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.
J. Chromatogr. Sci 21, 87-93 (1983). TLC of erucic acid on silica acc. to R.B. LAYER, R. WOOD, J. Assoc. Publ. Analysts 18, 77-89 (1980).
J. Liquid Chromatogr. 6, 1193-1211 (1983). TLC and HPTLC of phospholipids (lecithin, sphingomyelin, phosphatidyl ethanolamine, inositol, serine, glycerol) and lipids (methyloleate, cholesteryl oleate, triolein, cholesterol) on silica with chloroform - ethyl acetate 94:6 and on predeveloped RP-18 with acetonitrile-MK-chloroform - acetic acid 50:30:15:5. Detection with phosphomolybdic acid, cupric acetate, ethanolic sulfuric acid spray reagents. Densitometry.
J. Chromatogr. 292, 473-478 (1984). Isolation of the total egg-yolk phospholipids by the procedure of Bligh-Dyer and the subsequent thin-layer chromatographic separation of the phosphonolipids from the total phospholipids. TLC on silica of phospholipids with methanol - water 2:1 and of phosphonolipids with chloroform - methanol - water 65:25:4. Detection by spraying with iodine, ammonium molybdate, alpha-naphthol-sulphinic acid or ninhydrin.
J. Liquid Chromatogr. 13, 1021-2033 (1990). TLC of lipids and phospholipids on silica with chloroform - methanol - acetic acid - water 68:22:6:4 , and petrol ether - ether - acetic acid 79:20:1. Detection by exposure to iodine vapor for 10 min at room temperature. Quantification by densitometry at 360 nm.
Anal. Biochem. 210, 106-112 (1993). TLC of the radiolabeled neutral glycan fractions of glycosylphosphatidylinositol (GPI) protein anchors and related glycolipids on silica with butanol - ethanol - water 4:3:3, or a combination of 1-propanol - acetone - water 9:6:5 and 5:4:1. Detection by spraying with 20 mg/mL orcinol monohydrate in ethanol - conc. sulfuric acid - water 15:2:1 and heating for 5 min. at 110 °C.
Chinese Anal. Chem. (Fenxi Huaxue) 26, 120 (1998). TLC on silica with benzene - ethyl acetate - acetic acid 240:50:3. Detection under UV 254 nm. Quantification of methyl-, ethyl-, propyl- and butyl-hydroxybenzoates by densitometry at 260 nm. Calculation of the yield for each. Detection limits 100, 100, 200, 300 ng/spot, respectively.
Part I. Comparison of separations of fatty acids on RP-18 plates with and without a concentrating zone. J. Planar Chromatogr. 15, 332-340 (2002). Fatty acids from pentanoic acid to tricosanoic acid have been separated on RP-18 with and without concentrating zone. Visual inspection of the chromatograms revealed that better separation of the acids was obtained on RP-18 plates with concentrating zones because compact chromatographic bands were obtained. TLC of 19 fatty acids on RP-18 with methanol - water 9:1; 19:1 or methanol. Visualization by exposure to iodine vapor.
J. Liq. Chromatogr. Relat. Technol. 30, 2329-2335 (2007). HPTLC of sterols and fatty acids on silica gel (prewashed with methanol) with petroleum ether (36-60 °C) - diethyl ether - acetic acid 80:20:1 in a twin-trough chamber with chamber saturation. Detection by spraying with a 5 % ethanolic phosphomolybdic acid solution followed by heating at 110 °C for 10 min. Quantitative determination by absorbance measurement in the visible range.