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. The saved items can be printed to PDF using the print function of your web browser.
Biochem. Biophys. Res. Commun. 372, 480-485 (2008). 2D-TLC of alpha-32P ATP or alpha-32P UTP labeled nucleotides after RNase T2 treatment of tRNA transcripts synthesized by T7 RNA polymerase, on silica gel with isobutyric acid – ammonia – water – 66:1:33 for the first dimension and isopropyl alcohol – hydrocloric acid – water 14:3:3 for the second dimension. Quantitative determination by radioactivity measurement of the labeled nucleotides.
Pharm. Res. 33, 1587-1601 (2016). HPTLC study of the cleavability of the disulfide bond in a conjugate siRNA-S-S-PE (incubated in 10 mM glutathione at 37 °C for 4 h) on silica gel with chloroform – methanol 4:1. Detection by spraying with molybdenum blue dye for the cleaved phospholipids. This test confirmed the potential utility of this system for siRNA delivery in vivo.
J. Planar Chromatogr. 2, 194-197 (1989). Discussion of a new method for preparing surface-enhanced Raman spectroscopy using silver colloidal spheres deposited on HPTLC plates. The sensitivity permits the aquisitation of Raman spectra from HPTLC spots down to 1 µm in size. It is possible to identify organic substances in the pico- and femtogram region of mass.
J. Chromatogr. 574, 41-55 (1992). Two-dimensional TLC of DNA adducts, labeled by shot-gun 5'-phosphorylation of representative 32P-a-deoxyribonucleotide monophosphates, on PEI cellulose with 0.1 M acetic acid (pH 3.5) for the first dimension and 5.6 M (NH4)2SO4, 0.12M Na2EDTA, and 0.035M (NH4)HSO4 (to pH 4) for the second at temperature of 17°C, 50-60% humidity constant. The technique quantifies low-molecular - mass adducts and DNA integrity both in vivo and in vitro.
J. Chromatogr. 580, 293-323 (1992). Discussion of 32p-postlabelling technique as a human carcinogen - DNA adduct biomonitoring method, involving enzymatic preparation and labelling of DNA samples, followed by TLC and HPLC separation of carcinogen - nucleotide adducts from unadducted nucleotides. Use of both synchronous fluorescence and HPLC in conjunction with 32p-postlabelling and TLC to confirm the identity of specific carcinogen DNA adducts in human samples.
J. Chromatogr. 612, 295-301 (1993). TLC of 32P-postlabeled DNA adducts on polyethyleneimine-cellulose with different mobile phases. Detection by intensifying screen-enhanced autoradiography. Quantification by Cerenkov counting with adducts expressed in counts per minute. Discussion of the separation, resolution, recovery, retention of background noise, and developing time.
J. Chromatogr. 614, 245-251 (1993). Investigation of the suitability of RP-18 TLC for enhancement of adducts in the 32P-postlabeling assay, for structurally diverse classes of DNA adducts derived from benzo[a] pyrene, 2-acetylaminofluorene, benzoquinone, sarfrole, and mitomycin C. Retention of adducts to C18 phase followed by elution with organic solvent - water. Comparison of adduct recoveries with those obtained by nuclease P1 and butanol methods.
J. Chromatogr. 645, 189-192 (1993). HPTLC of DNA 5-methylcytosine on alkyl amino modified silica with isobutyric acid - water - NH3 177:8:3. Detection under UV 254 nm. Quantification by scintillation counting. Comparison with traditional two-dimensional procedure on polyethyleneimine cellulose and HPLC method.