Cite as: Cold Spring Harb. Protoc.; 2007; doi:10.1101/pdb.prot4797

This Protocol
Right arrow Full Text
Right arrow Update/discuss this protocolDiscussion icon
Right arrow Alert me when this protocol is cited
Right arrow Alert me when comments are published
Right arrow Alert me if a correction is posted
Services
Right arrow Similar protocols in this database
Right arrow Alert me to new releases of protocols
Right arrow Save to Personal Folders
Right arrow Download to citation manager
Right arrow Printer-friendly versionPrinter-friendly version
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Blair, S. S.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Blair, S. S.
Related Collections
Right arrow Cell Biology, general
Right arrow Genetics, general
Right arrow Imaging Development
Right arrow Laboratory Organisms, general
Right arrow Drosophila
Right arrow Molecular Biology, general
Right arrow Analysis of Gene Expression
Right arrow Analysis of Gene Expression, general
Right arrow Drosophila Transgenics
Right arrow Immunohistochemistry
Right arrow Developmental Biology
Right arrow Immunostaining
Right arrow Immunostaining, general
Right arrow Immunostaining Tissues
Right arrow Visualization of Gene Expression
Right arrow Use of Reporter Genes
Right arrowRelated Protocols
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
BSN globe

protocolProtocol

Nickel-Intensified ABC-HRP Antibody Staining of Imaginal Discs in Drosophila

Seth S. Blair

This protocol was adapted from "Imaginal Discs," Chapter 10, in Drosophila Protocols (eds. Sullivan et al.). Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2000.


INTRODUCTION

This protocol describes a sensitive method for labeling Drosophila imaginal disc tissues with a single antiserum. Labeling is visualized using a nickel-intensified avidin/biotinylated enzyme complex-horseradish peroxidase (ABC-HRP) staining procedure. This method is more sensitive, and has a lower signal-to-noise ratio, than fluorescent labeling. Although these methods are useful for visualizing genetic mosaic clones in wandering larval stage imaginal discs and pupal tissues from Drosophila, the immunohistological techniques are generally applicable to the description of protein expression.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?

Related Protocols

Generating Imaginal Disc Clones in Drosophila
Seth S. Blair
CSH Protocols 2007: 4793. [Abstract] [Full Text]

Dissection of Imaginal Discs in Drosophila
Seth S. Blair
CSH Protocols 2007: 4794. [Abstract] [Full Text]

Fixation of Imaginal Discs in Drosophila
Seth S. Blair
CSH Protocols 2007: 4795. [Abstract] [Full Text]

Triple-Label Fluorescent Antibody Staining of Imaginal Discs in Drosophila
Seth S. Blair
CSH Protocols 2007: 4796. [Abstract] [Full Text]