Chromosomal FISH-TSA: Difference between revisions
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Created page with "Literature: Krylov V., Macha J., Tlapakova T., Takac M., Jonak J. (2003) The c-SRC1 gene visualized by in situ hybridization on Xenopus laevis chromosomes. Cytogenet. Genome Res..." |
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Literature: | '''Literature:''' | ||
Krylov V., Macha J., Tlapakova T., Takac M., Jonak J. (2003) The c-SRC1 gene visualized by in situ hybridization on Xenopus laevis chromosomes. Cytogenet. Genome Res. 2003;103(1-2):169-172. [http://www.ncbi.nlm.nih.gov/pubmed/15004482]. | Krylov V., Macha J., Tlapakova T., Takac M., Jonak J. (2003) The c-SRC1 gene visualized by in situ hybridization on Xenopus laevis chromosomes. Cytogenet. Genome Res. 2003;103(1-2):169-172. [http://www.ncbi.nlm.nih.gov/pubmed/15004482]. | ||
Tlapakova T., Krylov V., Macha J. (2005) Localization, structure and polymorphism of two paralogous Xenopus laevis mitochondrial malate dehydrogenase genes. Chromosome res. 13(7):699-706. [http://www.ncbi.nlm.nih.gov/pubmed/16235119]. | |||
Krylov V., Tlapakova T., Macha J. (2007) Localization of Mdh2 single copy gene on Xenopus tropicalis chromosomes by FISH-TSA technique. Cytogenet. Genome Res. 116:110-112. [http://www.ncbi.nlm.nih.gov/pubmed/17268187]. | |||
Following protocol is designed for the visualization of short cDNA sequences with the minimal lenght of 900-1000 bp. | |||
'''Protocol:''' | |||
* [[Image:Krylov_FISH-TSA_protocol.pdf |Data mapping document]] | |||
Latest revision as of 15:43, 10 January 2011
Literature:
Krylov V., Macha J., Tlapakova T., Takac M., Jonak J. (2003) The c-SRC1 gene visualized by in situ hybridization on Xenopus laevis chromosomes. Cytogenet. Genome Res. 2003;103(1-2):169-172. [1].
Tlapakova T., Krylov V., Macha J. (2005) Localization, structure and polymorphism of two paralogous Xenopus laevis mitochondrial malate dehydrogenase genes. Chromosome res. 13(7):699-706. [2].
Krylov V., Tlapakova T., Macha J. (2007) Localization of Mdh2 single copy gene on Xenopus tropicalis chromosomes by FISH-TSA technique. Cytogenet. Genome Res. 116:110-112. [3].
Following protocol is designed for the visualization of short cDNA sequences with the minimal lenght of 900-1000 bp.
Protocol: