Improved method for detection of cellular transcripts by in situ hybridization

1983 ◽  
Vol 77 (1) ◽  
pp. 123-131 ◽  
Author(s):  
C. M. Godard
Keyword(s):  
In Situ Hybridization ◽  
Improved Method

An improved method for whole-mount in situ hybridization of Heterodera schachtii juveniles

2002 ◽  
Vol 88 (8) ◽  
pp. 731-733 ◽  
Author(s):  
Bartel Vanholme ◽  
Jan De Meutter ◽  
Tom Tytgat ◽  
Greetje Gheysen ◽  
Isabelle Vanhoutte ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Heterodera Schachtii ◽  
Improved Method ◽  
Whole Mount

An improved method for G-banding chromosomes after in situ hybridization

1984 ◽  
Vol 38 (4) ◽  
pp. 308-309 ◽  
Author(s):  
L.A. Cannizzaro ◽  
B.S. Emanuel
Keyword(s):  
In Situ Hybridization ◽  
Improved Method

scholarly journals Improved Method of Detecting the ERG Gene Rearrangement in Prostate Cancer Using Combined Dual-Color Chromogenic and Silver In Situ Hybridization

2012 ◽  
Vol 14 (4) ◽  
pp. 322-327 ◽  
Author(s):  
Martin Braun ◽  
Julia Stomper ◽  
Diana Boehm ◽  
Wenzel Vogel ◽  
Veit J. Scheble ◽  
...  
Keyword(s):  
Prostate Cancer ◽  
In Situ Hybridization ◽  
Gene Rearrangement ◽  
Improved Method ◽  
Dual Color ◽  
Silver In Situ Hybridization

DNA sequence mapping in interphase and metaphase chromosomes by fluorescence in situ hybridization

1992 ◽  
Vol 50 (1) ◽  
pp. 496-497
Author(s):  
Barbara Trask ◽  
Susan Allen ◽  
Anne Bergmann ◽  
Mari Christensen ◽  
Anne Fertitta ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Dna Sequence ◽  
Dna Sequences ◽  
Dual Band ◽  
Nick Translation ◽  
Metaphase Chromosomes ◽  
Band Pass ◽  
Texas Red ◽  
Fluorescent Spot

Using fluorescence in situ hybridization (FISH), the positions of DNA sequences can be discretely marked with a fluorescent spot. The efficiency of marking DNA sequences of the size cloned in cosmids is 90-95%, and the fluorescent spots produced after FISH are ≈0.3 μm in diameter. Sites of two sequences can be distinguished using two-color FISH. Different reporter molecules, such as biotin or digoxigenin, are incorporated into DNA sequence probes by nick translation. These reporter molecules are labeled after hybridization with different fluorochromes, e.g., FITC and Texas Red. The development of dual band pass filters (Chromatechnology) allows these fluorochromes to be photographed simultaneously without registration shift.

Ultrastructural analysis of the spatial distribution of MRNA

1992 ◽  
Vol 50 (1) ◽  
pp. 552-553
Author(s):  
Gary Bassell ◽  
Robert H. Singer
Keyword(s):  
Electron Microscopy ◽  
Spatial Distribution ◽  
In Situ Hybridization ◽  
High Resolution ◽  
Nucleic Acids ◽  
Colloidal Gold ◽  
Dna Probe ◽  
Nucleotide Analogs ◽  
Gold Particles

We have been investigating the spatial distribution of nucleic acids intracellularly using in situ hybridization. The use of non-isotopic nucleotide analogs incorporated into the DNA probe allows the detection of the probe at its site of hybridization within the cell. This approach therefore is compatible with the high resolution available by electron microscopy. Biotinated or digoxigenated probe can be detected by antibodies conjugated to colloidal gold. Because mRNA serves as a template for the probe fragments, the colloidal gold particles are detected as arrays which allow it to be unequivocally distinguished from background.

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