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.

      102 065
      Phosphoserine aminoacylation of tRNA bearing an unnatural base anticodon
      R. FUKUNAGA, Y. HARADA, I. HIRAO, S. YOKOYAMA* (*Department of Biophysics and Biochemistry, Graduate School of Science, The University of Tokyo, Tokyo, Japan, yokoyama@biochem.s.u-tokyo.ac.jp)

      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 – 66133 for the first dimension and isopropyl alcohol – hydrocloric acid – water 1433 for the second dimension. Quantitative determination by radioactivity measurement of the labeled nucleotides.

      Classification: 21b
      117 078
      Combination nanopreparations of a novel proapoptotic drug – NCL-240, TRAIL and siRNA
      R. RIEHLE, B. PATTNI, A. JHAVERI, A. KULKARNI, G. THAKUR, A. DEGTEREV, V. TORCHILIN* (*Center for Pharmaceutical Biotechnology and Nanomedicine, Department of Pharmaceutical Sciences, Northeastern University, 140 The Fenway, Room 236, 360 Huntington Avenue, Boston, Massachusetts 02115, USA)

      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 41. 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.

      Keywords:
      Classification: 11d, 21b
      66 036
      Combining HPTLC and micro-surface-enhanced Raman spectroscopy (Micro-SERS)
      E. KOGLIN, (Institute of Applied Physical Chemistry, Nuclear Research Center (KFA) Jülich, P.O. Box 1913, D-W-5170 Jülich, Germany)

      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.

      Classification: 4e, 21b
      69 129
      Enzymatic shot-gun 5'-phosphorylation and 3'-sister phosphate exchange
      J.J. STEINBERG*, A. CAJIGAS, M. BROWNLEE, (*Dep. Pathology, Albert Einstein Coll. Med., F-5381300 Morris Park Avenue, Bronx, NY 10461 USA)

      Enzymatic shot-gun 5'-phosphorylation and 3'-sister phosphate exchange a two-dimensional thin-layer chromatographic technique to measure DNA deoxynucleotide modification. 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.

      Classification: 21b
      70 118
      32p-Postlabelling and mass spectrometric methods for analysis of bulky, polyaromatic carcinogen - DNA adducts in humans
      G. TALASKA*, J.G. ROH, T.GETEK, (*Dep. Environ. Health, Univ. Cincinnati, Cincinnati, OH 45267, USA)

      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.

      Classification: 21b
      72 107
      Improved thin-layer chromatographic separation of 32P-postlabeled DNA adducts
      G.G. SPENCER, A.C. BEACH, R.C. PUPTA, (Graduate Center for Toxicol. and Dep. Preven. Med. and Environ. Health, 207 Funkhouser Building, Univ. Kentucky, Lexington, KY 40506-0054, USA)

      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.

      Classification: 21b, 4e
      72 109
      C18 thin-layer chromatographic enhancement of the 32P-postlabeling assay for aromatic or bulky carcinogen-DNA adducts
      M. VIJAYARAJ REDDY, (Environ. & Health Sci. Lab., Mobiloil Corp., P.O. Box 1029, Princeton, NJ 08543-1029, USA)

      C18 thin-layer chromatographic enhancement of the 32P-postlabeling assay for aromatic or bulky carcinogen-DNA adducts Evaluation of adduct recoveries in comparison with nuclease P 1 and butanol methods. 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.

      Classification: 21b
      73 074
      Quantitation of 5-methylcytosine by one-dimensional high-performance thin-layer chromatography
      SH. A. LEONARD, SO CHUN WONG, J.W. NYEE*, (*Dept. Mol. Pharm. & Therapeutics, Sch. Med., East Carolina Univ., Greenville, NC 27858, USA)

      J. Chromatogr. 645, 189-192 (1993). HPTLC of DNA 5-methylcytosine on alkyl amino modified silica with isobutyric acid - water - NH3 17783. Detection under UV 254 nm. Quantification by scintillation counting. Comparison with traditional two-dimensional procedure on polyethyleneimine cellulose and HPLC method.

      Classification: 21b