ence of CSTX-1 from the multicomponent venom of Cupiennius salei (araneae: ctenidae). Toxicon, 1994, 32, 287-302. 2J. Schaller, U. Kmpfer, S. Schrch, L. Kuhn- Nentwig, S. Haeberli, W. Nentwig, CSTX-9, a toxic peptide from the spider Cupiennius salei: amino acid sequence, disulfide bridge pattern and comparison with other spider toxins containing the cystine knot structure. Cell Mol. Life Sci., 2001, 58, 1538-1545. 3J. Schaller, L. Kuhn-Nentwig, S. Schrch, U. Kmpfer, J. Mller, W. Nentwig, Neurotoxic peptides in the multicomponent venom of the spider Cupiennius salei. Part I. Primary structure of neurotoxic peptides in relation to their biological function. Chimia 2001, 55, 1058-1062. 4S. Schrch, J. Schaller, U. Kmpfer, L. Kuhn- Nentwig, W. Nentwig, Neurotoxic peptides in the multicomponent venom of the spider Cupiennius salei. Part II. Elucidation of the disulfide-bridge pattern of the neurotoxic peptide CSTX-9 by tandem mass spectrometry. Chimia 2001, 55, 1063-1066.
Authors
Stefan Schrch1, Johann Schaller 1, Urs Kmpfer 1, Lucia Kuhn-Nentwig2, Stefan Knig3 1Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland 2Zoological Institute, University of Bern, Baltzerstrasse 6, CH-3012 Bern, Switzerland 3Applied Biosystems, Grundstrasse 10, 6343 Rotkreuz, Switzerland
'"/>Source:
Page: All 1 2 3 4 5 Related biology technology :1.
Efficiently Insert Unique Restriction Sites into Plasmid Vectors2.
Efficient Cleavage of Fusion Proteins to Yield Native Amino Termini3.
Mammalian Expression Vector for Efficient Cloning of PCR Fragments4.
Efficient Transfection of Neurospora Crassa5.
Efficient Transfection of Neurospora Crassa6.
Efficient Recovery of Ultrapure Plasmid DNA7.
Efficient and Reliable PCR Setup Using Eppendorf MasterMix8.
Efficient DNA transfection of primary CNS neurons using TransMessenger
Transfection Reagent9.
Efficient RNAi-mediated gene silencing in neuronal cells using QIAGEN
siRNA and TransMessenger Transfection Reagent*10.
Cloning Based on Efficient Three-Fragment Assembly
DNA Ligation11.
Efficient and Reliable Linear
Amplification of cRNA