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Merck
CN

Immunofluorescence Microscopy of the Mammalian Golgi Apparatus.

Methods in molecular biology (Clifton, N.J.) (2022-12-14)
Maryam Arab, Sanjeev Chavan Nayak, Teresa Vitali, Martin Lowe
摘要

Immunofluorescence is a technique that uses antibodies and fluorophores to label structures inside cells. The cells are normally fixed and permeabilized, and then structures are labelled using primary antibodies directly conjugated to fluorophores, or, more commonly, first with an antibody against an antigen of interest followed by a secondary antibody conjugated to a fluorophore that binds to the primary antibody. Fluorescence can be visualized using widefield, confocal, or super-resolution microscopy. Here we focus on labelling of the Golgi apparatus and show that different fixation and permeabilization conditions can significantly affect labelling of Golgi proteins and describe how to optimize fluorescent detection of Golgi proteins.

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Monoclonal Anti-β-COP antibody produced in mouse, clone M3A5, ascites fluid
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Anti-TRIP11 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution