Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : AR0151C
Use of conserved antigens allows pan-filaria tests to be applicable
Simple procedure provides alternative to diagnosis by blood smear
Use serum, plasma or whole blood
No restrictions on time of day for sample collection
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample diluent (1 bottle, 5 mL)
One package insert (instruction for use)
COVID-19 Rapid Test Kit IgG + IgM (Colloidal Gold) comes in packs of 40 tests and contains:
GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request.
To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away.
1. Nasopharyngeal
2. Nasal
3. Saliva
Price and Minumum Quantity
Price FOB in USD: negotiable 0.8 to 1.8Minimum Order Qty: None Pieces
Production Capacity: 3,000,000/monthPackaging: 20 Tests/kit, 30 Kits/box, 12 Boxes/pallet
Sample: Available. Sample Cost Born By Supplier
Product Model And Origin
Brand: GENEDIAModel: 643G-S (Saliva)
Seller Code: Genedia w covid 19 agHS Code: 3002.15
Standards: Ce
Competitive Advantages
Allow wider testing with fast test time (10 minutes)
All necessary materials provided / no equipment needed
Sensitivity: 93.33%, specificity: 100%
Free sample. no moq. price is negotiable. customized packing.
Other Details
20 tests / kit
24 months from the date of manufacture
2 ~ 30c(35.6 ~ 86f) available for room temperature deliver
In stock. fast delivery.
1 x Instructions for Use Manual
40 x Test Cassettes
1 x Buffer
40 x Dropper
CTK Biotech's ,
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
Number of Reactions(Preps)/Kit 30T
Brand CTK Biotech
Result Time (Rapid Kits) 20mins
Test Type Rapid Test
CAT No : R0234C
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
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We are the authorized first vendor of ADTech!
KFDA CE approved,
FDA Pending
Price : Negotiable
Pre-Clinical Test Report
Accuracy
- In total samples 93.3% (14/15) - In positive samples 91.7% (11/12)
1. Pre-Clinical Test summary
1) Pre-clinical test is fulfilled by Domestic large clinical laboratory with ADTech COVID-19 IgM/IgG RAPID KIT
2) Tests are made by total 15 samples with 12 positive and 3 negative samples
3) Clinical Laboratory tested the sample with Immunofluorescence Analysis
2. Pre-clinical test result
1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT
2) Test result by ADTechs RAPID KIT
- 4 negatives and 11 positives results in 15 samples
3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT
- 14 test results are same(including negative and positive results) - 1 samples test result are different(Positive Negative by ADTech
The Typhoid IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of anti-Salmonella typhi (S. typhi)G and IgM in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with S. typhi. Any reactive specimen with the Typhoid IgG/IgM 2.0 Rapid Test must be confirmed with alternative testing method(s).
The Cytomegalovirus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of Cytomegalovirus (CMV) in human serum/plasma samples.
Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients.
The Cytomegalovirus Rapid Test Device (Serum/Plasma) has been designed to detect CMV through visual interpretation of color development in the internal strip. The membrane was immobilized with antigens of CMV on the test region. During the test, the specimen is allowed to react with colored recombinant mouse anti-human IgM latex conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough CMV antibodies in specimens, a colored band will from at the test region of the membrane. Presence of this colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.
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.
Covd-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and dierential detection of IgG and IgM antibodies to 2019 Novel Corona Virus in human whole blood, serum or plasma.
Specification.jpg
Product: Rapid Diagnostic Test Kit
Item: Corona Virus Test Kit
Specimen: Whole Blood/Serum/Plasma
Format: Strip/Cassette
Port of Loading: Shanghai
OEM and ODM: OEM/ODM Welcome
Shipping: By UPS, FEDEX, DHL, TNT, by air or by sea
Note: Store this product in a cool and dry place, avoid direct sunlight, stay away from places that children can contact, and avoid eye contact. If you have allergies to this product, please stop using and consult a doctor.
COVID-19 Corona Virus Rapid Test Kit11.pngCOVID-19 Corona Virus Rapid Test Kit12.png
CTK BioTech's, CE certified, Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 �µL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
CAT No : R0063C. Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection Individually sealed foil pouches containing:
One cassette device
One desiccant
5 uL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
General Information
One-Step Chikungunya IgG/IgM Rapid Test is detection of IgG and IgM anti-chikungunya virus CHIK in human blood.
Sensitivity: 90.3% , Specificity: 100%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min
General Information
One-Step Leishmania IgG/IgM Rapid Test is detection antibodies IgG and IgM to the subspecies of the Leishmania donovani (L. donovani), the Visceral leishmaniasis causative protozoans in human blood.
Sensitivity: 91.2 % , Specificity: 99.5%
Specimen : Serum, Plasma or Whole Blood
Reading Time : 10 min
A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only.
INTENDED USE
The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection.
SUMMARY
Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4
The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen.
PRINCIPLE
The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
Supplier From
Incheon,
Incheon Gwang-yuk-si,
South Korea (Republic Of Korea)
We manufacture k cosmetics, deodorant & shampoo for pets, sanitary pads, mask obtained a patent, drug rapid test kit etc.
we are a contracted export agent . we export kimchi, korean sticky rice, inventory of various goods from major on line platforms. we provide extraordinary bulky price.
.Oem &odm , connect and find supplier or manufacturer
etc
Monkeypox IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)
is a solid phase immunochromatographic assay for the rapid, qualitative
and differential detection of IgG and IgM antibodies to monkeypox virus
in human whole blood, serum or plasma. This test provides only a
preliminary test result.
General Information
One-Step Dengue Rapid Test is to detect IgG&IgM antibodies in serum, plasma or whole blood.
For Dengue IgG/IgM Ab test:
Sensitivity : 99.9% , Specificity : 99.5%
Specimen : Serum , Plasma and Whole Blood
Reading Time : 10 min
Our COVID-19 rapid test kit can be used effectively on many levels for proper screening and strategic preparedness toward the pandemic. The test kit requires no sophisticated equipment nor laboratory settings. Our SARS-COV-2 Antibody Rapid Test Kit can be applied for screening of COVID-19 disease on the following:
General practitioners and external clinics level to detect previous SARS-COV-2 viral infections on both symptomatic and asymptomatic patients.
Determination of the immunity level of front-line healthcare workers, which can help in the development of pandemic preparedness strategies at national levels.
Epidemiological COVID-19 surveys at national and district levels for research purposes.
Airport screening for arriving /departing passengers to control the pandemic in the aviation industry.
Suspected cases exclusion to minimize cost and time spent in the RT-PCR testing procedures.
Screening on the national level to facilitate decision making regarding lockdown and curfew easing strategies.
Phoenix Bioscience is offering a competitive price for a high-quality kit that is made in Canada and used currently to combat the pandemic in most American cities.
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