THE ONE STEP ANTI-DENGUE (IGM & IGG) TRI-LINE TEST IS A COLLOIDAL GOLD ENHANCED, RAPID IMMUNOCHROMATOGRAPHIC ASSAY FOR THE QUALITATIVE DETECTION OF ANTIBODIES (IGM & IGG) TO DENGUE VIRUS (DV) IN HUMAN WHOLE BLOOD, SERUM OR PLASMA. THIS TEST IS A SCREENING TEST, AND ALL POSITIVES MUST BE CONFIRMED USING AN ALTERNATE TEST SUCH AS WESTERN BLOT. THE TEST IS INTENDED FOR HEALTHCARE PROFESSIONAL USE ONLY.
The MOR Gold Rapid Screen Test Strip is a fast and easy to read membrane chromatographic immunoassay with no need for instrument. The method employs a unique combination of monoclonal and polyclonal antibodies to specifically identify Morphine in urine with a high degree of sensitivity.
Morphine, one of opiates�¢?? derivatives, is central nervous system stimulants that produce alertness, wakefulness, increased energy, reduced hunger, and an overall feeling of well-being. Morphine has been the preferred drug for the management of pain in cases of advanced cancer and other severe conditions. Morphine and other Opiates�¢?? metabolites may be detected in urine as a result of heroin morphine, codeine, or poppy seed intake. Administration of large doses of Morphine can cause tolerance and physiological dependence in users, and can lead to substance abuse. D-Morphine is controlled substances. GC/MS or immunoassay method has been developed for the determination of 300ng/ml for Morphine.
MOR Test PRINCIPLE
During a test labeled antibody-dye conjugate mixes with urine specimen and binds to the free drug if it is presented in the sample, to form an antibody-antigen complex. This complex prevents the formation of pink color bands in the test zone of the dip-stick if drug to be detected in specimen is above the detection levels (300ng/ml for Morphine). In case of absent of drug and its metabolites, unbound dye conjugate will bind to the antigens immobilized in the test zone to form a pink reaction line. To serve as a quality control for the assay, another pink line will always appears in the test zone regardless positive or negative result.
General Information
Items : MOR/MET/THC/AMP/MDMA/MTD/COC/TCA/BAR/BZO, up to 15 kinds of Drug Tests
Format: Strip, Cassette, Cup,and Panel
Specimen: Urine
Packaging Details:
Pouch+Box+Carton packaging
Beta lactam + Tetracycline Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Beta lactam and Tetracycline residue in milk.
KIT COMPONENT
1.6 plastic canister each containing 8 microwells and 8 strips
One-Step HBsAg Rapid Test is to detect the Hepatitis B Virus Surface Antigen in serum, plasma or whole blood.
Analytical sensitivity : 1ng/ml of HBsAg
Sensitivity :100% , Specificity : 100%
Specimen : Serum , Plasma or Whole Blood
Reading Time : 10 min
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The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.
PRECAUTION
1.For in vitro diagnostic uses only.
2.All patient samples should be treated as if capable of transmitting diseases.
3.Do not use test kit beyond expiration date.
4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
SUMMARY AND EXPLANATION OF THE TEST
It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.
PRINCIPLE
HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
INTENDED USE
Canine Distemper Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative
detection of canine Distemper virus (CDV Ag) in dog's secretions or serum.
Assay Time: 5-10 min
Sample: secretions or serum
PRINCIPLE
Canine Distemper Virus Ag 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 Distemper 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 Canine Distemper antigen in the sample.
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
EUA and CE pass
shelf life: 24months since manufacturing date
packing:2pcs/box,4pcs/box and so on
It is for self testing and OTC, for home use, school , and any group .
