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.

      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: 4e, 21b
      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)

      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 177:8:3. Detection under UV 254 nm. Quantification by scintillation counting. Comparison with traditional two-dimensional procedure on polyethyleneimine cellulose and HPLC method.

      Classification: 21b
      76 103
      Comparison of TLC- and HPLC- 32P-postlabelling assay for cisplatin-DNA adducts
      A. FOERSTI, J. STAFFAS, K. HEMMINKI, (Cent. Nutrition Toxicol., Karolinski Inst., S-14157 Huddinge, Sweden)

      Carcinogenesis 15, 2829-2834 (1994). Separation of the title compounds, postlabelled with [g-32P] ATP, by TLC and HPLC with on-line detection of 32P.

      Keywords:
      Classification: 21b, 34
      76 216
      Pulsed field gel electrophoresis labelling method to study the pattern of saccharomyces cerevisiae chromosomal DNA synthesis during the G1/S phase of the cell cycle
      A.Y. JONG, B. WANG, SH. Q. ZHANG, (Dept. Pediatrics & Microbiol. Univ. Southern California Sch. Med., Los Angeles, California 90033, USA)

      Anal. Biochem. 227, 32-39 (1995). Presentation of the title method for investigating the yeast chromosomal DNA synthesis by first labelling yeast cells with 32P in vivo, then resolving chromosomal DNA molecules the PFGE. Discussion of the mechanism of the method. Demonstration of the quantification of DNA.

      Keywords:
      Classification: 21b, 36
      80 059
      In vivo determination of 5-bromo-2'-deoxyuridine incorporation into DNA tumor tissue by a new 32P-postlabelling thin-layer chromatographic method
      J.J. STEINBERG*, G.W. OLIVER Jr., N. FARAH, P. SIMONI, R. WINIARSKY, A. CAJIGAS, (*Unified Div. Autopsy, Dept. Pathol. & Radi. Oncol., Albert Einstein Coll. Med., Montefiore Med. Cent., C-312, III East 210th St., Bronx, New York, NY 10467, USA)

      J. Chromatogr. B 694, 333-341 (1997). 2D-TLC on PEI-cellulose with acetic acid, (NH4)2SO4 and (NH4)HSO4. Use of the method to measure DNA chemotherapy analogue accumulation in tumor. The method may offer an additional biomarker of tumor cell drug resistance and host sensitivity which may affect the chemotherapeutic regimen.

      Keywords:
      Classification: 21b
      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 – 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.

      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 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.

      Classification: 11d, 21b