the strip out after 8-10 seconds and lay the strip flat on a clean, dry, onabsorbent surface (e.g., mouth of the serum container). 3.Wait 10-15 minutes and read result. Do not read results after 20 minutes. Cassette 1. Open a pouch containing a cassette, lay the cassette. 2. Using the plastic pipettor provided, draw about 2-3 drops (100mL) the sample into the sample well of the cassette. 3. Read results within 10-15 minutes. Do not read results after 20 minutes. INTERPRETATION OF RESULTS Negative: Only one pink band appears on test region of the Cassette. This indicates that there is no detectable Anti-Syphilis in the serum. Positive: Two pink bands appear on test region of the Cassette. This indicates that the specimen contains detectable amount of Anti-Syphilis. Invalid: If without colored band appears on test region, this is an indication of a possible error in performing the test. The test should be repeated using a new device. Syphilis Test PRECAUTION: 1.�Must use fresh specimen and avoid repetitive freezing, the result will be invalid 2.�Use it before expiry date. 3.The package of kit should not be opened until it reaches the room temperature if it taken out from the refrigerator. 4�.Old Serum can not be used. If the serum is thick, it can be used only after being separated. Syphilis Test LIMITATIONS The test is for in-vitro diagnostic use only.
INTENDED USE The HCG s/u Gold Rapid Screen Test(RST)is a chromatographic immunoassay for the early detection of human chronic gonadotropin (HCG) in serum/plasma or urine specimens. INTRODUCTION HCG is a glycoprotein hormone secreted by the developing placenta during pregnancy. The concentration of HCG in serum is approximately equal to the concentration in urine. The concentrations of HCG in urine and serum continue to rise during the first trimester of pregnancy to as high as 100,000 mIU/ml. HCG appears in urine shortly after conception, and continues to increase during the early stages of pregnancy, making it an excellent indicator for the detection of pregnancy. PRINCIPLE The membrane of the test device was coated with anti HCG antibodies on the test region and goat anti mouse IgG antibodies on the control region. During the test, urine specimen is allowed to react with the HCG monoclonal antibody-colloid gold conjugate, which was pre-dried on the test strip. The mixture then moves upward on the membrane chromatographically by capillary action. For a positive specimen, the conjugate binds to the HCG forming an antibody-antigen complex. This complex is captured by anti HCG antibody immobilized on the test region (T) and produces a pink color band when HCG concentration is equal to or greater than 25mIU/ml. Absence of this colored band in the test region suggests a negative result. To serve as a procedural control, a colored band at the control region(C) will always appear regardless the presence or absence of HCG. STORAGE
INTENDED USE Giardia Ag Feces Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Giardia antigen in feces. Assay Time: 5-10 min Sample: Feces PRINCIPLE Giardia Ag Feces Rapid 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 Giardia 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 Giardia antigen in the sample..
Specification Strength/ Size Packing Size Packed In Malaria Antigen PF/ PV Card Test 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In Malaria Antigen PF/ PV Card Test 50 Tests 50 Box Pack Malaria Antibody PF/ PV Card Test 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In Syphilis Test Card 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In Typhoid IgG/IgM 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In HCG Mini Card 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In HCG Mini Card 50 Tests 50 Box Pack HCG Big Card 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In HCG Test Strip (Dipstick) 50 Tests 50 Box Pack
Specification Strength/ Size Packing Size Packed In Reagent Strip for detection of Albumin & Glucose in Urine 100 Tests 100 Box Pack
Specification Strength/ Size Packing Size Packed In HCV Test Cards 10 Card Test Per Pack 50 Box Pack
Specification Strength/ Size Packing Size Packed In Dengue Test 50 Card Test Per Pack 10 Box Pack
Specification Strength/ Size Packing Size Packed In Glucose Test Bottle of 100T
Specification Strength/ Size Packing Size Packed In Protein Test Bottle of 100T
Specification Strength/ Size Packing Size Packed In Glucose, Bilirubin, Ketone, Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite and Leukocytes Bottle of 100T
Molecular Diagnostic Tests for SARS-CoV-2 Other Tests for SARS-CoV-2 Serology and Other Adaptive Immune Response Tests for SARS-CoV-2 IVDs for Management of COVID-19 Patients
The CERA-PET Multi Test meter (M 400V) is intended for use in veterinary and medical professional setting to monitor blood glucose, lactate level in dogs and cats. It is also intended for use in the home setting to monitor blood glucose, lactate levels in dogs and cats. The CERA-PET Multi Test Meter is intended for in vitro diagnostic use.
