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.
(Hungarian). Elelmezesi Ipar 43, 399-408 (1989). TLC of oleic, linolic and linolenic acids on silica with petrol ether - diethyl ether - acetic acid 80:20:1. Visualization by spraying with 5% phosphomolybdic acid in 96% ethanol.
J. of Natural Products 53, 1015-1018 (1990). Preparative TLC on silica with chloroform – methanol – NH3 7:3:0.5, followed by preparative TLC on RP-18 silica with methanol – water 4:1. Also purification of the acetylated derivatives by preparative TLC on silica with chloroform – methanol – water 20:3:0.5.
Proc. 6th Int. Symp. Instrum. Planar Chromatogr., (Interlaken 1991), Inst. Chromatogr., Bad Dürkheim, FRG, 49-55 (1991). Separation of ceramides and cholesterol on silica, using a four-step 2-D developing technique: first direction with chloroform - acetone - methanol 90:5:5 over 1 cm, second direction with the same solvent over 8.5 cm, then in the first direction again with chloroform - acetone - methanol - NH3 60:30:8:2, and finally with chloroform - acetone - methanol - acetic acid - water 78:16:4:2:1 in the second direction. Derivatization by dipping in phosphoric acid - acetic acid - sulfuric acid - water 10:10:1:180 followed by heating at 200 °C for 10 min. Method for routine analysis of ceramides.
Anal. Biochem. 192, 281-292 (1991). Multiple-development TLC of lipids on silica impregnated with boric acid. Neutral lipids separated with ether; 1,2-diacylglycerols with benzene - hexane - ether - formic acid 325:250:10:2. TLC of cellular phosphatidate and phosphatidylethanol on silica with benzene - chloroform - pyridine - formic acid 45:38:4:2. Detection by spraying with CuSO4 in 10 % H3PO4 and heating at 180 °C for 20 min. Quantification by densitometry (absorbance at 400 nm); detection limits 50 pmol.
J. China Assoc. Instr. Anal. (Fenxi Ceshi Tongbao) 11, 74-77 (1992). TLC of the composition of protein and lipid in chemically modified keratin fibers on silica with chloroform - methanol 80:2. Detection by exposure to iodine vapor. Also polyacrylamide gel electrophoresis.
Nippon Shokubutsu Byori Gakkaiho (Jap. Bulletin Plant Pathol. 59, 528-534 (1993). TLC of lipids on silica with 1) chloroform - methanol 2:1 and 2) with chloroform - methanol - water 60:25:4. Detection by spraying with ninhydrin and heating. Comparison of the chromatograms of different bacteria isolates at the generic level and at the species level in the cases of Erwinia and Psudomonas.
J. Planar Chromatogr. 9, 379-381 (1996). HPTLC of cholesterol, phosphatidylethanolamine, phosphatidylcholine, and lysophosphatidylcholine on silica with chloroform - methanol - water 65:25:4 after prewashing with chloroform - methanol 1:1. Quantification by densitometry at 370 nm.
J. Planar Chromatogr. 11, 47-50 (1998). HPTLC of lipids (cholesterol, oleic acid, triolein, methyl oleate, cholesteryl oleate as standard) on silica gel with hexane - ether - acetic acid 40:10:1. After drying at 115°C for approx. 15 min the lipids were detected as blue spots on a yellow background by spraying with 5% ethanolic phosphomolybdic acid and heating for 15 min at 115°C. Quantitation by densitometry at 700 nm.