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. 2015 Oct 1:(104):53053.
doi: 10.3791/53053.

Immunofluorescence to Monitor the Cellular Uptake of Human Lactoferrin and its Associated Antiviral Activity Against the Hepatitis C Virus

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Immunofluorescence to Monitor the Cellular Uptake of Human Lactoferrin and its Associated Antiviral Activity Against the Hepatitis C Virus

Andréa Allaire et al. J Vis Exp. .

Abstract

Immunofluorescence is a laboratory technique commonly used to study many aspects of biology. It is typically used to visualize the distribution and/or localization of a target molecule in cells and tissues. Immunofluorescence relies on the specificity of fluorescent-labelled antibodies against their corresponding antigens within a cell. Both direct and indirect immunofluorescence approaches can be used which rely on the use of antibodies linked with a fluorochrome. Direct immunofluorescence is less frequently used because it provides lower signal, involves higher cost and less flexibility. In contrast, indirect immunofluorescence is more commonly used because of its high sensitivity and provides an amplified signal since more than one secondary antibody can attach to each primary antibody. In this manuscript, both epifluorescence microscopy and confocal microscopy were used to monitor the internalization of human lactoferrin, an important component of the immune system, into hepatic cells. Moreover, we monitored the inhibitory potential of hLF on the intracellular replication of the Hepatitis C virus using immunofluorescence. Both the advantages and disadvantages associated with these approaches are discussed.

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References

    1. Odell ID, Cook D. Immunofluorescence techniques. J Invest Derm. 2013;133(1):e4. - PubMed
    1. Portugal J, Waring MJ. Assignment of DNA binding sites for 4’,6-diamidine-2-phenylindole and bisbenzimide (Hoechst 33258). A comparative footprinting study. Biochim Biophys Acta. 1988;949(2):158–168. - PubMed
    1. Lichtman JW, Conchello J-AA. Fluorescence microscopy. Nat Methods. 2005;2(12):910–919. - PubMed
    1. St Croix CM, Shand SH, Watkins SC. Confocal microscopy: comparisons, applications, and problems. BioTechniques. 2005;39(6):S2–S5. - PubMed
    1. Yi M, Kaneko S, Yu DY, Murakami S. Hepatitis C virus envelope proteins bind lactoferrin. Journal of virology. 1997;71:5997–6002. - PMC - PubMed

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