Ac-ASHLGLAR-OH
Ref. 3D-PP48042
Undefined size | To inquire |
Product Information
Peptide Ac-ASHLGLAR-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 Ac-ASHLGLAR-OH include the following: Isotope-coded N-terminal sulfonation of peptides allows quantitative proteomic analysis with increased de novo peptide sequencing capability YH Lee, H Han , SB Chang - Rapid communications in , 2004 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/rcm.1724 Protein cross-links: Universal isolation and characterization by isotopic derivatization and electrospray ionization mass spectrometry X Chen, YH Chen, VE Anderson - Analytical biochemistry, 1999 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0003269799942434 Sequence determination by MALDI-TOF mass spectrometry of an insecticidal lentil peptide of the PA1b type WG Taylor, DH Sutherland, H Zhang , DD Hegedus - Phytochemistry letters, 2015 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1874390015000531 Highly selective and large scale mass spectrometric analysis of 4-hydroxynonenal modification via fluorous derivatization and fluorous solid-phase extraction W Yuan, Y Zhang, Y Xiong, T Tao, Y Wang - Analytical , 2017 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.6b04850 Improving de novo sequencing of peptides using a charged tag and C-terminal digestion W Chen, PJ Lee, H Shion, N Ellor - Analytical chemistry, 2007 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac061670b High-throughput bioconjugation for enhanced 193 nm photodissociation via droplet phase initiated ion/ion chemistry using a front-end dual spray reactor VC Cotham , JB Shaw , JS Brodbelt - Analytical chemistry, 2015 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.5b02242 High-throughput comparative proteome analysis using a quantitative cysteinyl-peptide enrichment technology T Liu , WJ Qian , EF Strittmatter, DG Camp - Analytical , 2004 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac049485q A method for high-sensitivity peptide sequencing using postsource decay matrix-assisted laser desorption ionization mass spectrometry T Keough, RS Youngquist - Proceedings of the , 1999 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.96.13.7131 Solid-phase derivatization of tryptic peptides for rapid protein identification by matrix-assisted laser desorption/ionization mass spectrometry T Keough, MP Lacey - Rapid Communications in , 2002 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/rcm.670 Atmospheric pressure matrix-assisted laser desorption/ionization ion trap mass spectrometry of sulfonic acid derivatized tryptic peptides T Keough, MP Lacey, RJ Strife - Rapid Communications in , 2001 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/rcm.499 Dissociation mechanisms and implication for the presence of multiple conformations for peptide ions with arginine at the C-terminus: time-resolved photodissociation SH Yoon, JH Moon, MS Kim - Journal of mass spectrometry, 2010 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/jms.1773 Millisecond radiolytic modification of peptides by synchrotron X-rays identified by mass spectrometry SD Maleknia, M Brenowitz , MR Chance - Analytical chemistry, 1999 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac990500e De novo sequencing of peptides using selective 351 nm ultraviolet photodissociation mass spectrometry SA Robotham, C Kluwe, JR Cannon - Analytical , 2013 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac402309h Design and biological activity of a new generation of synthetic C3a analogues by combination of peptidic and non-peptidic elements. R Gerardy-Schahn, D Ambrosius, M Casaretto - Biochemical , 1988 - ncbi.nlm.nih.govhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1135211/ Enhancement of ultraviolet photodissociation efficiencies through attachment of aromatic chromophores L Vasicek, JS Brodbelt - Analytical chemistry, 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac102126s Induction of complement C3a receptor responses by kallikrein-related peptidase 14 K Oikonomopoulou, RA DeAngelis, H Chen - The Journal of , 2013 - journals.aai.orghttps://journals.aai.org/jimmunol/article/191/7/3858/39956 Photodissociation tandem mass spectrometry at 266 nm of an aliphatic peptide derivatized with phenyl isothiocyanate and 4-sulfophenyl isothiocyanate JY Oh, JH Moon, YH Lee, SW Hyung - Journal Devoted to , 2005 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/rcm.1922 facile fragmentation pathway of gas-phase peptide ions: a study on the gas-phase fragmentation mechanism and energetics of tryptic peptides modified with 4 JW Shin, YH Lee, S Hwang - Journal of mass , 2007 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/jms.1172 C-terminal de novo sequencing of peptides using oxazolone-based derivatization with bromine signature JS Kim , M Shin, JS Song, S An, HJ Kim - Analytical biochemistry, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0003269711005318 De novo analysis of protein N-terminal sequence utilizing MALDI signal enhancing derivatization with Br signature JS Kim , JS Song, Y Kim, SB Park , HJ Kim - Analytical and bioanalytical , 2012 - Springerhttps://link.springer.com/article/10.1007/s00216-011-5642-7 Matrix-assisted laser desorption/ionization signal enhancement of peptides by picolinamidination of amino groups JS Kim , JH Kim, HJ Kim - to the Rapid Dissemination of Up-to , 2008 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/rcm.3392 Picolinamidination of phosphopeptides for MALDI-TOF-TOF mass spectrometric sequencing with enhanced sensitivity JS Kim , E Cui, HJ Kim - Journal of the American Society for Mass , 2009 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1044030509004103 Simplifying fragmentation patterns of multiply charged peptides by N-terminal derivatization and electron transfer collision activated dissociation JA Madsen , JS Brodbelt - Analytical chemistry, 2009 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac9000942 Ultrafast ultraviolet photodissociation at 193 nm and its applicability to proteomic workflows JA Madsen , DR Boutz , JS Brodbelt - Journal of proteome research, 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/pr100515x On-tissue N-terminal peptide derivatizations for enhancing protein identification in MALDI mass spectrometric imaging strategies J Franck , M El Ayed, M Wisztorski , M Salzet - Analytical , 2009 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac901043n Collision induced decomposition of peptides. Choice of collision parameters I Haller, UA Mirza, BT Chait - Journal of the American Society for Mass , 1996 - Elsevierhttps://www.sciencedirect.com/science/article/pii/1044030596856133 Peptide sequencing using a patchwork approach and surface-induced dissociation in sector-TOF and dual quadrupole mass spectrometers FM Fernandez , LL Smith, K Kuppannan, X Yang - Journal of the American , 2003 - Springerhttps://link.springer.com/article/10.1016/j.jasms.2003.09.003 Enhanced electron transfer dissociation of peptides modified at C-terminus with fixed charges BJ Ko , JS Brodbelt - Journal of The American Society for Mass , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1007/s13361-012-0458-z Ultraviolet photodissociation of carboxylate-derivatized peptides in a quadrupole ion trap BJ Ko , JS Brodbelt - Journal of The American Society for Mass , 2011 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1007/s13361-010-0016-5
Chemical properties
Technical inquiry about: 3D-PP48042 Ac-ASHLGLAR-OH
If you want to request a quotation or place an order, please instead add the desired products to your cart and then request a quotation or order from the cart. It is faster, cheaper, and you will be able to benefit from the available discounts and other advantages.