The Structures of Tetramethylrhodamine Isothiocyanate Isomers: An N. M. R. Study
作者:
D. Kramer,
H. Klapper,
F. Miller,
期刊:
Spectroscopy Letters
(Taylor Available online 1968)
卷期:
Volume 1,
issue 1
页码: 23-26
ISSN:0038-7010
年代: 1968
DOI:10.1080/00387016808049939
出版商: Taylor & Francis Group
关键词: tetramethylrhodamine;isothiocyanate;n. m. r. study
数据来源: Taylor
摘要:
The use of tetramethylrhodamine isothiocyanate isomers R and G in microbiological and immunochemical procedures has prompted interest in their chemical and physical properties. Tetramethylrhodamine isothiocyanate (TMR) isomer R has been found to be more efficacious than isomer G in immunochemical work (1). Hence, the establishment of the structures of the respective isomers of tetramethylrhodamine isothiocyanates (Figure II) would be of value for better understanding the fluorescent staining and immunochemical activities of these reagents.
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