Introduction to Immunochromatographic Strip

We have therefore developed an immunochromatographic strip (ICS) to enable rapid on-site detection of CyHV-2 by aquaculture facility staff.

We developed an antigen-ELISA (ag-ELISA) and a colloidal gold–based immunochromatographic strip for the rapid detection of avian A(H5) viruses.

LP-Ag was made into an immunochromatographic strip.

Based on the mAb produced, a fluorescent microsphere-based immunochromatographic strip assay (FM-ICS) and a gold nanoparticle-based immunochromatographic strip assay (GNP-ICS) were developed for the rapid and sensitive detection of CPM in herbal tea samples.

Based on the mAb, an immunochromatographic strip (ICS) was developed to qualitatively and quantitatively detect LCT in cabbage, parsley, spinach, and green tea samples.

Methodology/principal findings A cross-sectional study was undertaken to evaluate the diagnostic test performance of Isothermal Recombinase Polymerase Amplification (RPA) targeting Leishmania kinetoplast DNA, coupled with a lateral flow (LF) immunochromatographic strip, in a field setting and a laboratory reference center.

Based on this, a gold nanoparticles (AuNPs)-based immunochromatographic strip (ICS) test was established for the detection of VB6 in energy drinks and B-vitamin complex tablets.

The coloration results of the immune response are used as the basis for the determination of the detection target in combination with an immunochromatographic strip.

On the basis of this condition, an immunochromatographic strip (ICS) is proposed that could be applied in milk samples to test IM rapidly.

The purpose of this study was to develop an immunochromatographic strip test (ICT) based on a solid phase sandwich format immunoassay for the detection of T.

Samples were also subjected to different DATs: a gel minitube and an immunochromatographic strip kit used in clinics; neutral gel column cards, microtiter plates (at 4°, 22°, and 37°C), capillary tubes, and flow cytometry used in laboratories.

We noted the occurrence of false-positive results for COVID-19 in the colloidal gold-based immunochromatographic strip (ICS) assay in sera from patients with autoimmune diseases (ADs).

Antibodies against the selected peptide were conjugated to gold nanoparticles and incorporated into an immunochromatographic strip.

Develop the immunochromatographic strip assay for rapid on-site screening of azoxystrobin in vegetables.

This paper outlines the progress of detection methods for Bt Cry proteins from the past to recent advances, including not only relatively mature sensing systems such as enzyme-linked immunoabsorbent assay (ELISA) and immunochromatographic strip, but also some novel analysis approaches, for example, electrochemistry and fluorescence.

The immunochromatographic strip was prepared.

In this study, an advanced Bi semimetal/Zeolitic imidazolate frameworks hybrid material-based immunochromatographic strip (Bi/ZIF HM-ICS) sensor was developed for the sensitive detection of ACE.

In this study, we developed a monoclonal antibody (mAb)–based immunochromatographic strip for the detection of gamithromycin (GAM) residues in beef and milk samples.

We have developed a sensitive and rapid gold nanoparticle-based immunochromatographic strip (GNP-ICS) for the detection of phenacetin (PNCT) and paracetamol (PAP) using an anti-PNCT monoclonal antibody (mAb).

A colloidal gold-based immunochromatographic strip was developed with two McAbs to detect SARS-CoV-2 spike protein, which can play a potential role in monitoring vaccine quality.

This method has the advantages of high sensitivity and specificity due to the use of CRISPR/Cas12a technology, and it can be used for onsite testing with a portable testing instrument or immunochromatographic strips.

Nickel hydroxide nanoparticles [Ni(OH)2-NPs] synthesized by a complexation-precipitation method under hydrothermal conditions were employed as a probe in immunochromatographic strip tests for the selective detection of melamine.

We have developed a novel paper-based molecular pathogen diagnostic method by combining the direct loop-mediated isothermal amplification (Direct LAMP) in a paper reactor and an immunochromatographic strip (ICS) detection without any DNA preparation step.

Objective: To produce, purify, and characterize a polyclonal antibody against acrylamide (anti-AA) for an application to immunochromatographic strip tests for AA.

The cut-off values of the immunochromatographic strips for the four compounds in water were 5, 100, 100, and 100 μg/mL, respectively, indicating that the ic-ELISA and immunochromatographic strips we developed can be used to rapidly detect eugenol compounds in water.

1E7, to perform immunocolloidal gold strip treatment on cucumber samples, the PBS and the cucumber samples cutoff value of Immunochromatographic strips (ICS) was found to be 50 ng/ml; We conclude that ICS can rapidly detect pyrimethanil in cucumber samples.

To develop a rapid and easy detection method for Cronobacter species, especially in powdered infant formula (PIF), an immunoliposome-based immunochromatographic strip assay was developed using an anti-Cronobacter immunoglobulin G (IgG)-conjugated liposome and an anti-Cronobacter IgG-coated nitrocellulose membrane.

Urinary equol was measured using an immunochromatographic strip test.

In this study, a rapid and sensitive gold nanoparticle (AuNP) immunochromatographic strip is produced for detecting aflatoxin B1 (AFB1) in suspicious fungi-contaminated food samples.

005) by flow cytometry and immunochromatographic strip kit.

Immunochromatographic strips (ICS) were developed for the rapid detection of PZQ residues in mackerel.

A rapid, specific and sensitive method based on immunochromatographic strip test has been developed for the determination of 3.

AB blood typing was performed using an immunochromatographic strip.

In addition, the cut-off value of the immunochromatographic strip detection method in milk samples was 5 ng/mL.

A real-time, on-site rapid and sensitive detection method of low-molecular chemical pollutants was developed by an immunochromatographic strip based on the competitive reaction between the pesticide antigens and polyclonal antibody labeled with upconversion nanoparticles (UCNPs) bio-probes.

In this study, two monoclonal antibodies (MAbs) 16E6 and 11C1 against RSV and a colloidal gold-based immunochromatographic strip were developed for specific, sensitive, and rapid detection of RSV in rice plant and planthopper samples.

We evaluated an immunochromatographic strip for the detection of avian avulavirus 1 (Newcastle disease virus, NDV) based on a high-affinity monoclonal antibody (mAb) that specifically recognizes the hemagglutinin-neuraminidase (HN) protein.

BackgroundImmunochromatographic strips (ICSs) are a practical tool commonly used in point-of-care testing (POCT) applications.

ABSTRACT A rapid, specific and sensitive method based an immunochromatographic strip test has been developed for the determination of sodium nifurstyrenate (NFS) residues in fish.

An anti-rosiglitazone (RSG) monoclonal antibody (4G6) was prepared to develop an immunochromatographic strip for the detection of illicitly added RSG in hypoglycemic functional foods.

A rapid, specific and sensitive method based on an immunochromatographic strip test has been developed for the determination of IPRO residues in cucumber and apple.

Immunochromatographic strip (ICTS) nanosensors are one of the most popular point-of-care (POC) diagnostic devices currently available for rapid target screening.

Immunochromatographic strips (ICS) attract much attention as practical analytical tools, particularly for point of care testing.

ABSTRACT To monitor the levels of furaltadone in animal tissues, an immunochromatographic strip (immunostrip) based on quantum dot was developed for rapid detection of 3-amino-5-methylmorpholino-2-oxazolidinone (AMOZ), the metabolite of furaltadone.