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
Hygisun rapid test is used for the qualitative detection of COVID19 in posterior oropharyngeal saliva, sputum and stool samples. Home use.
Stock in Germany.
We are A3 International, a company located in the 22 @ district of Barcelona and we are dedicated to the import and export of all kinds of products. Currently with the focus of providing material to combat COVID-19.
- Saliva and nasopharyngeal antigen test from
- Syringes from
- FFP2 masks
- Isolation and surgical gowns
- Protective suits
A pregnancy test can confirm if a woman is pregnant. The test can be carried out at home or in the doctor's office. A pregnancy test is around 99 percent reliable. It works by measuring levels of a hormone called human chorionic gonadotropin (HCG).
I-can is a test kit, which helps to detect pregnancy. Every woman is excited to know whether she has conceived or not. This I- can kit will help you to confirm pregnancy. I-can detects pregnancy in five minutes. It confirms pregnancy by detecting the presence of human chorionic gonadotropin hormone (pregnancy hormone) in the urine. It gives an accurate estimation of pregnancy. Major benefit of this kit is that it is very simple to use and you do not require any assistance to determine pregnancy by using this kit.
INTENDED USE
Easy-Sweet hCG Test Midstream is an in vitro diagnostic (IVD) qualitative test for rapid detection of hCG in urine. This test is designed for self-testing use only.
PRINCIPLE
Easy-Sweet. hCG Midstream is two-side sandwich immunoassay for the qualitative determination of human chorionic gonadotropin (hCG) in urine. The membrane was precoated with anti alpha hCG capture antibodies on the test band region and goat anti mouse on the control band region. During the test, the urine specimen is allowed to react with anti beta hCG monoclonal antibody-colloid gold conjugate, which was predried on the test Midstream. The mixture then moves forward on the membrane by the capillary action. For a positive specimen, the conjugate binds to the hCG forming an antibody-antigen complex. This complex is captured by anti alpha hCG antibody on the test region to produces a visual pink color band when hCG concentration in specimen is equal to or greater than 25 mIU/ml. Regardless of the presence of hCG, as the mixture continues to move across the membrane to the control band region, the complex is captured by immobilized goat anti mouse antibodies to form a distinct pink colored control band. The presence of the control band indicated: 1) a normal flow is obtained, 2) antibody pre-coated on control line and colloidal gold conjugate are functional.
General Information
One-Step Chlamydia Rapid Test (Swab/Urine) is detection of Chlamydia trachomatis in female cervical swab, male urethral swab and male urine specimens to aid in the diagnosis of Chlamydia infection.
Detection limit:1*103IFU/ml
Specimen: Swab/Urine
Reading Time : 10min
General Information
The Urinalysis Reagent Strips (Urine) are firm plastic strips onto which several separate reagent areas are affixed. The test is for the detection of one or more of the following analytes in urine: Ascorbic acid, Glucose, Bilirubin, Ketone (Acetoacetic acid), Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite , Leukocytes and so on.
The Herpes Simplex Virus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of IgG antibodies to Herpes Simplex Virus (HSV) in human serum/plasma samples.
HSV-1 is usually associated with infection in oropharyngeal area and eyes, while HSV-2 causes mostly genital and neonatal infections (5, 6), however, the tissue specificity is not absolute (7). HSV-2 can be isolated occasionally from the oropharynx and 5-10% of primary genital infections may be caused by HSV-1. Infants infected with HSV appear normal at birth, but almost invariably develop symptoms during the newborn period (5, 8, 9). Neonatal HSV infection may remain localized or become disseminated. Localized infection may involve one or a combination of sites. These are skin, eyes, mouth or the central nervous system. Disseminated infection is manifested by pneumonitis, hepatitis, disseminated intravascular coagulopathy and encephalitis. Of the infants with neonatal HSV, about one half of those surviving will develop severe neurological or ocular sequelae. A number of serological procedures have been developed to detect antibodies to HSV. These include complement fixation, indirect immunofluorescent antibody, plaque neutralization, and ELISA (6, 8, 10). Antibody of the IgG class is produced during the first 2-3 weeks of infection with HSV and exists only transiently in most patients. Serologic procedures, which measure the presence of IgG antibodies, help discriminate between primary and recurrent infections, since IgG antibodies is rarely found in recurrent infections. High affinity IgG antibodies to HSV, if present in a sample, may interfere with the detection of IgG specific antibody (9). High affinity IgG antibody may preferentially bind to HSV-1 antigen leading to false negative IgG results. Also, rheumatoid factor, if present, along with antigen specific IgG, may bind to IgG causing false positive IgG results. Both problems can be eliminated by deactivating IgG in the sample before testing for IgG.
General Information
One-Step Tetracycline Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Tetracycline residue in Milk,Honey,Tissue extract and Aquatic products.
Detection limit: Milk 100 ppb ,Honey 20ppb , Tissue extract 100 ppb , Aquatic products 100ppb
Specimen: Defatted milk, Honey, Tissue extract, Aquatic products
Reading Time : 5-10min
General Information
One-Step Beta-Lactam Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Beta-Lactam residue in milk.
Specimen: Milk
Reading Time : 5-10min
General Information
One-Step Nitrofurans Rapid Test are competitive immunoassay for the semi-quantitative detection of the presence of AOZ,AMOZ, AHD, SEM residue in animal tissue.
Detection limit:AOZ 1ppb , AMOZ 1ppb , AHD 1ppb , SEM 1ppb
Specimen: Animal tissue
Reading Time :10-15 min
One Step Troponin Test (Whole blood/Serum/Plasma
FOR IN VITRO DIAGNOSTIC USE ONLY
SPECIMEN COLLECTION
1. Testing should be performed immediately after the specimens have been collected. Do not leave the specimens at room temperature for prolonged periods. Specimens may be stored at 2-8C for up to 3 days. For long-term storage, specimens should be kept below -20C.
2. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
MATERIALS PROVIDED
1. Test cards individually foil pouched with a desiccant
2. Plastic dropper
3. Package insert
MATERIALS REQUIRED BUT NOT PROVIDED
1. Timer/clock
2. Pipette
3. Controls
ASSAY PROCEDURE
1. Read package insert carefully before testing. Allow the test devices, whole blood, serum or plasma to equilibrate to room temperature (15-30C) prior to testing. Do not open pouches until ready to perform the assay.
2. Remove the test device from the foil pouch and use it as soon as possible.
3. Place the test device on a clean and level surface. Hold the dropper provided vertically and transfer 3 drops of specimen (100�µl) to the specimen well (S) in the test device.
4. Wait for the red line(s) to appear. The result should be read between 10 to 15 minutes.
INTERPRETATION OF RESULTS
1. Positive Two colored lines should be observed in the viewing window. The line in the test region (T) is the probe line; the line in the control region (C) is the control line, which is used to indicate proper performance of the device. The color intensity of the test line may be weaker or stronger than that of the control line.
2. Negative The control line appears in the test window, but the test line is not visible.
3. Invalid No line appears in the control region. Under no circumstances should a positive sample be identified until the control line forms in the viewing area. If the control line does not form, the test result is inconclusive and the assay should be repeated.
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