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Feline Leukemia Virus Ag Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Leukemia Virus antigen (FeLV Ag) in cat's blood.
Assay Time: 10 -15 min
Sample: serum, plasma or blood

Feline Leukemia Virus Ag Rapid 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 FeLV 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 FeLV antigen in the sample.

It can be used for rapid screening of carriers of the virus that are symptomatic or asymptomatic. Recent studies suggest that a high percentage of patients show no clinical symptoms of the virus, thus screening patients is vitally important. The test is ideally suited for hospitals, clinics and test laboratories.

VETlabs Feline Panleukopenia Viraus (FPV) Ag Test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for rapid and qualitative detection of Feline Panleukopenia Virus in cat's feces or vomit.

VETLabs Toxoplasma IgM/IgG test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for the rapid and qualitative detection of Toxoplasma IgM/IgG in cat's blood. The test device has a testing window, coated by an invisible T (test) zone and C (control) zone. When a sample is applied to the sample well on the device, the reagent will laterally flow on the surface of the test strip. If there is enough Toxoplasma IgM/IgG in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid test. By the means, the device can accurately indicate the presence of Toxoplasma IgM/IgG in the specimen.

Kit components: 5 test per box and/or 10 test kit per box in an individual foil pouch with a desiccant and disposable dropper, EDTA blood collection tube, Assay buffer bottle, Instruction manual

VETlabs Canine Parvovirus (CPV) Ag/Canine Coronavirus (CCV) Ag Combo test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for the rapid and qualitative detection of Caine Parvovirus and Canine Coronavirus in dog's feces. The test device has a testing window, coated by an invisible T (test) zone and C (control) zone. When sample is applied into the sample well on the device, the reagent will laterally flow on the surface of the test strip. If there is enough CPV Ag/CCV Ag 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 CPV Ag/CCV Ag in the specimen.

"FactView Malaria Rapid PF/PV" likely refers to a diagnostic test for the rapid detection of Plasmodium falciparum (PF) and Plasmodium vivax (PV), two species of malaria parasites. Here's more information about this type of diagnostic test:

Purpose: The FactView Malaria Rapid PF/PV test is used for the rapid detection of malaria infection caused by the Plasmodium falciparum and Plasmodium vivax parasites. Malaria is a serious infectious disease transmitted by the bite of infected Anopheles mosquitoes.
Principle: The test is based on immunochromatographic principles, where specific antibodies are used to detect the presence of malaria antigens in a patient's blood sample. The presence of the PfHRP2 antigen indicates P. falciparum infection, while the presence of the pLDH antigen indicates P. vivax infection.
Components: The FactView Malaria Rapid PF/PV test typically includes test cassettes, sample droppers, buffer solutions, and desiccants. The test cassettes contain pre-coated membranes with specific antibodies for detecting malaria antigens.
Procedure: The test procedure involves collecting a small amount of blood from the patient (usually obtained via finger prick) and applying it to the sample well of the test cassette. Buffer solution is then added, allowing the blood sample to migrate along the test strip. Results are typically visible within 15-20 minutes.
Interpretation: The appearance of colored lines on the test strip indicates the presence or absence of malaria antigens. A visible line in the control region indicates that the test is valid. Additional lines in the test regions indicate positive results for P. falciparum and/or P. vivax antigens.
Sensitivity and Specificity: The FactView Malaria Rapid PF/PV test demonstrates high sensitivity and specificity for detecting malaria infections caused by P. falciparum and P. vivax parasites. However, like all diagnostic tests, false-positive and false-negative results are possible and should be interpreted in conjunction with clinical findings.
Utility: Rapid diagnostic tests like the FactView Malaria Rapid PF/PV provide a quick and convenient method for diagnosing malaria infections in resource-limited settings, where access to laboratory facilities and microscopy may be limited.
Limitations: While rapid diagnostic tests are valuable tools for malaria diagnosis, they have limitations compared to more sensitive methods such as microscopy or molecular testing. Factors such as test storage conditions, operator technique, and the stage of infection can influence test performance.

Products we have access to for the US Market

OTC:
iHealth 2 pack - 4-7 business days from payment

AccessBio 2 pack - Available within 3-5 business days

FlowFlex 1 Pack- Available for delivery after the 7th Feb

Roch 5 Pack- 5 day lead time from payment

SD-Biosensor 1 or 2 pack: 100,000 available daily CIF/DDP from South Korea

On/Go: Weekly allocation is available on-going, Made in USA!

