Peptides

Peptide H-SSYSYSSL-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-SSYSYSSL-OH include the following: Positive selection of thymocytes PJ Fink, MJ Bevan - Advances in immunology, 1995 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0065277608606306 Positive and Negative Selection Invoke Distinct Signaling Pathways MJ Bevan, RM Perlmutter - ncbi.nlm.nih.govhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192689/ Outer membrane vesicles from the gut microbiome contribute to tumor immunity by eliciting cross-reactive T cells M Tomasi , E Caproni, M Benedet, I Zanella - Frontiers in , 2022 - frontiersin.orghttps://www.frontiersin.org/articles/10.3389/fonc.2022.912639/full Outer Membrane Vesicles From The Gut Microbiome Contribute to Tumor Immunity by Eliciting Cross-Reactive T Cells M Bellone , Q Kong, AG Goubet, U Genacašve, G Grandi - academia.eduhttps://www.academia.edu/download/107857478/pdf.pdf Thymic selection and peripheral activation of CD8 T cells by the same class I MHC/peptide complex JD Mintern , MM Maurice , HL Ploegh - The Journal of , 2004 - journals.aai.orghttps://journals.aai.org/jimmunol/article/172/1/699/71907 Positive and negative selection invoke distinct signaling pathways. J Alberola-Ila, KA Hogquist , KA Swan - The Journal of , 1996 - rupress.orghttps://rupress.org/jem/article-abstract/184/1/9/50745 Mouse MHC class I tetramers that are unable to bind to CD8 reveal the need for CD8 engagement in order to activate naive CD8 T cells E Schott, HL Ploegh - European journal of immunology, 2002 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/1521-4141(200212)32:12%3C3425::AID-IMMU3425%3E3.0.CO;2-7 CD8 cell division maintaining cytotoxic memory occurs predominantly in the bone marrow E Parretta, G Cassese, P Barba, A Santoni - The journal of , 2005 - journals.aai.orghttps://journals.aai.org/jimmunol/article/174/12/7654/37011 Phage display of a CTL epitope elicits a long-term in vivo cytotoxic response D Mascolo, P Barba, P De Berardinis - FEMS Immunology & , 2007 - academic.oup.comhttps://academic.oup.com/femspd/article-abstract/50/1/59/505439 Targeted Therapy Combined with Immune Modulation Using Gold Nanoparticles for Treating Metastatic Colorectal Cancer B Moriarity , T Starr, E Pomeroy , M Crosby, W Durose - 2017 - apps.dtic.milhttps://apps.dtic.mil/sti/citations/AD1070327 CD8 lineage commitment in the absence of CD8 AW Goldrath , KA Hogquist , MJ Bevan - Immunity, 1997 - cell.comhttps://www.cell.com/immunity/pdf/S1074-7613(00)80351-9.pdf HIV-1 Gag p17 presented as virus-like particles on the E2 scaffold from Geobacillus stearothermophilus induces sustained humoral and cellular immune A Caivano , NA Doria-Rose, B Buelow, R Sartorius - Virology, 2010 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0042682210005568

Peptide H-SSIMR-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-SSIMR-OH include the following: Mass spectrometry in virological sciences A Milewska , J Ner-Kluza, A Dabrowska - Mass spectrometry , 2020 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/mas.21617

A synthetic peptide for use as a blocking control in assays to test for specificity of RAB22A antibody, catalog no. 70R-4379

