Talk:Thioflavin

	This article is within the scope of WikiProject Molecular Biology, a collaborative effort to improve the coverage of Molecular Biology on Wikipedia. If you would like to participate, please visit the project page, where you can join the discussion and see a list of open tasks.Molecular BiologyWikipedia:WikiProject Molecular BiologyTemplate:WikiProject Molecular BiologyMolecular Biology articles
???	This article has not yet received a rating on the importance scale.
	This article is supported by the Molecular and Cell Biology task force (assessed as Mid-importance).

Chemicals C‑class Low‑importance

	This article is within the scope of WikiProject Chemicals, a daughter project of WikiProject Chemistry, which aims to improve Wikipedia's coverage of chemicals. To participate, help improve this article or visit the project page for details on the project.ChemicalsWikipedia:WikiProject ChemicalsTemplate:WikiProject Chemicalschemicals articles
C	This article has been given a rating which conflicts with the project-independent quality rating in the banner shell. Please resolve this conflict if possible.
Low	This article has been rated as Low-importance on the project's importance scale.

Untitled

Latest comment: 14 years ago1 comment1 person in discussion

The molecular weight is 318.86 of Thioflavin T (Sigma). Jitendra Well, I have a few questions about this compound and its use, maybe writing them here will serve as a book mark for me to come back and answer them, if no one else does first.

Is Thioflavin T in fact a fluorescent dye? The article discusses the blue shift that is observed upon amyloid binding. Does thsi make the emission appear green? Yellow? Blue? What does unbound dye look like? Are images of dyed amyloids obtained by difference or is the location of the amyloid apparent a stained sample? How long does the stuff stick around in an amyloid aggregate? —Preceding unsigned comment added by Weise (talk • contribs) 22:38, 28 September 2010 (UTC)Reply

Planned update

Latest comment: 13 years ago1 comment1 person in discussion

I am a biophysicist who uses Thioflavin T to study amyloid-forming proteins. The parts of the article dealing with this application of ThT are quite out-of-date. I plan to update this article over the next couple of days with references to recent findings that show how our understanding of this important dye has evolved. Please let me know if you have comments or objections. Ignoramibus (talk) 20:06, 6 May 2011 (UTC)Reply

Mention of benzylamine is erroneous

Latest comment: 8 months ago1 comment1 person in discussion

The following passage is erroneous: "Thioflavin T molecule consists of a benzylamine and a benzothiazole ring connected through a carbon-carbon bond." I think the author who wrote it meant "consists of a para-N,N-dimethylaniline and a benzothiazole..." N,N-dimethylaniline is completely different from benzyl amine. The former molecular fragment has a condensed structural formula of (CH3)2N-C6H4- (consistent with the structure), but the latter has a condensed formula of H2N-CH2-C6H4-. 45.62.183.154 (talk) 17:41, 9 February 2024 (UTC)Reply

Add topic