Cumulative CAMAG Bibliography Service CCBS
Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.
The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:
- Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
- Browse and search by CBS classification: Select one of the 38 CBS classification categories where you want to search by a keyword
- Keyword register: select an initial character and browse associated keywords
- Search by CBS edition: Select a CBS edition and find all related publications
Registered users can create a tailor made PDF of selected articles throughout CCBS search – simply use the cart icon on the right hand of each abstract to create your individual selection of abstracts. You can export your saved items to PDF by clicking the download icon.
Anal. Biochem. 171, 248-255 (1988). TLC of lipids on silica with methanol - ethanol - chloroform - NH3 1:49:6:6 or chloroform - methanol - acetic acid - water 60:45:5:3. Visualization by exposing to iodine vapor, by spraying with ninhydrin or molybdate. Chromatograms photocopied on transparent sheets, which are quantified by densitometry.
Anal. Biochem. 175, 167-176 (1988). TLC of lipids from Gaucher’s disease tissue on silica with a) chloroform - methanol - water 65:25:4 and b) chloroform - methanol - water 55:45:10, containing 0.02% Coomassie brilliant blue R. Identification by direct MS analysis.
J. Chromatogr. 483, 369-378 (1989). TLC and circular reversed-phase TLC of ethyl- and 2-chloroethyl esters of fatty acids. and cholesterol esters on silver nitrate-impregnated silica, and on octadecyl-bonded silica with various solvent systems. Detection by spraying with copper(II)sulfate reagent and heating at 100-120°C for 5 min., or by exposure to iodine vapor.
J. Chromatogr. 498, 423-427 (1990). TLC of neutral lipids on silica with 1) ether – benzene – ethanol – triethylamine 40:50:2:1, 2) ether – hexane – triethylamine 10:90:1, 3) ether – hexane – acetic acid 75:25:2 for the tree steps of development. Detection by charring with 95% sulfuric acid.
J. Agric. Food Chem. 39, 451-457 (1991). 2D-TLC of phosphatidyl choline, p-ethanolamine, p-inositol, p-serine, sphingomyelin, cardiolipin, lysophosphatidylcholine and lysophosphatidylethanolamine on silica impregnated with 7.5% magnesium acetate with chloroform - methanol - NH3 5:25:5 (1st dimension) and chloroform - acetone - methanol - acetic acid - water 6:8:2:2:1. Visualization by exposure to iodine vapor, comparison against standard mixture. Quantification after elution using perchloric acid digestion method. TLC analysis of fatty acids acc. to same method; scraping of phospolipids, transmethylation with BF3-methanol in benzene and GC. Thiobarbituric acid assay after TLC.
Chinese Anal. Chem. (Fenxi Huaxue) 19, 733-736 (1991). Two-dimensional TLC of phospholipids on silica with chloroform – methanol – NH3 (28%) 13:7:1 for the first dimension, and chloroform – acetone – methanol – acetic acid 10:4:4:2:1 for the 2nd. Detection by densitometry at 700 nm, and by 31P NMR. Comparison of the two methods.
J. Chromatogr. 615, 142-147 (1993). HPTLC of lipids on silica with 1) chloroform - ethanol - triethylamine - water 30:34:30:8, and 2) hexane ether 50:5 as the initial and final mobile phases, respectively. Detection by spraying with 10 -% copper sulfate in 8% phosphoric acid, and heating to 120 °C. Quantification by densitometry at 310 nm. Detection limit 20 ng/spot.
Biochemical Systematics and Ecology 23, 201-207 (1995). TLC of lipids on silica with hexane - ether - acetic acid 90:10:1. Visualization by spraying with 2,7-dichlorofluorescein solution in ethanol and under UV 360 nm. Purification of the sterol fraction by preparative TLC on AgNO3 - silica 2:8. GC analysis.