H-SAPDTRPAP-OH
Ref. 3D-PP46411
1mg | 217,00 € | ||
10mg | 253,00 € | ||
100mg | 455,00 € |
Produktinformation
- NH2-Ser-Ala-Pro-Asp-Thr-Arg-Pro-Ala-Pro-OH
Peptide H-SAPDTRPAP-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-SAPDTRPAP-OH include the following: Humoral immunity against a tandem repeat epitope of human mucin MUC-1 in sera from breast, pancreatic, and colon cancer patients Y Kotera, JD Fontenot, G Pecher, RS Metzgar, OJ Finn - Cancer research, 1994 - AACRhttps://aacrjournals.org/cancerres/article-abstract/54/11/2856/499996 Epitope mapping of anti-breast and anti-ovarian mucin monoclonal antibodies X Pei-Xiang, J Prenzoska, IFC McKenzie - Molecular immunology, 1992 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0161589092902018 T cells recognize PD (N/T) R motif common in a variable number of tandem repeat and degenerate repeat sequences of MUC1 VM Pisarev , L Kinarsky, T Caffrey , FG Hanisch - International , 2005 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1567576904003224 The use of fluoroproline in MUC1 antigen enables efficient detection of antibodies in patients with prostate cancer VJ Somovilla , IA Bermejo, IS Albuquerque - Journal of the , 2017 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jacs.7b09447 A synthetic MUC1 glycopeptide bearing betaGalNAc-Thr as a Tn antigen isomer induces the production of antibodies against tumor cells V Leiria Campo , TB Riul, L Oliveira Bortot - , 2017 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.201600473 Immune recognition of tumor-associated mucin MUC1 is achieved by a fully synthetic aberrantly glycosylated MUC1 tripartite vaccine V Lakshminarayanan, P Thompson - Proceedings of the , 2012 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.1115166109 MUC1 vaccines, comprised of glycosylated or non-glycosylated peptides or tumor-derived MUC1, can circumvent immunoediting to control tumor growth in MUC1 V Lakshminarayanan, NT Supekar , J Wei, DB McCurry - PloS one, 2016 - journals.plos.orghttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0145920 Glycosylated (Tn) and Anchor-Modified MUC1 Peptide Vaccines Induce Effective Anti tumor Immunity and Break Tolerance in MUC1 Transgenic Mice V Lakshminarayanan, JM Bradley, LB Pathangey - Cancer Research, 2010 - AACRhttps://aacrjournals.org/cancerres/article/70/8_Supplement/2403/562854 Immunotherapy with glycosylated and anchor-modified MUC1 peptides breaks tolerance in MUC1 transgenic mice V Lakshminarayanan, J Bradley, T Tinder, L Pathangey - Cancer Research, 2008 - AACRhttps://aacrjournals.org/cancerres/article-abstract/68/9_Supplement/2860/548576 Induction of HLA-A2-restricted CTLs to the mucin 1 human breast cancer antigen. V Apostolopoulos , V Karanikas, JS Haurum - (Baltimore, Md.: 1950 , 1997 - journals.aai.orghttps://journals.aai.org/jimmunol/article-abstract/159/11/5211/30949 Peptide mimics of a tumor antigen induce functional cytotoxic T cells V Apostolopoulos , SA Lofthouse, V Popovski - Nature , 1998 - nature.comhttps://www.nature.com/articles/nbt0398-276 MUC1 peptide epitopes associated with five different H-2 class I molecules V Apostolopoulos , JS Haurum - European journal of , 1997 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/eji.1830271017 Getting into the groove: unusual features of peptide binding to MHC class I molecules and implications in vaccine design V Apostolopoulos , IF McKenzie, IA Wilson - Front Biosci, 2001 - article.imrpress.comhttps://article.imrpress.com/bri/Landmark/articles/pdf/LandmarkA683.pdf Vaccine Development Against Novel Breast Cancer Antigens V Apostolopoulos , I McKenzie - 2002 - apps.dtic.milhttps://apps.dtic.mil/sti/citations/tr/ADA409560 Anti-MUC1 antibodies react directly with MUC1 peptides presented by class I H2 and HLA molecules V Apostolopoulos , G Chelvanayagam - The Journal of , 1998 - journals.aai.orghttps://journals.aai.org/jimmunol/article/161/2/767/31120 Noncanonical peptides in complex with MHC class I V Apostolopoulos , E Lazoura - Expert Review of Vaccines, 2004 - Taylor & Francishttps://www.tandfonline.com/doi/abs/10.1586/14760584.3.2.151 MUC1-specific Cytotoxic T Lymphocytes Eradicate Tumors When Adoptively Transferred in Vivo P Mukherjee , AR Ginardi, TL Tinder, CJ Sterner - Clinical cancer , 2001 - AACRhttps://aacrjournals.org/clincancerres/article-abstract/7/3/848s/200197 Comparative immunogenicity of a cytotoxic T cell epitope delivered by penetratin and TAT cell penetrating peptides N Brooks, S Esparon, D Pouniotis, GA Pietersz - Molecules, 2015 - mdpi.comhttps://www.mdpi.com/1420-3049/20/8/14033 Immunogenicity of a tripartite cell penetrating peptide containing a MUC1 variable number of tandem repeat (VNTR) and AT helper epitope N Brooks, J Hsu, S Esparon, D Pouniotis, GA Pietersz - Molecules, 2018 - mdpi.comhttps://www.mdpi.com/1420-3049/23/9/2233 Selection and characterization of MUC1-specific CD8+ T cells from MUC1 transgenic mice immunized with dendritic-carcinoma fusion cells J Gong, V Apostolopoulos , D Chen, H Chen - , 2000 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1046/j.1365-2567.2000.00101.x Definition of MHC-restricted CTL epitopes from non-variable number of tandem repeat sequence of MUC1 GA Pietersz, W Li, C Osinski, V Apostolopoulos - Vaccine, 2000 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0264410X99005150 Design of a MUC1-based cancer vaccine FG Hanisch - 2005 - portlandpress.comhttps://portlandpress.com/biochemsoctrans/article-abstract/33/4/705/65160 Rapid induction of primary human CD4+ and CD8+ T cell responses against cancer-associated MUC1 peptide epitopes. B Agrawal, MJ Krantz, MA Reddish - International , 1998 - academic.oup.comhttps://academic.oup.com/intimm/article-abstract/10/12/1907/744541
Chemische Eigenschaften
Technische Anfrage zu: 3D-PP46411 H-SAPDTRPAP-OH
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.