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. Chromatogr. 698, 225-250 (1995). A review with 237 references on the indications and limitations of high-resolution two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) as an aid in the analysis of the clonality of immunoglobulins with regard to „standard“ techniques such as immunofixation electrophoresis. Discussion of the use of the technique in laboratories experienced in defining monoclonal gammopathy both for diagnostic and for research purposes.
J. Chromatogr. B 668, 1-11 (1995). Identification of two proteins, which are bound to Jacalin, by SDS-PAGE. Discussion of the retention and some features of the proteins. It was shown that Jacalin also binds several proteolytic enzymes which remain to be identified.
Anal. Biochem. 239, 123-129 (1996). Two-dimensional electrophoresis on polyacrylamide gel (PAG) with 0.025 M Tris-0.195 M glycine buffer (pH 8.6) at a constant 30 mA electric current. Fixation with 1% acetic acid, and staining with o-dianisidine solution. Discussion of Hb binding with some of the smaller individual polymeric molecules of Hp subtypes and variants. Detection also of the capacity for combining with hemoglobin of each polymer of the variants.
J. Chromatogr. 13, 756 (1/2), 141-150 (2001). Presentation of an overview of methods combining basic procedures in glycochemistry with various applications of electrophoresis that allow investigating single allergens in crude extracts. Analysis of various allergen extracts, e.g. from tomato, grass pollen and bacteria.
J. Chromatogr. 698, 181-201 (1995). A review with 92 references on fluorogenic substrates to detect hydrolytic enzymes after electrophoretic separations. Discussion of the factors affecting sensitivity and specificity of the title substrates, with some examples, and of the application to clinical, biological and food chemistry.
J. Chromatogr. 698, 145-162 (1995). A review with 99 references on the methods for the electrophoretic recovery of proteins from polyacrylamide gel, including principles, advantages and disadvantages, and updated information on related techniques.
J. Chinese Pharm. Univ. (Zhongguo Yaoke Daxue Xuebao) 27, 159-162 (1996). Presentation of a new method based on a silica plate coupling electrophoresis and chromatography in one step development to give a bidimensional chromato-electrophoresis map. Description of the device in which a parallel electric field can be put upon the plate in vertical direction. Investigation of the relationship between horizontal migration and electric field strength.
J. Chromatogr. A, 921 (1), 57-67 (2001). Characterization of clotting factor IX preparations from human plasma (pdFIX) using electrophoretic methods like SDS-PAGE, isoelectric focusing and 2-D PAGE. Separation of factor IX prior to and after activation with factor XIa by 1-D and 2-D PAGE and on isoelectric focusing gels. Identification of vitronectin by immunological techniques as major accompanying plasma protein, separated from Factor IX and characterized by isoelectric focusing and 2D-PAGE.