This protocol was developed to label proteins in bacterial cells with antibodies conjugated to a fluorophore for fluorescence microscopy imaging. The procedure is optimized to minimize morphological changes and also to minimize the amount of antibodies needed for the staining. The protocol can also be used with primary antibodies conjugated to a fluorophore. The method has been verified extensively (van der Ploeg et al., 2013), but it should be noted that one case in Caulobacter crescentus (Hocking et al., 2012) has been reported in which the localization of a protein changed upon fixation by formaldehyde/glutaraldehyde. However, the localization of the same protein in E. coli did not change
The understanding of how Gram-positive bacteria divide and ensure the correct localization of differ...
Imaging of live cells has been revolutionized by genetically encoded fluorescent probes, most famous...
Antibodies show potential to be used in a variety of applications, but they are difficult to work wi...
International audienceThis protocol was developed to label proteins in bacterial cells with antibodi...
Reliable methods to det. the subcellular localization of bacterial proteins are needed for the study...
Recombinant antibody fragments are emerging as a versatile tool in both basic research and medical t...
There is a need to develop an online bacterial detection system which enables sample preparation, co...
We introduce a non-intrusive method exploiting post-division single-cell variability to validate pro...
Immunofluorescent staining continues to be a crucial technique for determining the cellular localisa...
abstract: The ability to profile proteins allows us to gain a deeper understanding of organization, ...
These continue to be heady times for bacterial cell biology, bothfor experimentalists and formodeler...
Fluorescent markers appropriately conjugated to antibody proteins provide the basis for a method to ...
Confocal fluorescence microscopy and electron microscopy (EM) are complementary methods for studying...
Background Antibody-fluorophore conjugates are invaluable reagents used in contemporary molecular c...
Mol. probes that illuminate the subcellular organization of prokaryotic organisms are essential for ...
The understanding of how Gram-positive bacteria divide and ensure the correct localization of differ...
Imaging of live cells has been revolutionized by genetically encoded fluorescent probes, most famous...
Antibodies show potential to be used in a variety of applications, but they are difficult to work wi...
International audienceThis protocol was developed to label proteins in bacterial cells with antibodi...
Reliable methods to det. the subcellular localization of bacterial proteins are needed for the study...
Recombinant antibody fragments are emerging as a versatile tool in both basic research and medical t...
There is a need to develop an online bacterial detection system which enables sample preparation, co...
We introduce a non-intrusive method exploiting post-division single-cell variability to validate pro...
Immunofluorescent staining continues to be a crucial technique for determining the cellular localisa...
abstract: The ability to profile proteins allows us to gain a deeper understanding of organization, ...
These continue to be heady times for bacterial cell biology, bothfor experimentalists and formodeler...
Fluorescent markers appropriately conjugated to antibody proteins provide the basis for a method to ...
Confocal fluorescence microscopy and electron microscopy (EM) are complementary methods for studying...
Background Antibody-fluorophore conjugates are invaluable reagents used in contemporary molecular c...
Mol. probes that illuminate the subcellular organization of prokaryotic organisms are essential for ...
The understanding of how Gram-positive bacteria divide and ensure the correct localization of differ...
Imaging of live cells has been revolutionized by genetically encoded fluorescent probes, most famous...
Antibodies show potential to be used in a variety of applications, but they are difficult to work wi...