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
Monkeypoxvirus (MPXV) is a double-stranded DNA virus, a member of the orthopoxvirus genus within the Poxviridae family. MPXV falls into the same genus category as Cowpox (CPX), Variola (VARV), and Vaccinia (VACV) viruses. Poxviruses cause disease in humans and many other animals; infection typically results in the formation of lesions, skin nodules or disseminated rash. MPXV causes the disease in both animals and humans. It can be transmitted through animal-to human-contact e.g., animal bites, contact with animal bodily fluids etc., human-to-human contact e.g., touching infected lesions, inhalation of respiratory droplets, and eating infected meat that has not been thoroughly cooked. The incubation period for MPXV is typically 7â??14 days, but can range from 5â??21 days. Early onset symptoms of the disease are: swollen lymph nodes, aches and pains, fever and chills, headaches, and extreme fatigue. After 1-3 days, patients develop rashes, which progress to lesions, eventually scabbing over and falling off. The disease usually lasts for around 2-4 weeks. Swollen lymph nodes are typical of monkeypox. However, lesions may be haemorrhagic or coalesce into large bullae. The Monkeypox virus Antigen Rapid Test kit is a rapid test that utilizes a combination of Monkeypox antibody coated colored particles for the detection of Monkeypox antigen in human sample.
2019-nCoV Antigen Rapid Test Kit (Colloidal gold Assay)
Specimen Type: Siliva
Time to result: 15 minutes quick test
Storage: 18 months (room temperature)
Package: 25 Tests/Box ( 25 test cassettes + 25 Antigen extraction tubes + 25 Saliva sampling cups+ 25 Sampling droppers + 1 bottle Antigen extract R1 buffer+ 1 Test tube stand + 1 manual)
Relative Sensitivity: 90.3%.
New products will be launced in next 2 weeks, please mantain your attention!
2019-nCoV Antigen Rapid Test Kit (Colloidal gold Assay)
Specimen Type: Nasopharyngeal Swab
Time to result: 15 minutes quick test
Storage: 18 months (room temperature)
Package: 25 Tests/Box (25 pcs Nasopharyngeal swab + 25 test cassettes + 1 bottle Antigen extraction tube + 1 bottle Antigen extract R1)
Relative Sensitivity: >85%
Short test time: Within 15 Minutes
Accuracy: More than 90%
Easy operation: Throat/Nose swab, Saliva sample.
One-step solution - Lower cost with high efficiency
Components:
A 25 test cassettes
B 25 Antigen extraction tubes
C 1 bottle antigen extract R1
D 1 Test tube stand
E 25pcs Saliva Sample cups
F 25pcs disposable droppers
G 1 manual
Application:
A Suspected case test in epidemic area
B Early test of fever clinic and CDC
C Screening of primary medical institutions
D Inspection of floating population in public areas
Product Information:
Product Name : 2019-nCoV Antigen Rapid Test Kit
Methodology : Colloidal Gold Assay
Size: 25 Tests/box
Storage and Validity: Stored at 2-30 within 18 months
Specimen: Nasopharyngeal Saliva
Read the results in 15 minutes. A strong positive results may show within 15 minute.
But the negative result must be reported after 15 minutes. And the results after 20 minutes are not valid anymore.
Self-test received notified body approved CE Marking on April 1, 2021
A home test for the rapid qualitative detection of SARS-Cov-2 virus antigen in
anterior nasal swabs from individuals with or without symptoms or other
epidemiological reasons to suspect COVID-19
Performance Characterisitics
Sample tyep: nasal swab Time to result: 15-20 minutes
Sensitivity: 97.70% Specificity: 99.84% Accuracy:98.97%
Layperson study statistics
99.84% of non-professionals carried out the test without requiring assistance
99.82% of different types of results were interpreted correctly.
Specifications
1 Test/kit
Catalog No.: 1N40C5-2
Kit components:
1 Rapid SARS-CoV-2
Antigen Test Card (sealed foil pouch)
1 sterilized swab
1 extraction tube
1 sample extraction buffer
IFU
Tube holder on back of box
The lab indicated that the recombinant protein of Indian mutant (B.1.617.2),
A.23.1(Unit Kingdom), AT.1 (Russia), B.1.1.7(Unit Kingdom), B.1.351 (South Africa),
B.1.616 (France), B.1.621 (Colombia), C.36 (Egypt), C.37 (Peru), P.1 (Japan/Brazil),
P.2 (Brazil) can be detected by Jinwofu SARS-CoV-2 Antigen Test Kit.
For the newly descovered mutant Omicron(B.1.1.529), we performed sequence
alignment analysis on its mutation sites, and found that all the mutation sites were
outside the epitope region recognized by the monoclonal antibody selected by our company.
By bioinformatics analysis, Jinwofu SARS-CoV-2 Antigen Test Kit can also effectively detect
mutant Omicron(B.1.1529)
