Le produit a bien été ajouté au panier.

discount label
5TAMRA-R-OH
Vue en 3D

Biosynth logo

5TAMRA-R-OH

Ref. 3D-PP44499

Taille indéfinieÀ demander
Livraison estimée en/au États-Unis, le mardi 3 décembre 2024

Informations sur le produit

Nom :
5TAMRA-R-OH
Synonymes :
  • 5Thr-Ala-Met-Arg-Ala-Arg-OH
Description :

Peptide 5TAMRA-R-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 5TAMRA-R-OH include the following: Quantitative structure-activity relationship study of antioxidative peptide by using different sets of amino acids descriptors YW Li , B Li, J He, P Qian - Journal of Molecular Structure, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S002228601100384X Conjugation of a photosensitizer to an oligoarginine-based cell-penetrating peptide increases the efficacy of photodynamic therapy Y Choi , JR McCarthy, R Weissleder - ChemMedChem , 2006 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cmdc.200500036 Role of peptide hydrophobicity in the mechanism of action of alpha-helical antimicrobial peptides Y Chen , MT Guarnieri , AI Vasil, ML Vasil - Antimicrobial agents , 2007 - Am Soc Microbiolhttps://journals.asm.org/doi/abs/10.1128/aac.00925-06 Peptide modifications differentially alter G protein-coupled receptor internalization and signaling bias V Made, S Babilon, N Jolly, L Wanka - Angewandte Chemie , 2014 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201403750 Systemic in vivo distribution of activatable cell penetrating peptides is superior to that of cell penetrating peptides TA Aguilera , ES Olson, MM Timmers, T Jiang - Integrative , 2009 - academic.oup.comhttps://academic.oup.com/ib/article-abstract/1/5-6/371/5211408 C-end rule peptides mediate neuropilin-1-dependent cell, vascular, and tissue penetration T Teesalu , KN Sugahara - Proceedings of the , 2009 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.0908201106 Concomitant Occurrence of Peptide 310- and alpha-Helices Probed by NMR S Mammi, M Rainaldi, M Bellanda - Journal of the , 2000 - ACS Publicationshttps://pubs.acs.org/doi/full/10.1021/ja002710a Stearylated arginine-rich peptides: a new class of transfection systems S Futaki, W Ohashi, T Suzuki, M Niwa - Bioconjugate , 2001 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bc015508l Arginine-rich peptides: an abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery S Futaki, T Suzuki, W Ohashi, T Yagami - Journal of Biological , 2001 - ASBMBhttps://www.jbc.org/article/S0021-9258(19)46333-3/abstract Translocation of branched-chain arginine peptides through cell membranes: flexibility in the spatial disposition of positive charges in membrane-permeable peptides S Futaki, I Nakase, T Suzuki, Zhang , Y Sugiura - Biochemistry, 2002 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi0256173 Cell-surface interactions on arginine-rich cell-penetrating peptides allow for multiplex modes of internalization S Futaki, I Nakase - Accounts of chemical research, 2017 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.accounts.7b00221 Arginine-rich peptides: potential for intracellular delivery of macromolecules and the mystery of the translocation mechanisms S Futaki - International journal of pharmaceutics, 2002 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S037851730200337X Arginine-rich cell penetrating peptides: Design, structure-activity, and applications to alter pre-mRNA splicing by steric-block oligonucleotides R Abes, A Arzumanov, H Moulton - European Peptide , 2008 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.979 Exploring the sequence space for (tri-) peptide self-assembly to design and discover new hydrogels PWJM Frederix , GG Scott, YM Abul-Haija - Nature , 2015 - nature.comhttps://www.nature.com/articles/nchem.2122 Design, synthesis, and evaluation of amphiphilic cyclic and linear peptides composed of hydrophobic and positively-charged amino acids as antibacterial agents N Riahifard, S Mozaffari , T Aldakhil, F Nunez - Molecules, 2018 - mdpi.comhttps://www.mdpi.com/1420-3049/23/10/2722 Selective amino acid substitution reduces cytotoxicity of the antimicrobial peptide mastoparan LN Irazazabal, WF Porto , SM Ribeiro , S Casale - et Biophysica Acta (BBA , 2016 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0005273616302449 Synthesis and application of unprotected cyclic peptides as building blocks for peptide dendrimers L Zhang, JP Tam - Journal of the American Chemical Society, 1997 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja9621105 Molecular transporters for peptides: delivery of a cardioprotective ϵPKC agonist peptide into cells and intact ischemic heart using a transport system, R7 L Chen, LR Wright, CH Chen, SF Oliver, PA Wender - Chemistry & biology, 2001 - cell.comhttps://www.cell.com/ccbio/pdf/S1074-5521(01)00076-X.pdf Antibacterial activities of ferrocenoyl-and cobaltocenium-peptide bioconjugates JT Chantson, MVV Falzacappa, S Crovella - Journal of , 2005 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0022328X05005243 Effects of cargo molecules on the cellular uptake of arginine-rich cell-penetrating peptides JR Maiolo, M Ferrer , EA Ottinger - Biochimica et Biophysica Acta (BBAhttps://www.sciencedirect.com/science/article/pii/S0005273605001094 Peptide synthesis using unprotected peptides through orthogonal coupling methods. JP Tam , YIAN Lu, CFA Liu - Proceedings of the , 1995 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.92.26.12485 ω-Amino acids in peptide design. Crystal structures and solution conformations of peptide helices containing a beta-alanyl-γ-aminobutyryl segment IL Karle, A Pramanik , A Banerjee - Journal of the , 1997 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja970566w A helix-stabilized cell-penetrating peptide as an intracellular delivery tool H Yamashita, M Oba , T Misawa, M Tanaka - , 2016 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.201500468 Sequence-specific Ni (II)-dependent peptide bond hydrolysis for protein engineering: reaction conditions and molecular mechanism E Kopera, A Krezel , AM Protas, A Belczyk - Inorganic , 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ic1005709 Neuroprotective peptides fused to arginine-rich cell penetrating peptides: Neuroprotective mechanism likely mediated by peptide endocytic properties BP Meloni , D Milani, AB Edwards , RS Anderton - Pharmacology & , 2015 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0163725815001175 Selective peptide bond hydrolysis of cysteine peptides in the presence of Ni (II) ions AM Protas, A Bonna , E Kopera, W Bal - Journal of inorganic biochemistry, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0162013410002175 Prediction of peptide retention at different HPLC conditions from multiple linear regression models , M Marszaà ‚à ‚ , YV Heyden , R Kaliszan - Journal of Proteome , 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/pr049780r

