The Yeast HA-tagged strains have random, in-frame affinity tags created with minitransposons. Insertion of the HA-tag via mini-transposon (mTn) mutagenesis allows for tagging within the coding region of the protein in a non-biased fashion, resulting in the tagging of both annotated and previously unidentified ORFs.
The HA insertion potentially provides several means by which yeast protein function may be studied. HA-tagged yeast proteins have been used effectively in large-scale studies of protein localization. Full-length HA tagged proteins can be localized to the appropriate cellular region where they can be detected using an antibody to the HA epitope.
Native amounts of protein can easily be purified from individual yeast strains using immunoprecipitation with a commercially available HA antibody. Also, HA insertion may potentially generate conditional alleles and hypomorphic mutants that exhibit partial gene function of particular importance in the analysis of essential genes.
- Collection contains over 2400 yeast mutagenized strains
- Generate HA epitope tagged proteins for immunolocalization or immunoprecipitation using antibodies against HA
- A potential source of conditional alleles and hypomorphic mutants (generated by transposon insertion of 3 x HA Tag)
- The HA-Tagged Yeast Collection is provided in a diploid ura3 leu2 background
Strains are not guaranteed to produce a fully functional protein, and complete analysis is to be performed by the individual researcher. Information on strains that have been successfully immunolocalized is available on the TRIPLES website.
We provide certain clone resources developed by leading academic laboratories. Many of these resources address the needs of specialized research communities not served by other commercial entities. In order to provide these as a public resource, we depend on the contributing academic laboratories for quality control.
Therefore, these are distributed in the format provided by the contributing institution "as is" with no additional product validation or guarantee. We are not responsible for any errors or performance issues. Additional information can be found in the product manual as well as in associated published articles (if available). Alternatively, the source academic institution can be contacted directly for troubleshooting.
Individual strains are provided as a live culture in a 2 mL tube. Each tube contains YPAD broth supplemented with 15% glycerol. Store the strain at 4°C for up to one week or -80°C indefinitely.
Bulk orders are shipped as glycerol stocks in 96-well microtiter plates and are a culture of the HA–Tagged Yeast in YPAD media and glycerol. These plates ship on dry ice and can be maintained indefinitely at -80°C.
- P. Ross-Macdonald, et.al., Large-scale analysis of the yeast genome by transposon tagging and gene disruption. Nature 402(6760), 413-418 (25 November 1999).
- A. Kumar et. al., Subcellular localization of the yeast proteome. Genes & Development. 16(6), 707-719 (15 March 2002).
- A. Kumar et al., TRIPLES: a database of gene function in Saccharomyces cerevisiae. Nucleic Acids Res. 28(1), 81-84 (1 January 2000).