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.

      78 079
      Affinity purification of phospholipase A2 on immobilized artificial membranes containing and lacking the glycerol backbone
      C. BERNAL, CH. PIDGEON*, (*Dept. Med. Chem., Sch. Pharm., Purdue Univ., West Lafayette, IN 47907, USA)

      J. Chromatogr. A 731, 139-151 (1996). SDS-PAGE of proteins collected from the immobilized artificial membrane column. Detection by scanning densitometry at 400 nm for the silver-stained 15 % polyacrylamide gel. Measurement of the protein contents by using bicinchoninic (BCA) protein assay kit. Qualitative assay of phospholipase Az by color reaction, and quantification with radioactive method. Discussion of the use of IAMs to develop purification methods for the enzymes obtained from diverse biological specimens.

      Keywords:
      Classification: 20, 36
      122 052
      Monoacylglycerol and diacylglycerol production by hydrolysis of refined vegetable oil by-products using an immobilized lipase from Serratia sp
      Z. ZIED*, A. EDAHECH, F. RIGANO, G. MICALIZZI, L. MONDELLO, N. KHARRAT, M. SELLAMI, F. CACCIOLA (*Laboratory of Biochemistry and Enzymatic Engineering of Lipases, National School of Engineers of Sfax, University of Sfax, PB 1173, Km 4 Soukra Road, Sfax, Tunisia, zaraizied@hotmail.fr)

      W3. J. Sep. Sci. 41, 4323-4330 (2018). HPTLC of monoacylglycerol (MAGs) and diacylglycerol (DAGs) in byproducts of refined vegetable oils by hydrolysis and esterification with glycerol using a new microbial immobilized lipase from Serratia sp. W3 (LSm) and Candida Antarctica lipase on silica gel with hexane – diethyl ether – acetic acid 180:20:1. Detection by exposure to iodine. The TLC analysis showed that the LSm enhanced the formation of MAGs and DAGs leading to a practically complete hydrolysis of refined vegetable oil by-products.

      Classification: 11c, 20
      78 080
      An HPTLC method for the assay of UDP-glucuronosyltransferase using p-nitrophenol as substrate
      P. LAUTALA*, H. SALOMIES, E. ELOVAARA, J. TASKINEN, (Dept. of Pharm., Div. of Pharm. Chem., P.O. Box 56, FIN-00014 Univ. of Helsinki, Helsinki, Finland)

      J. Planar Chromatogr. 9, 413-417 (1996). HPTLC of p-nitrophenol, p-nitrophenyl-b-D-glucuronide, and UDP-glucuronic acid on RP-18 with a mixture of 50 mM sodium dihydrogen phosphate, pH 2.2 and acetonitrile 3:2. Quantification by densitometry (absorbance) at 310 nm. Limit of quantification was 3 mM; repeatability of sample application determined from peak heights and peak areas was 2.2% and 2.3%, respectively; reproducibility, expressed as relative standard deviation, was 4.1-11.7%. Development and validation of a rapid and reliable HPTLC method. Also TLC of some catechol glucoronides.

      Classification: 20
      54 078
      Thin-layer chromatographic assay for endo-beta-N-acetyl-glucosaminidase activity in rat tissues
      N. COOK, J. ZANETTA, G. VINCENDON

      J. Chromatogr. 292, 479-484 (1984). HPTLC on silica with methyl acetate - chloroform - propanol - methanol - 0.25 % potassium chloride 25:20:2O:2O: 17. Quantification by in situ fluorometry at 366 nm.

      Keywords:
      Classification: 20
      78 143
      Fast and sensitive staining technique for glucose oxidase in polyacrylamide gel
      C. OBINGER*, S. PFEIFFER, W. HOFSTETTER, R. WUTKA, R. EBERMANN, (*Inst. Chem., Univ. Bodenkultur, Gregor Mendelstr. 33, 1180 Vienna, Austria)

      J. Chromatogr. A 731, 293-298 (1996). Presentation of a staining techniques for glucose oxidase activity on polyacrylamide gels, based on the fact that glucose oxidase reacts with one-electron scavengers in a reaction dependent on pH and pO2. Demonstration of reduction of ferricyanide, cuprisulfate, ferrycytochrome C and nitrotetrazolium blue reduction leading to sharp colored bands under aerobic conditions. Comparison with conventional peroxidase/O-dianisidine-assay.

      Keywords:
      Classification: 20, 32e, 36
      55 079
      Alkenylhydrolase
      J. GUNAWAN, H. DEBUCH

      J. Neurochem. 44, 370-375 (1985). Assay for microsomal alkenylhydrolyse activity of rat brain. Free aldehydes are formed in this enzymatic reaction. The analysis is based on a known TLC method for fragments of plasmalogens using silica or cellulose and chloroform - methanol - water 3:7:3. Detection with iodine vapors and/or ninhydrin, scintillation counting.

      Classification: 20
      78 188
      A rapid procedure for the purification of human salivary peroxidase
      G. MARCOZZI, (Dept. Basic & App. Biol., Univ. L'Aquila, Coppito I, Via Vetoio, 67010 L'Aquila, Italy)

      Biom. Chromatogr. 10, 97-98 (1996). Electrophoresis on 0.75 mm gels of 10% polyacrylamide. Immunodetection by using rabbit anti LPO antibodies (30mg/mL), peroxidase-anti-peroxidase soluble complex and diamino-benzidine tetrahydrochloride. Discussion of the merits of the improved procedure.

      Keywords:
      Classification: 20, 36
      55 080
      Dopamin-beta-hydroxylase
      R. SOKOLOFF, R. FRIGON, D. O'CONNOR

      J. Neurochem. 44, 411-420 (1985). The known procedure of peptide mapping after tryptic fragmentation is performed 2-dimensionally by TLC on silica with propanol -34 % NH3 7:3, followed by TLE at pH 3.5, 800 V, 50 minutes with acetic acid - pyridine - water 10:1:300. The peptides are sprayed with fluorescamine, followed by triethylamine treatment, then visualized by UV.

      Classification: 20