English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Background The Listeria genus comprises ten different species, however, only two of them L. monocytogenes and L. ivanovii are pathogenic. Although being a well-known pathogen, its detection methodologies are still limited. The goldstandard technique involves enrichment, isolation, and biochemical characterization, which can take about 7 days [1]. In addition, since both pathogenic and non-pathogenic species are present in contaminated food, it is important to detect them both [2]. This way, new methods, such as the immunodetection using monoclonal antibodies (MAbs), have been developed to reduce the detection time of Listeria spp.. Recently, our group described a hybridoma clone secreting a MAb of the IgM isotype, called MAb3F8, that reacts exclusively with an antigen of 30 kDa (P30) present in all Listeria spp. evaluated [3]. In the present work, we produced and initially characterized, by ELISA and Western blot, other two novel antibodies against P30 to be used in Listeria spp. immunodetection assays.

Partial characterization of two novel monoclonal antibodies for Listeria spp. Immunodetection