Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/11753
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dc.contributor.authorSonavane, Avinashen_US
dc.date.accessioned2023-06-08T11:34:41Z-
dc.date.available2023-06-08T11:34:41Z-
dc.date.issued2023-
dc.identifier.citationBehera, A., Biswas, M., Ergün, S., Karnati, S., & Sonawane, A. (2023). Detection of peroxisomal proteins during mycobacterial infection doi:10.1007/978-1-0716-3048-8_9 Retrieved from www.scopus.comen_US
dc.identifier.issn1064-3745-
dc.identifier.otherEID(2-s2.0-85151043444)-
dc.identifier.urihttps://doi.org/10.1007/978-1-0716-3048-8_9-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/11753-
dc.description.abstractPeroxisomes are ubiquitous organelles with essential roles in lipid and reactive oxygen species (ROS) metabolism. They are involved in modulating the immune responses during microbial infection, thus having major impact on several bacterial and viral infectious diseases including tuberculosis. Intracellular pathogens such as Mycobacterium tuberculosis (M. tb) employ various strategies to suppress the host oxidative stress mechanisms to avoid killing by the host. Peroxisome-mediated ROS balance is crucial for innate immune responses to M. tb. Therefore, peroxisomes represent promising targets for host-directed therapeutics to tuberculosis. Here, we present protocols used in our laboratory for the culture of M. tb and detection of peroxisomal proteins in M. tb infected macrophages. © 2023, The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.en_US
dc.language.isoenen_US
dc.publisherHumana Press Inc.en_US
dc.sourceMethods in Molecular Biologyen_US
dc.subjectImmunofluorescenceen_US
dc.subjectMycobacterium tuberculosisen_US
dc.subjectPeroxisomesen_US
dc.titleDetection of Peroxisomal Proteins During Mycobacterial Infectionen_US
dc.typeBook Chapteren_US
Appears in Collections:Department of Biosciences and Biomedical Engineering

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