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
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VIII. Separation of l-o-acetylethylene glycol-2-(2-trimethyl-ammonium-ethyl) and -(2-aminoethyl) phosphonates from their phosphoryl analogues and other phosphonolipids. J. Chromatogr. 351, 376-378 (1986). TLC of l-o-acetylethylene glycol-2-(2-trimethyl-ammoniumethyl) and-(2-aminoethyl) phosphonates on silica with a) chloroform - methanol - water 65:25:4, b) methanol - water 2:1. Detection by exposure to iodine vapor, or UV irradiation, or spraying with molybdenum blue.
H. TRAITLER, A. STUDER, R.E. KAISER (eds): Instrumental HPTLC, Institute for Chromatography, Bad Dürkheim, FRG (1987), 101-109. TLC of phospholipids and glycolipids on silica with chloroform - methanol - triethylamine - water 30:35:34:8 and chloroform - methanol - 0.25% calcium chloride 60:35:8, resp. Detection by dipping in TNS reagent and photographing on film negatives. Measurement by laser scanning in transmittance mode. Detection limit, 25 ng.
J. Chromatogr. 409, 291-7 (1987). TLC on 5% silver nitrate-impregnated silica developed to 3 cm above the origin with chloroform - methanol - water 70:30:4, and to 16 cm with chloroform - methanol - water 90:10:1. Analysis by enzymatic radioacitve phosphorylation.
J. Chromatogr. 426, 188-193 (1988). TLC of 6 neutral glycosphingolipids on silica with 4 solvent systems composed of isopropanol, 15M NH3, methyl acetate and water. Detection by spraying with 50% sulfuric acid and heating at 110°C.
Anal. Biochem. 173, 10-17 (1988). HPTLC on silica with acetone - 5N NH3 50:0.9. Detection by autoradiography. Liquid scintillation, spectrometry after scraping. Fixation of the silica gel and treatment with neuraminidase from Vibrio cholerea in the absence of detergent and incubation of the plates with antibodies. Visualization of bound first antbodies by using alkaline phosphatase conjugated second antibodies. Detection limit, 30 ng.
J. Liquid Chromatogr. 12, 3151-3161 (1989). TLC of sterols and other lipids on silica with isopropyl ether – acetic acid 96:4, followed by hexane – ether – acetic acid 90:10:1. Detection of lipids by spraying with 5% ethanolic phosphomolybdic acid and heating for 5-10 min at 100-120°C. Semiquantification by comparison of the zone sizes and intensities of standards and samples. Quantification of cholesterol by densitometry after development with chloroform – ethyl acetate 96:4, and dipping in cupric acetate – phosphoric acid reagent and heating at 100°C. Quantification of triacylglycerols and free fatty acids by densitometry after development with hexane – ether – acetic acid 80:20:1, followed by spraying with cupric acetate – phosphoric acid reagent. Also GC.
Chromatographia 30, 414-420 (1990). HPTLC of ether phospholipids on silica with ten different solvents. Detection by dipping in cupric sulfate - phosphoric acid and manganese chloride - sulfuric acid , or 1-anilino-8-naphthalene sulfonate. Test of two lipophilic fluorescence reagents which move in mobile phase. Detection limits, ng level. Discussion of characteristics of sorbents and influence of NBD-dihexadecylamine fluorescence detection method. Quantification by densitometry.
J. Liquid Chromatogr. 14, 3259-3267 (1991). TLC of neutral lipids on silica with petrol ether – ether – acetic acid 40:10:1. Detection by spraying with PMA reagent. Discussion of the differences in the neutral lipid profiles and the factors in determining the lipid composition of the snail.