POC:

Sienna
Celltrion
Indicaid
GenBody
Spring Health

OTG: ICPO x Invoice x Inspect and Pay products are available for spot purchases, at a premium price.
OTG or OTW: Wire and Ship products are sold with CHAIN OF CUSTODY, AWB, BOL or other proof of Allocation... at slightly better rates.
Production opportunities, on-going Allocation, or larger volumes are sold at the best price, with tiered pricing for longer duration contracts.

There are financing opportunities available:
Factoring ICPO x CounterSigned Invoice for Gov POs, Hospital Organizations, and Fortune 500 Companies.
Everyone else must Fund Escrow, or Block Funds, with explicit verbiage guaranteeing the release once the order reaches America, clears customs, and is available for physical inspection/ delivery to the clients destination.

Description
Foot-and-mouth disease virus (FMDV) causes an acute vesicular disease of cloven-hoofed animals and continues to be a threat to livestock worldwide with outbreaks causing severe economic losses.
RIDX FMDV 3Diff/PAN Ag Combo Test Kit is a lateral flow chromatographic immunoassay for the qualitative detections of all 7 serotypes antigens of FMDV in bovine or porcine samples.
3Diff Ag Test: FMDV 3Diff detects FMDV Asia1, type A, and type O antigens. Three test lines (AS, A, O) and the control (C) line on the surface of the device.
PAN Ag Test: FMDV PAN detects all 7 serotypes (type O, type A, type C, Asia1, SAT1, SAT2, and SAT3) of FMDV antigens. The test line (PAN) and the control (C) line on the surface of the device.
If the FMDV antigens exist in the sample, that bind to the gold-conjugated FMDV antibodies. The complexes move through the membrane by capillary force and respond to the FMDV antibodies on the test line, resulting in a red line. The control line indicates that the test is performed correctly.
The highly selective and sensitive four monoclonal antibodies to FMDV are used as capture and detector in RIDX�® FMDV 3Diff/PAN Ag Combo Test Kit. These antibodies are capable of detecting FMDV antigens in bovine and porcine samples with high accuracy.

Specimen
Bovine or porcine saliva, tissue or vesicular fluid around lip, tongue, gums, nose, or hoof

Components
FMDV 3Diff/PAN Ag combo test device (10 tests)
Disposable swab (10 ea)
Sample dilution buffer (1 vial)
Disposable dropper (10 ea)
Sample tube (10 ea)

Features
Clinical Sensitivity
1. Type O 88.2% (n=60/68) vs. PCR
2. Type A 100% (n=70), Asia1 100% (n=62), SAT1 100% (n=20), SAT2 100% (n=20), SAT3 100% (n=20), C 100% (n=20), in spiking samples with virus (titer: 1.0x105 TCID50/ml or higher)
Clinical Specificity
1. Type O, type A and PAN: Bovine 100% (n=92), Swine 100% (n=400)
2. Type Asia1: Bovine 100% (n=92), Swine 99.5% (n=398/400) Differential diagnosis of 3 different serotypes (O, A, Asia1) of FMDV
Concurrent diagnosis both of viral common antigens (all 7 serotypes) and serotype-specific antigens (O, A, Asia1)

Packages
10 Tests/Kit
12 Kits/Box (120 Tests/Box) or 40 Kits/Box (400 Tests/Box)

The cardiac troponin i fast test kit (colloidal gold) is intended for use together with the fia8000 quantitative immunoassay analyzer (fia8000). The product employs colloidal gold immunochromatogrphy to determine ctni in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify ctni specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of ctni.

Then insert test card into the fia8000 quantitative immunoassay analyzer, the concentration of ctni is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for NT-proBNP (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NT-proBNP in human serum, plasma, or whole blood specimens. One monoclonal antibody and one polyclonal antibody are employed to identify NT-proBNP specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NT-proBNP.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NT-proBNP is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for PCT (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine PCT in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify PCT specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of PCT.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of PCT is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for B2-MG (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine B2-MG in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify B2-MG specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of B2-MG.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of B2-MG is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for mAlb (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine mAlb in human urine specimen. Polyclonal antibody and recombinant antigen are employed to identify mAlb specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of mAlb.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of mAlb is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

The One Step Test for NAGL (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NGAL in human urine specimen. Monoclonal antibody and polyclonal antibody are employed to identify NGAL specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NGAL.

Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NGAL is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.

In the past two months, China was infected by the COVID-19( Noval Coronavirus), in order to diagnose the diseases earlier, Encode team work hard and finally develop the COVID-19 IgM/IgG rapid test kit, which clinical positive detection rate is over 90%.