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. 382, 308-313 (1986). TLC of 5 phospholipids, 5 neutral lipids, 4 cholesterol ester subfractions on silica with 2 successive runs with chloroform - methanol - water 65:25:4 and n-hexane - acetone 100:1. Analysis of lipids in human blood.
Chinese Anal. Chem. 15, 748-750 (1987) (Fenxi Huaxue). TLC of mono-, di-, tri- glycerol stearates on silica with cyclohexane - chloroform - THF 85:25:20. Detection by exposing to iodine vapor. Quantification by densitometry at 420 nm. RSD 1.2-2.7%
J. Chromatogr. 439, 453-458 (1988). TLC of lipids on silica with chloroform - methanol - water 65:25:4. Detection by exposure to iodine vapor or spraying with molybdenum blue reagent.
J. Chromatogr. 462, 467-470 (1989). TLC of cholesteryl acetate and its chloro analogues on silica with hexane - ethyl acetate 4:1, 9:1, 19:1, 24:1 and 66:1. Detection by spraying with 50% sulfuric acid and heating at 120°C for 5 min. Also HPLC.
A limited phylogenetic study. J. Chromatogr. 525, 339-347 (1990). One and two dimensional TLC of myelin lipids on silica with a) chloroform - methanol - water 70:24,5:2.7, b) chloroform - methanol 9:2, c) chloroform - ethyl acetate 3:5. Investigation of the selective staining by thionine, interpreted by a preceding primary alkylamine 0-deacylation step.
J. Planar Chromatogr. 2, 207-210 (1989). Investigation of the role of phospholipid-derived second-messengers in B-cell signal transduction with a system which allows the simultaneous detection of lipids from a wide rage of polarity as well as low limits of determination. Using a monophasic lipid extraction (hexane-isopropanol (3+2) and separation of the anionic from the zwitterionic and neutral lipids by anion-exchange chromatography with subsequent desalting, 18 different lipids (or groups of lipids) from one single extract could be separated by straight-phase HPTLC (N-chamber; chloroform – methanol – trimethylenamine- water 30:35:34:8). Detection by dipping into cupric sulfate reagent and heating at 175°C for 10 min. The cupric sulfate reagent is much more stable than molybdenum blue. In situ quantification is a powerful tool to investigate small biological samples. This sensitivity compares well with recently published HPLC methods.
Chem. Anal. (N.Y.) 108, 59-68 (1990). A review with 32 references on TLC-immunostaining as a method for identification and characterization of glycolipids as well as anti-glycolipid antibodies, using silica as a site where reactions, such as degradative or biosynthetic reactions of glycolipids can proceed.
J. Chromatogr. 588, 295-301 (1991). HPTLC of 21 different lipids on silica with a) carbon tetrachloride, b) chloroform - methanol - methyl acetate - water 25:16:4:2, and c) chloroform - ethyl acetate 94:6. Detection by immersion for 10 sec in a tank of 0.25 nM hematoporphyrin followed by rinsing with water, and immersion for 10 sec in a 10 mM solution of copper(II)nitrate, and heating at 100 °C for 5 min. Detection limit in the low nanogram range. Investigation of visual detection limits, selectivity and photostability of hematoporphyrin.