Das Produkt wurde korrekt in den Warenkorb gelegt.

discount label
H-AA-OH
3D-Ansicht

Biosynth logo

H-AA-OH

Ref. 3D-PP43679

1mg
172,00 €
10mg
196,00 €
100mg
303,00 €
Voraussichtliche Lieferung in Vereinigte Staaten, am Freitag 27. Dezember 2024

Produktinformation

Name:
H-AA-OH
Synonyme:
  • NH2-Ala-Ala-OH
Beschreibung:

Peptide H-AA-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-AA-OH include the following: Mutational analysis of designed peptides that undergo structural transition from alpha helix to beta sheet and amyloid fibril formation Y Takahashi, A Ueno, H Mihara - Structure, 2000 - cell.comhttps://www.cell.com/structure/pdf/S0969-2126(00)00183-0.pdf Structure-activity relationship of HP (2-20) analog peptide: Enhanced antimicrobial activity by N-terminal random coil region deletion Y Park, SC Park, HK Park, SY Shin - Peptide Science , 2007 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/bip.20679 New selectivity and turnover in peptide hydrolysis by metal complexes. A palladium (II) aqua complex catalyzes cleavage of peptides next to the histidine residue TN Parac , NM Kostic - Journal of the American Chemical Society, 1996 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja952162e Messenger RNA-programmed incorporation of multiple N-methyl-amino acids into linear and cyclic peptides T Kawakami, H Murakami , H Suga - Chemistry & biology, 2008 - cell.comhttps://www.cell.com/trends/molecular-medicine/fulltext/S1074-5521(07)00447-4 Amino acid and peptide dynamics in horticultural soils under conventional and organic management strategies T Ge , H Yuan, P Roberts , DL Jones , H Qin - Journal of soils and , 2012 - Springerhttps://link.springer.com/article/10.1007/s11368-011-0457-x Peptide framework for screening the effects of amino acids on assembly S Hamsici , AD White , H Acar - Science Advances, 2022 - science.orghttps://www.science.org/doi/abs/10.1126/sciadv.abj0305 Environmental photochemistry of amino acids, peptides and proteins RA Lundeen , EML Janssen , C Chu , K McNeill - Chimia, 2014 - chimia.chhttps://www.chimia.ch/chimia/article/view/5661 Studies of synthetic peptide analogs of the amphipathic helix. Effect of charged amino acid residue topography on lipid affinity. P Kanellis, AY Romans, BJ Johnson, H Kercret - Journal of Biological , 1980 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0021925819703147 Slow peptide bond formation by proline and other N-alkylamino acids in translation MY Pavlov, RE Watts, Z Tan - Proceedings of the , 2009 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.0809211106 Salt induced peptide formation: on the selectivity of the copper induced peptide formation under possible prebiotic conditions MG Schwendinger, R Tattler, S Saetia, KR Liedl - Inorganica chimica , 1995 - Elsevierhttps://www.sciencedirect.com/science/article/pii/002016939404186Y The hydrophobic core sequence modulates the neurotoxic and secondary structure properties of the prion peptide 106-126 MF Jobling, LR Stewart, AR White - Journal of , 1999 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1046/j.1471-4159.1999.0731557.x New chemical descriptors relevant for the design of biologically active peptides. A multivariate characterization of 87 amino acids M Sandberg, L Eriksson, J Jonsson - Journal of medicinal , 1998 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm9700575 Rapid"tea-bag" peptide synthesis using 9-fluorenylmethoxycarbonyl (Fmoc) protected amino acids applied for antigenic mapping of viral proteins M Sallberg, U Ruden, LO Magnius, E Norrby - Immunology letters, 1991 - Elsevierhttps://www.sciencedirect.com/science/article/pii/016524789190090W Endogenous peptides with distinct amino acid anchor residue motifs bind to HLA-A1 and HLA-B8. M DiBrino, KC Parker, J Shiloach - (Baltimore, Md.: 1950 , 1994 - journals.aai.orghttps://journals.aai.org/jimmunol/article-abstract/152/2/620/27215 Enzyme modification by MPEG with an amino acid or peptide as spacer arms L Sartore , P Caliceti, O Schiavon - Applied biochemistry and , 1991 - Springerhttps://link.springer.com/article/10.1007/BF02921514 Inefficient Delivery but Fast Peptide Bond Formation of Unnatural l-Aminoacyl-tRNAs in Translation KW Ieong , MY Pavlov, M Kwiatkowski - Journal of the , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja3063524 Peptide bond synthesis catalyzed by subtilisin, papain, and pepsin K Morihara, T Oka - The Journal of Biochemistry, 1981 - academic.oup.comhttps://academic.oup.com/jb/article-abstract/89/2/385/2186522 Ionic liquids: new targets and media for alpha-amino acid and peptide chemistry JC Plaquevent, J Levillain , F Guillen, C Malhiac - Chemical , 2008 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/cr068218c A general method for designing combinatorial peptide libraries decodable by amino acid analysis J Kofoed, JL Reymond - Journal of combinatorial chemistry, 2007 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/cc7001155 Montmorillonite catalyzed peptide bond formation: The effect of exchangeable cations J Bujdak , H Le Son, BM Rode - Journal of inorganic biochemistry, 1996 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0162013495001867 Peptide bond formation on the surface of activated alumina: peptide chain elongation J Bujdak , BM Rode - Catalysis letters, 2003 - Springerhttps://link.springer.com/article/10.1023/B:CATL.0000007148.33571.f7 Characterization of bioactive RGD peptide immobilized onto poly (acrylic acid) thin films by plasma polymerization HS Seo, YM Ko, JW Shim, YK Lim, JK Kook - Applied Surface , 2010 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0169433210009827 High performance liquid chromatographic study of the retention and separation of short chain peptide diastereomers on a C8 bonded phase EP Kroeff, DJ Pietrzyk - Analytical Chemistry, 1978 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ac50031a040 Ribosomal Synthesis of Macrocyclic Peptides with Linear γ4- and beta-Hydroxy-γ4-amino Acids E Adaligil , A Song, CN Cunningham - ACS chemical , 2021 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acschembio.1c00292 Use of a peptide rather than free amino acid nitrogen source in chemically defined"elemental" diets DBA Silk, PD Fairclough, ML Clark - Journal of Parenteral , 1980 - Wiley Online Libraryhttps://aspenjournals.onlinelibrary.wiley.com/doi/abs/10.1177/0148607180004006548 Hydrolysis of N-terminal peptide bonds and amino acid derivatives by the beta-hydroxoaquotriethylenetetraminecobalt (III) ion DA Buckingham, JP Collman - Journal of the , 1967 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ja00981a008 Free and peptide amino acid net flux across the rumen and the mesenteric-and portal-drained viscera of sheep D Remond, L Bernard, C Poncet - Journal of animal science, 2000 - academic.oup.comhttps://academic.oup.com/jas/article-abstract/78/7/1960/4625824 Spontaneous peptide bond cleavage in aging alpha-crystallin through a succinimide intermediate. CE Voorter, WA de Haard-Hoekman - Journal of Biological , 1988 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0021925818373836 BG de la Torre , F Albericio - Molecules, 2020 - mdpi.comhttps://www.mdpi.com/1420-3049/25/10/2293

