H-YGGFLRRIR^PKLK-OH

Ref. 3D-PP49221

Produktinformation

• Name: H-YGGFLRRIR^PKLK-OH

Beschreibung

Peptide H-YGGFLRRIR^PKLK-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice. Recent citations using H-YGGFLRRIR^PKLK-OH include the following: A serine protease from suspension-cultured soybean cells ZJ Guo, C Lamb, RA Dixon - Phytochemistry, 1998 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S003194229700441X Molecular mechanism of opioid receptor selection R Schwyzer - Biochemistry, 1986 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/bi00368a075 Eukaryotic proteasomes cannot digest polyglutamine sequences and release them during degradation of polyglutamine-containing proteins P Venkatraman , R Wetzel , M Tanaka, N Nukina - Molecular cell, 2004 - cell.comhttps://www.cell.com/molecular-cell/pdf/S1097-2765(04)00151-0.pdf Rational design of peptide ligands for the kappa opioid receptor MJ Przydzial - 2005 - search.proquest.comhttps://search.proquest.com/openview/69d929b4fdb3bcc3338b3381625a128b/1?pq-origsite=gscholar&cbl=18750&diss=y Enzymatic properties of venoms from Brazilian scorpions of Tityus genus and the neutralisation potential of therapeutical antivenoms EJ Venancio , FCV Portaro , AK Kuniyoshi, DC Carvalho - Toxicon, 2013 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0041010113000822 Side Chain Cleavage in TEMPO-assisted Free Radical Initiated Peptide Sequencing (FRIPS): Amino Acid Composition Information# CS Lee, I Jang, S Hwangbo, B Moon - Bulletin of the Korean , 2015 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/bkcs.10150 Identification of a plant aminopeptidase with preference for aromatic amino acid residues as a novel member of the prolyl oligopeptidase family of serine proteases A Tsuji, Y Fujisawa, T Mino - The journal of , 2011 - academic.oup.comhttps://academic.oup.com/jb/article-abstract/150/5/525/827169 High-Throughput Synthesis of Peptide alpha-Thioesters: A Safety Catch Linker Approach Enabling Parallel Hydrogen Fluoride Cleavage A Brust , CI Schroeder , PF Alewood - ChemMedChem, 2014 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cmdc.201300524

• Marke: Biosynth