High impact information on Cyanin

• We compared the detection of bacteria and archaea in the coastal North Sea and at Monterey Bay, Calif., after fluorescence in situ hybridization (FISH) either with rRNA-targeted oligonucleotide probes monolabeled with the cyanin dye Cy3 (oligoFISH) or with fluorescein-labeled polyribonucleotide probes (polyFISH) [1].
• Changes in membrane potential, using the cyanin dye method, also indicated that most of these drugs cancelled functional changes of plasma membrane of PMNs [2].
• Fluorescence properties, thermal duplex stability, and kinetics of formation of cyanin platinum DNAs [3].
• Neurotensin- and EGF-induced phosphorylation of ERKs was not affected by cyanidin, cyanin, and idaein at < or = 100 microM [4].
• Cyanidin, but not cyanin and idaein, was able to inhibit an increase in intracellular Ca2+ concentration induced by neurotensin [4].

Biological context of Cyanin

• We also analyzed the kinetics of the reaction of the cyanin platinum compounds with DNA [3].
• Array comparative genomic hybridization with cyanin cis-platinum-labeled DNAs [5].

Anatomical context of Cyanin

• Sections were stained with one of the above histochemical procedures and adjacent sections were stained with Solachrome cyanin , which differentially stains nerve elements from muscle fibers [6].
• The solochrome cyanin stain for myelin was also applied [7].
• A tibial nerve from a disease-arrested borderline tuberculoid (BT) leprosy patient was dissected out and examined almost in its entirety using hematoxylin and eosin staining, a modified Fite's stain for acid-fast bacilli (AFB), solochrome cyanin stain for myelin, and van Gieson's stain for fibrous tissue [8].

Associations of Cyanin with other chemical compounds

• Only cyanidin (100 microM), but not cyanin and idaein, was able to inhibit cellular growth induced by EGF [4].
• Bioflavonoids extracted from red soybeans are mostly cyanin conjugated with glucose and rhamnose, whereas bioflavonoids of red beans are cyanin conjugated with rhamnose as revealed by thin-layer chromatogram [9].

Gene context of Cyanin

• Stains for EGF, GFAP, NP and solochrome cyanin were negative [7].
• Cyanidin (10 microM), but not its glycosides cyanin and idaein, was able to inhibit the neurotensin- and EGF-induced increased rate of extracellular acidification [4].
• Following two-color cyanin dye labeling and hybridization of subtracted tester with either unsubtracted driver or unsubtracted tester cDNAs to the SSH libraries arrayed on glass slides, two values were calculated for each clone, an enrichment ratio 1 (ER1) and an enrichment ratio 2 (ER2) [10].

Analytical, diagnostic and therapeutic context of Cyanin

• Where appropriate, parallel samples were labeled with other fluorochromes (including R-PE, APC, the cyanin dyes Cy3 and Cy5, and others) to gauge the performance of the cryptomonad fluorochromes against fluorescent labels previously evaluated for flow cytometry [11].

References