Peptide H-LDEETGEFL-NH2 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-LDEETGEFL-NH2 include the following: Design and synthesis of disulfide-rich peptides with orthogonal disulfide pairing motifs Z Huang, Y Wu, H Dong, Y Zhao - The Journal of Organic , 2020 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.joc.0c01600 Kinetic analyses of Keap1-Nrf2 interaction and determination of the minimal Nrf2 peptide sequence required for Keap1 binding using surface plasmon resonance Y Chen, D Inoyama, ANT Kong - Chemical biology & , 2011 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1747-0285.2011.01240.x Exploring the binding of rationally engineered tandem-repeat proteins to E3 ubiquitin ligase Keap1 SK Madden , LS Itzhaki - Protein Engineering, Design and , 2021 - academic.oup.comhttps://academic.oup.com/peds/article-abstract/doi/10.1093/protein/gzab027/6457287 Small molecule modulators of K eap1-N rf2-ARE pathway as potential preventive and therapeutic agents S Magesh, Y Chen, L Hu - Medicinal research reviews, 2012 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/med.21257 Activators and inhibitors of NRF2: a review of their potential for clinical development N Robledinos-Anton - Oxidative medicine , 2019 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1155/2019/9372182 The Keap1-Nrf2-ARE pathway as a potential preventive and therapeutic target: an update MC Lu, JA Ji, ZY Jiang, QD You - Medicinal research reviews, 2016 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/med.21396 Interaction energetics and druggability of the protein-protein interaction between Kelch-like ECH-Associated Protein 1 (KEAP1) and Nuclear Factor Erythroid 2 Like 2 M Zhong , A Lynch, SN Muellers, S Jehle, L Luo - Biochemistry, 2019 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.biochem.9b00943 Prediction of binding energy of Keap1 interaction motifs in the Nrf2 antioxidant pathway and design of potential high-affinity peptides M Karttunen , WY Choy , EA Cino - The Journal of Physical , 2018 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jpcb.8b03295 Inhibiting the Keap1/Nrf2 Protein-Protein Interaction with Protein-Like Polymers KP Carrow, HL Hamilton, MP Hopps, Y Li - Advanced , 2024 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/adma.202311467 Virtual screening expands the non-natural amino acid palette for peptide optimization KN Amarasinghe , L De Maria, C Tyrchan - Journal of Chemical , 2022 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jcim.2c00193 Combined peptide and small-molecule approach toward nonacidic THIQ inhibitors of the KEAP1/NRF2 interaction JM Ontoria, I Biancofiore, P Fezzardi - ACS Medicinal , 2020 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acsmedchemlett.9b00594 Peptide Macrocycles Developed from Precisely Regulated Multiple Cyclization of Unprotected Peptides J Wang, M Zha, Q Fei, W Liu, Y Zhao - Chemistry-A European , 2017 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201703139 Novel protein-protein interaction inhibitor of Nrf2-Keap1 discovered by structure-based virtual screening HP Sun , ZY Jiang, MY Zhang, MC Lu, TT Yang - , 2014 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2014/md/c3md00240c A Case Study on the Keap1 Interaction with Peptide Sequence Epitopes Selected by the Peptidomic mRNA Display H Hirose , T Hideshima, T Katoh , H Suga - ChemBioChem, 2019 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.201900039 Peptide and small molecule inhibitors of the Keap1-Nrf2 protein-protein interaction G Wells - Biochemical Society Transactions, 2015 - portlandpress.comhttps://portlandpress.com/biochemsoctrans/article-abstract/43/4/674/88607 Discovery of direct inhibitors of Keap1-Nrf2 protein-protein interaction as potential therapeutic and preventive agents DA Abed, M Goldstein, H Albanyan, H Jin - Acta Pharmaceutica Sinica , 2015 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S2211383515000829 Strategies for converting turn-motif and cyclic peptides to small molecules for targeting protein-protein interactions D Hayward, AM Beekman - RSC Chemical Biology, 2024 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2024/cb/d3cb00222e Structural Basis for the Nrf2 interaction with the Keap1 repressor B Padmanabhan, KI Tong, Y Nakamura, A Kobayashi - researchgate.nethttps://www.researchgate.net/profile/Akira-Kobayashi-3/publication/266354656_Structural_Basis_for_the_Nrf2_interaction_with_the_Keap1_repressor/links/55b3215308aed621ddfe17f0/Structural-Basis-for-the-Nrf2-interaction-with-the-Keap1-repressor.pdf