Avis:
Nos produits sont destinés uniquement à un usage en laboratoire. Pour tout autre usage, veuillez nous contacter.
Marque:
Biosynth
Stockage à long terme :
Notes :

Propriétés chimiques

MDL:
Point de fusion :
Point d'ébullition :
Point d'éclair :
Densité :
Concentration :
EINECS :
Merck :
Code SH :

Informations sur les risques

Numéro ONU :
EQ:
Classe :
Phrases R :
Phrases S :
Transport aérien interdit :
Informations sur les risques :
Groupe d'emballage :
LQ :

Question d’ordre technique sur : 3D-PP44499 5TAMRA-R-OH

Veuillez plutôt utiliser le panier afin de demander un devis ou passer commande

Si vous souhaitez demander un devis ou passer commande, veuillez plutôt ajouter les produits souhaités à votre panier, puis demander un devis ou passer commande à partir de votre panier. C'est une méthode plus rapide, plus économique, et vous pourrez bénéficier des remises disponibles ainsi que d'autres avantages

* Champ obligatoire
Bienvenue chez CymitQuimica !Nous utilisons des cookies pour améliorer votre visite. Nous n’incluons pas de publicité.

Veuillez consulter notre Politique de Cookies pour plus de détails ou ajustez vos préférences dans "Configurer".