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. Liq. Chrom. & Rel. Technol. 24, 1511-1514 (2001). TLC of a peptidoglycan monomer (PGM) (GlcNAc-MurNAc-L-Ala-D-isoglutaminyl-meso-diamino-pimelyl-D-Ala-D-Ala), some metals and their complexes on cellulose with n-propanol - NH3 - water 7:3:1 and n-butanol - ethyl acetate - acetic acid - water 1:1:1:1. Detection of the metal complexes by e.g. dipping the plate in a 0.25% solution of (1-(2-pyridylazo-2-naphthol)) in ethanol. Detection of PGM by dipping in 0.2% ethanolic ninhydrin solution and heating at 110°C.
Biochem. Biophys. Res. Commun. 487, 702-708 (2017). HPTLC of the reaction products of different 14C-labeled substrates of the mevalonate pathway (MVA, MVA-5-P, MVA-3-P, MVA-5-PP) and the recombinant Flavobacterium johnsoniae protein on silica gel with n-propanol – 28 % ammonia – water 6:3:1. The distribution of radioactivity on the TLC plate was detected using a suitable image analyzer.
J. Chromatogr. 387, 551- 555 (1987). HPTLC of toxic peptides from different microcystis aeruginosa strains on RP-18 with chloroform - methanol 1:1 or 2:1 and on silica with dichloromethane - methanol 2:3 or chloroform - methanol 3:1. The toxins appeared as pale blue-white spots under UV. Prior to HPTLC, the toxin extracts were purified on C18 Sep-Pak cartridges with methanol.
J. of Medicinal Chemistry 32, 174-179 (1989). TLC on silica with 1-butanol - acetic acid - pyridine - water 5:5:4:1, 2-propanol - 25% NH3 - water 3:1:1, ethyl acetate - pyridine - acetic acid - 5:5:1:3 and butanol - acetic acid - water 4:1:5. Visualization with ninhydrin, fluorescamine and iodine vapor.
J. of Medicinal Chemistry 32, 880-884 (1989). TLC of peptides on silica with butanol - ethyl acetate - acetic acid - water 1:1:1:1 and butanol - acetic acid - water 4:1:5. Visualization with 10% bleach-1% KI-starch.
J. Peking Univ. (Beijing Daxue Xuebao) 28, 178-184 (1992). Determination of the RM values of a series of dermorphin - related oligopeptides by TLC. Discussion of the influence of the functional group on RM values.
CBS 85, 4-5 (2000). HPTLC of peptide fragment A on lichrospher silica gel with dichloromethane over 50 mm. Quantitative determination by absorbance measurement at 250 nm. Precision is 0.23 % (n=10 at 50 ng) and repeatability 2.9 % (n=30 over 5 plates at 50 ng), recovery is found to be 104 % at 50 ng.
J. Planar Chromatogr. 30, 375-385 (2017). HPTLC of synthetic peptides on silica gel and RP-18 with water and methanol with the addition of proper ion-pairing reagent to study the influence of metallic impurities on the retention and efficiency of separation of peptides. Detection by dipping into 2 % ninhydrin solution in acetone ‒ methanol ‒ glacial acetic acid 25:25:2. The contents of trace elements in areas scraped off from the chromatographic plates were determined by flame technique of atomic absorption spectrometry. The impurities present in the adsorbents may cause characteristic disruption of solute zone shape and overall distortion of the chromatogram during the development.