Hinweis:
Unsere Produkte sind nur für Laborzwecke. Für jede andere Verwendung, bitte melden sie sich bei uns.
Marke:
Biosynth
Langzeitlagerung:
Hinweise:

Chemische Eigenschaften

MDL:
Schmelzpunkt:
Siedepunkt:
Flammpunkt:
Dichte:
Konzentration:
EINECS:
Merck:
HS-Code:

Gefahrenhinweise

UN-Nummer:
EQ:
Klasse:
H-Sätze:
P-Sätze:
Flugverbot:
Gefahrenhinweis:
Verpackungsgruppe:
LQ:

Technische Anfrage zu: 3D-PP43679 H-AA-OH

Bitte verwenden Sie stattdessen den Warenkorb, um ein Angebot oder eine Bestellung anzufordern

Wenn Sie ein Angebot anfordern oder eine Bestellung aufgeben möchten, legen Sie stattdessen die gewünschten Produkte in Ihren Warenkorb und fordern Sie dann ein Angebot oder eine Bestellung an aus dem Warenkorb. Es ist schneller, billiger und Sie können von den verfügbaren Rabatten und anderen Vorteilen profitieren.

* Obligatorische felder
Willkommen bei CymitQuimica!Wir verwenden Cookies, um Ihren Besuch zu verbessern. Wir schließen Werbung nicht ein.

Bitte beachten Sie unsere Cookie-Richtlinie  für weitere Details oder passen Sie Ihre Einstellungen unter “Konfigurieren” an.