H-RF-OH

Ref. 3D-PP43871

Información del producto

• Nombre: H-RF-OH
• Sinónimos: NH2-Arg-Phe-OH

Descripción

Peptide H-RF-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-RF-OH include the following: Bitter-RF: a random forest machine model for recognizing bitter peptides YF Zhang, YH Wang, ZF Gu, XR Pan, J Li - Frontiers in , 2023 - frontiersin.orghttps://www.frontiersin.org/articles/10.3389/fmed.2023.1052923/full Conformational features of a synthetic cyclic peptide corresponding to the complete V3 loop of the RF HIV-1 strain in water and water/trifluoroethanol solutions WF Vranken , M Budesinsky, JC Martins - European journal of , 1996 - Wiley Online Libraryhttps://febs.onlinelibrary.wiley.com/doi/abs/10.1111/j.1432-1033.1996.00100.x Influence of charge distribution on the discrepant MS/MS fragmentation of the native and oxidized FMRF: evidence for the mobile proton model W Zong, R Liu , F Sun, P Zhang - Journal of Peptide , 2010 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.1286 Repetitive Gly-Leu-Lys-Gly-Glu-Asn-Arg-Gly-Asp peptide derived from collagen and fibronectin for improving cell-scaffold interaction P Chaisri, A Chingsungnoen , S Siri - Applied biochemistry and , 2015 - Springerhttps://link.springer.com/article/10.1007/s12010-014-1388-y CPPred-RF: a sequence-based predictor for identifying cell-penetrating peptides and their uptake efficiency L Wei , PW Xing , R Su, G Shi, ZS Ma - Journal of Proteome , 2017 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jproteome.7b00019 Glycine-directed peptide amidation: presence in rat brain of two enzymes that convert p-Glu-His-Pro-Gly-OH into p-Glu-His-Pro-NH2 (thyrotropin-releasing hormone). JS Kizer, WH Busby Jr, C Cottle - Proceedings of the , 1984 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.81.10.3228 Amyloidogenic model peptides as catalysts for stereoselective aldol reactions JNBD Pelin , BB Gerbelli , BM Soares - Catalysis Science & , 2019 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2019/cy/c9cy00790c A role for the 2' OH of peptidyl-tRNA substrate in peptide release on the ribosome revealed through RF-mediated rescue JJ Shaw , S Trobro, SL He, J aca
qvist , R Green - Chemistry & biology, 2012 - cell.comhttps://www.cell.com/ccbio/pdf/S1074-5521(12)00218-9.pdf THE CHEMICAL STRUCTURE OF THE TUBERCULIN ACTIVE PEPTIDE I. ISOLATION OF beta-ALANINE AS THE N-TERMINAL RESIDUE OF THE ACTIVE PEPTIDE I KASUYA, A HAGITANI - The Journal of Biochemistry, 1955 - jstage.jst.go.jphttps://www.jstage.jst.go.jp/article/biochemistry1922/42/6/42_6_805/_article/-char/ja/ Structure-based prediction of protein-peptide binding regions using Random Forest G Taherzadeh , Y Zhou , AWC Liew , Y Yang - Bioinformatics, 2018 - academic.oup.comhttps://academic.oup.com/bioinformatics/article-abstract/34/3/477/4237510 Rheumatoid-factor-reactive sites on CH3 established by overlapping 7-mer peptide epitope analysis C Peterson, CC Malone, RC Williams Jr - Molecular immunology, 1995 - Elsevierhttps://www.sciencedirect.com/science/article/pii/016158909400122H AIPpred: sequence-based prediction of anti-inflammatory peptides using random forest B Manavalan , TH Shin , MO Kim , G Lee - Frontiers in pharmacology, 2018 - frontiersin.orghttps://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2018.00276/full

• Marca: Biosynth