GraceTree COVID-19 IgM/IgG
Rapid differential detection kit for IgM and IgG against COVID-19 in human serum, plasma and whole blood
Feature & Type : IgM/IgG
1) COVID-19 IgM/IgG : blood test
2) Dual-band results for simple interpretation
3) Multivariable analysis of immunoglobin IgG & IgM
4) Positive percent agreement (PPA) = 96.0%
Negative percent agreement (NPA) = 98.99%
5) Room temperature storage ( 2~30C / 36~86F )
6) Time to result : 2 min
7) Expiration date of this kit is 6 months after its manufacture date
8) MATERIALS PROVIDED
- Test device individually foil-pouched with a desiccant
- Assay solution in dropping bottle
- Capillary tube for sample loading
- Instructions for Use
- Packing: 1 box of 25 Test units
- Product Origin : South Korea
- Certificate : FDA EUA Certificate will be proved near 15. September. 2020
- Shipping Terms : FOB
- Payment Terms : T/T
- MOQ : Under Discussion
- Contract : Direct contract seller / Depending on volume, direct contract with a subsidiary of seller which is listed on stock market(in S.Korea)
- LOI, POF needed for seller
KOSTEC can supply Korean rapid test kits, which are not only faster and easier in test but alsoprovide accurater test results. Also price is very much attractive! If you have any interest in this test kits, do not hesitate to contact me. Thanks!
Although the development cycle of antigen detection is relatively long, its
1. Sensitivity and specificity are higher than antibody detection
2. The pathogen can be detected at the initial stage of infection
3. Short TAT and simple operation.
4. No professional technicians and equipment are required, and the test can be completed in 15 min.
5. Home use.
6. Personal test.
Our Covid-19 rapid test kits are a serology test using a novel way to identify to identify exposure to the Covid-19 virus by the identification of the IgM/IgG antibodies through a sample of serum, plasma
or whole blood. The presence of the antibodies is revealed in 15 minutes and does not require any specialised laboratory equipment for the execution of the test.
Test kits are packaged with 25 sealed pouches holding the test cassettes, an instruction set, 25 capillary tubes for making 25 tests and a bottle of 3ml with buffer solution to execute 25 tests. The test pouch contains the test cassette and a sterilizer pad to be used to disinfect the fingertip in case of fingerprint blood sampling.
(A) Name of product: COVID-19 IgM/IgG Antibody Rapid Test
(B) Price $4 EXW
(c) Origin: Canada
(d) Features:
Artron COVID-19 IgM/IgG Antibody Test is a rapid, qualitative, and convenient immunochromatographic in vitro assay for the differential detection of IgM &/or IgG antibodies to SARS-COV-2 in human serum, plasma or whole blood samples. The device is designed to aid in the determination of recent or previous exposure to SARS-COV-2 virus tracking the bodyâ??s immunity status to the virus after SARS-COV-2 infection.
(E) HS code:382200
(F) 20,000 units
(g) Carton Size (LxWxH cm) 59*41*37 - 2,200 test per carton. 17.6kg.
25,000 kits per pallet.
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* NEW* Covid-19 ANTIGEN RAPID TEST KIT *NEW * with CE Mark EU APPROVED | Collodial Gold Method | 15 Minutes Rapid
Covid-19 Rapid Antigen Test Kit | Collodial Gold Method
Accurate: 96.1% sensitivity, 96.67% specificity compared with PCR
FAST: only 15 minutes required
EASY-TO-USE: no special requirements
Room temperature storage
MOQ 2000 units (25pcs) per unit
MAX 300.000 units PER DAY
Payment terms
100% TT in Advance
Lead time 7 days
Global delivery
Results
Usage/Application Hospital
Type Rapid Test Kit
Results 3 mins
Packaging Size 100 Tests
Country of Origin Made in India
The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.
SALIENT FEATURES
Rapid visual test ,based on Flow Through Technology.
Differential detection of HIV-1 & HIV-2.
Detection of group O & subtype C
Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2.
100% sensitivity & 100% specificity as per WHO Evaluation.
Shelf life 15 months at 2-8�°C
Available in convenient pack sizes-10 Tests, 50 Tests and 100 Tests.
Results within 3 minutes.
No instrument required.
In built quality control dot.
Our LH rapid test is based on the theory of enzyme interaction. It could be used to detect the content of LH atom in urine speciment. And the colour change will identify the result directly. Assisting with the result,doctor could judge whether the patient is pregnant .
Our product is based on the theory of enzyme interaction. It is used to detect the HCG atom in urine speciment. The colour change could identify the test result directly. Assisting with the result,doctor could judge whether the patient is pregnant or not.
Fapon Biotech provide gene engineering recombinant antigens and antibodys of HIV type 1¿¬¿«2 and group O, which can be used in ELISA and Rapid Test Kit, with high sensitive specific and stability.
Intended Use
Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture.
Contents of Kit
Flu A + B Test Card 20 ea
Sample Extraction Buffer 1 ea
Extraction Tube 20 ea
Nozzle With Filter 21 ea
Sterilized Swab 20 ea
Tube Stand 1 ea
Instructions For Use 1 ea
Storage And Stability
Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial.
Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after the expiration date.
3. The test device should remain in the sealed pouch until use.
4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test.
5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers.
6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation.
7. Visibly bloody samples should not be used for the testing.
for Rapid test
HCV Core+NS3+NS4+NS5 (IgG indirect)
HCV Core+NS3+NS4+NS5 (for coating, Sandwich)
HCV Core+NS3+NS4+NS5 (for conjugating, Sandwich)
Fapon Biotech provide gene engineering recombinant antigens of HCV, which can be used in ELISA, Rapid Test Kit and research, with high sensitive specific and stability.
Quicking canine coronavirus ag rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine coronavirus (ccv ag) in dog's feces or vomit.
