Test Kits #2809361

Recombigen Dengue Ab test is a rapid card test based upon lateral flow immuno assay for the qualitative detection of IgM and IgG antibodies to Dengue virus in human serum / plasma. The nitrocellulose membrane is immobilized with anti human IgG, anti human IgM and control line protein. The colloidal gold conjugate contains recombinant protein of Dengue. Recombigen Dengue Ab test is available in multiple of 10T pack. Each pack contains individually pouched test devices, sample droppers, buffer vial and product insert. It has shelf life of 24 months from date of manufacturing if stored at 2-30 C under sealed conditions.

Recombigen ClearTyphi Typhoid test is intended used for qualitative detection of IgM and IgG antibodies to S.typhi in human serum / plasma / whole blood as in aid of diagnosis of typhoid. It is based upon lateral flow immuno assay and LPS antigen to S.typhi have been used for coating on nitro cellulose membrane and anti human IgM / Protein-A is conjugated to colloidal gold to have better sensitivity and specificity. Specimen of choice is serum / plasma / whole blood and result can be obtained within 5-20 minutes. Recombigen ClearTyphi Typhoid test is available in 40T pack and has shelf life of 24 months from date of manufacturing if stored at 2-30 C under sealed conditions.

Clear&Sure HCG / Pregnancy card test is intended used for qualitative detection of HCG (Human chorionic gonadotropin) in human urine as in aid of early diagnosis pregnancy. It is based upon lateral flow immuno assay and highly specific monoclonal /polyclonal antibodies to HCG have been used for coating on nitro cellulose membrane and colloidal gold conjugate in the test formulation to have better sensitivity and specificity. Specimen of choice freshly collected urine and result can be obtained within 5-10 minutes. Clear & Sure HCG card test is available in 50T pack and each kit contains individually pouched test cards, disposable droppers and product insert. It has shelf life of 24 months from date of manufacturing if stored at 4-30 C under sealed conditions. The Clear & Sure HCG test has excellent sensitivity and specificity with minimal detection limit of 25 mIU HCG/ml of urine.

The ASO latex test kit serology kit is intended for the qualitative and semi-quantitative measurement of antibodies to streptococcal exoenzymes in human serum. INTRODUCTIONThe group A -hemolytic streptococci produces various toxins that can act as antigens. One of these exotoxins Streptolysin O was discovered by Todd in 1932. 1A person infected with group A -hemolytic streptococci produces specific antibodies against these exotoxins, one of which is antistreptolysin O (ASO). The quantity of this antibody in a patient's serum will establish the degree of infection due to the -hemolytic streptococcal. 2The usual procedure for the determination of the antistreptolysin titer is based on the inhibitory effect that the patient's serum produces on the hemolytic power of a pretitrated and reduced Streptolysin O. 2-6 However, the antigen-antibody reaction occurs independently of the hemolytic activity of Streptolysin O. 7 this property enables the establishment of a qualitative and quantitative test for the determination of the ASO by agglutination of latex particles on slide. 2 PRINCIPLEASO test method is based on an immunological reaction between streptococcal exoenzymes bound to biologically inert latex particles and streptococcal antibodies in the test sample. The reagent has been adjusted in the way that presence of an ASO titer of 200 IU/mL or higher in the serum gives a visible agglutination of the latex particles without previous sample dilution

Pack Size-

1. 25 Test

2. 50 Test

3. 100 Test

Malaria is a serious parasitic disease characterized by fever, chills and anaemia and is caused by a parasite that is transmitted from one human to another by the bite of infected Anopheles mosquitoes. There are four kinds of malaria that can infect humans: Plasmodium falciparum, P. vivax, P. Ovale, and P. Malariae. In humans, the parasites (called sporozoites) migrate to the liver where they mature and release another form, the merozoites. The disease now occurs in more than 90 countries worldwide, and it is estimated that there are over 500 million clinical cases and 2.7 million malaria-caused deaths per year. At present, malaria is diagnosed by looking for the parasites in a drop of blood. Blood will be put into a microscope slide and stained so that the parasites will be visible under a microscope.

The Malaria Antigen Test contains a membrane strip, which is pre-coated with one monoclonal antobodies as one line across a test strip. One monoclonal antibody (test line 1) is specific to the P. falciparum histidine rich protein-2 (Pf HRP-2) and another monoclonal antibody test line 2) is P.vivax specific to the lactate dehydrogenase of plasmodium vivax species. Conjugate pad is dispensed with monoclonal antibodies conjugated to the colloidal gold, which specific to P.falcipuram histidine rich protein-2 (Pf HRP-2) and P.vivax specific to the lactate dehyogenase of plasmodium species. The Malaria Antigen Test is designed for the diagnosis of Plasmodium falciparum and Plasmodium vivax.

PRECAUTIONS

For professional in vitro diagnostic use only. Do not use after expiration date.

Do not eat, drink or smoke in the area where the specimens or kits are handled.

Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout testing and follow the standard procedures for proper disposal of specimens.

Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are being tested.

Humidity and temperature can adversely affect results.

STORAGE & STABILITY

The kit can be stored at room temperature or refrigerated (4-30C). The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.