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R-S-R
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R-S-R

Ref. 3D-PP44614

Tamaño no definidoA consultar
Entrega estimada en Estados Unidos, el Martes 3 de Diciembre de 2024

Información del producto

Nombre:
R-S-R
Sinónimos:
  • H-RSR-OH
Descripción:

Peptide R-S-R 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 R-S-R include the following: Modular structure of genes encoding multifunctional peptide synthetases required for non-ribosomal peptide synthesis T Stachelhaus, MA Marahiel - FEMS microbiology letters, 1995 - academic.oup.comhttps://academic.oup.com/femsle/article-abstract/125/1/3/506502 The YSIRK-G/S motif of staphylococcal protein A and its role in efficiency of signal peptide processing T Bae, O Schneewind - Journal of bacteriology, 2003 - Am Soc Microbiolhttps://journals.asm.org/doi/abs/10.1128/jb.185.9.2910-2919.2003 Fast events in protein folding: helix melting and formation in a small peptide S Williams, TP Causgrove , R Gilmanshin, KS Fang - Biochemistry, 1996 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi952217p SapT, a lanthionine-containing peptide involved in aerial hyphae formation in the streptomycetes S Kodani, MA Lodato , MC Durrant - Molecular , 2005 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-2958.2005.04921.x The pH-rate profile for the hydrolysis of a peptide bond RM Smith, DE Hansen - Journal of the American Chemical , 1998 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja9804565 Recognition of a high-affinity phosphotyrosyl peptide by the Src homology-2 domain of p56lck MJ Eck, SE Shoelson , SC Harrison - Nature, 1993 - nature.comhttps://www.nature.com/articles/362087a0 Highly efficient and chemoselective peptide ubiquitylation KS Ajish Kumar, M Haj-Yahya - (International ed. in , 2009 - infoscience.epfl.chhttps://infoscience.epfl.ch/record/142089/files/8090_ftp.pdf A synthetic peptide ligase K Severin , DH Lee , AJ Kennan, MR Ghadiri - Nature, 1997 - nature.comhttps://www.nature.com/articles/39556 Stabilization of the ribonuclease S-peptide alpha-helix by trifluoroethanol JW Nelson, NR Kallenbach - Proteins: Structure, Function, and , 1986 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/prot.340010303 Ribonuclease S-peptide as a carrier in fusion proteins JS Kim , RT Raines - Protein Science, 1993 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/pro.5560020307 Thermodynamics of the binding of S-peptide to S-protein to form ribonuclease S' JM Sturtevant, RP Hearn, FM Richards, GD Watt - Biochemistry, 1971 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/bi00781a013 An experimental procedure for increasing the structural resolution of chemical hydrogen-exchange measurements on proteins: application to ribonuclease S peptide JJ Rosa, FM Richards - Journal of molecular biology, 1979 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0022283679904005 Enzymic resynthesis of the hydrolyzed peptide bond (s) in ribonuclease S GA Homandberg, M Laskowski - Biochemistry, 1979 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/bi00571a006 Barriers to rotation of secondary amide peptide bonds G Scherer, ML Kramer, M Schutkowski - Journal of the , 1998 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja980181t Structure-activity relationships of de novo designed cyclic antimicrobial peptides based on gramicidin S DL Lee, RS Hodges - Peptide Science, 2003 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/bip.10374 of single d-amino acid substitutions on disruption of beta-sheet structure and hydrophobicity in cyclic 14-residue antimicrobial peptide analogs related to gramicidin S DL Lee, JPS Powers, K Pflegerl - Journal of peptide , 2004 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1046/j.1399-3011.2003.00106.x A self-replicating peptide DH Lee , JR Granja , JA Martinez, K Severin , MR Ghadiri - Nature, 1996 - nature.comhttps://www.nature.com/articles/382525a0 An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides CE Schafmeister , J Po, GL Verdine - Journal of the American , 2000 - ACS Publicationshttps://pubs.acs.org/doi/full/10.1021/ja000563a A possible primordial peptide cycle C Huber, W Eisenreich, S Hecht, G Wachtershauser - Science, 2003 - science.orghttps://www.science.org/doi/abs/10.1126/science.1086501 Slow release of molecules in self-assembling peptide nanofiber scaffold , LD Unsworth , S Koutsopoulos, S Zhang - Journal of controlled , 2006 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0168365906003270

Aviso:
Nuestros productos están destinados únicamente para uso en laboratorio. Para cualquier otro uso, por favor contáctenos.
Marca:
Biosynth
Almacenamiento de larga duración:
Notas:

Propiedades químicas

Peso molecular:
417.5 g/mol
Fórmula:
C15H31N9O5
MDL:
Punto de fusión:
Punto de ebullición:
Punto de inflamabilidad:
Densidad:
Concentración:
EINECS:
Merck:
Código HS:

Información de peligrosidad

Número UN:
Cantidad exceptuada (EQ):
Clase:
Frases H:
Frases P:
Prohibido volar:
Información de peligrosidad:
Grupo de empaquetado:
Cantidad limitada (LQ):

Consulta técnica sobre: 3D-PP44614 R-S-R

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