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. of Medicinal Chemistry 32, 297-301 (1989). TLC of N- (dipeptidyl)-S-acetylcysteamine and N, N’- (dipeptyl)cystamine on silica. Detection under UV, exposure to iodine vapor or spraying with ninhydrin.
Acta Chimica, 127, 569-579 (1990). TLC of the chemotactic peptides on silica with chloroform - methanol 1:9, butanol - acetic acid - water 4:1:1, pyridine - acetic acid - water - ethyl acetate 20:6:11:333 or 20:6:11:56. Detection by spraying with ninhydrin, chlorine-o-tolidine or Pauly’s reagent.
Anal. Biochem. 237, 24-29 (1996). Separation with different sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Clear resolution by addition of 8 M urea to the gel and use of a multiphasic buffer system employing bicine and sulfate as trailing and leading ions, respectively. Discussion of the migration of the peptides. Demonstration of the usefulness of the system for the analysis of the title compounds generated during cellular metabolism by immunolabeled peptides secreted by cell transfected with a myloid precursor protein CDOAS.
Acta Chimica 120, 23-28 (1985). TLC study of chemically reactive synthetic derivatives of peptide hormones and hormone fragments. TLC on silica with ethyl acetate - pyridine - acetic acid - water 240:20:6:11 (S1), ethyl acetate - pyridine - acetic acid - water 120:20:6:11 (S2), ethyl acetate - pyridine - acetic acid - water 60:20:6:11 (S3), ethyl acetate - methanol 5:1 (S4), butanol - acetic acid - water 4:1:1 (S5), ethyl acetate - pyridine - acetic acid - water 30:20:6:11 (S6). Boc-lys(Z)-tyr-gly-gly-phe-leu-OMe (S1), boc-lys-tyr-gly-gly-phe-leu-OMe (S3), boc-lys(Q)-tyr-gly-gly-phe-leu-OMe (S4 and S2), H-lys(Q)-tyr-gly-gly-phe-leu-OMe.HCl (S2 and S4), H-lys-tyr-gly-gly-phe-leu-OMe.2 CH3COOH (S6), Q-tyr-gly-gly-phe-leu-OH (S2 and S5). Detection visual and under UV 254 nm.
J. of Medicinal Chemistry 31, 742-744 (1988). TLC of (Mpr1,D-phe2, Val4)arginine-vasopressin and (DesCys1,D-Phe2,Val4,DL-Aad6)arginine-vasopressin on silica with 1-butanol - pyridine - acetic acid - water 15:10:3:12; TLC of (Pmp1,D-Phe2, Val4)arginine-vasopresin with 1-butanol - ethyl acetate - acetic acid - water 1:1:1:1. Visualization with 10% Clorox-1% potassium iodide-starch.
J. of Medicinal Chemistry 32, 698-703 (1989). TLC of opioid peptide analogues on silica with butanol - pyridine - acetone - water 15:10:3:12. Detection under UV 254 nm.
J. Liquid Chromatogr. 13, 2757-2769 (1990). TLC of microwave-induced acid hydrolysis products of peptides on silica with phenol - water - aqueous 0.4% trifluoroacetic acid 150:50:5. Visualization by spraying with ninhydrin reagent. Elucidation of the hydrolysis mechanisms by TLC and TLC/MS.
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.