Muscarinic toxin 3 (MT3), a potent non-competitive antagonist of mAChR and adrenoceptors, exhibits pIC50 values of 6.71 for M1, 8.79 for M4, 8.86 for α1A, 7.57

Peptide H-VLRPGGHFL-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-VLRPGGHFL-OH include the following: Delivery of Mycobacterium tuberculosis epitopes by Bordetella pertussis adenylate cyclase toxoid expands HLA-E-restricted cytotoxic CD8+ T cells GD Badami, MP La Manna , P Di Carlo - Frontiers in , 2023 - frontiersin.orghttps://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1289212

Fmoc-Cys((R)-2,3-di(palmitoyloxy)-propyl)-OH is a versatile building block that is useful for the synthesis of complex compounds. This compound has been shown to be a useful intermediate in the synthesis of pharmaceuticals, organic dyes and research chemicals. Fmoc-Cys((R)-2,3-di(palmitoyloxy)-propyl)-OH is a fine chemical that is used as a reagent in organic synthesis. It has CAS No. 139573-77-6 and can be used as a speciality chemical or reaction component.

Angiotensin II (Human) is a peptide that is produced by the renin-angiotensin system. It has been shown to be an effective inhibitor of the cell adhesion molecule CD44, and can also stimulate the proliferation of cells in culture. Angiotensin II (Human) is a ligand for angiotensin receptors, which are found on many different types of cells. The binding of angiotensin II to these receptors stimulates the production of cyclic AMP, which causes vasoconstriction and increased blood pressure.

Peptide H-DNEAYEMPSEEGYQD-NH2 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-DNEAYEMPSEEGYQD-NH2 include the following: CD4+ T cells contribute to neurodegeneration in Lewy body dementia D Gate , E Tapp, O Leventhal, M Shahid , TJ Nonninger - Science, 2021 - science.orghttps://www.science.org/doi/abs/10.1126/science.abf7266

A synthetic peptide for use as a blocking control in assays to test for specificity of FANCE antibody, catalog no. 70R-2296

Peptide H-LPVVLENARILKNCVDAK-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-LPVVLENARILKNCVDAK-OH include the following: Persistent central memory phenotype of circulating Fel d 1 peptide/DRB1∗ 0101 tetramer-binding CD4+ T cells EAL Bateman , MR Ardern-Jones , GS Ogg - Journal of allergy and clinical , 2006 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0091674906015922

Peptide H-LNVTEQEK^-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-LNVTEQEK^-OH include the following: Mass spectrometry analysis of the post-translational modifications of alpha-enolase from pancreatic ductal adenocarcinoma cells W Zhou, M Capello , C Fredolini - Journal of proteome , 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/pr901109w A clean, more efficient method for in-solution digestion of protein mixtures without detergent or urea SC Kim , Y Chen , S Mirza , Y Xu, J Lee - Journal of proteome , 2006 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/pr0603396 Pushing the boundaries of sensitivity and depth-of-coverage for nanoflow proteomics P Pribil, S Tate, I Batruch - sciex.comhttps://sciex.com/content/dam/SCIEX/pdf/tech-notes/life-science-research/MKT-29730-A_TN_Pushing_sensitivity-depth_of_coverage_boundaries_using_IonOpticks_and_Zeno_SWATH_DIA-FINAL_20231025.pdf Improved data-independent acquisition (DIA) and data-dependent acquisition (DDA) performance on low-level proteomic samples using a novel Zeno trap K Tran, I Batruch, S Tate, N Bloomfield, A Chelur - antisel.grhttps://antisel.gr/wp-content/uploads/2023/08/2023-US-HUPO_Improved-DIA-and-DDA-performance-on-low-level-proteomic-samples-using-a-novel-Zeno-trap.pdf Improved data-independent acquisition (DIA) and data-dependent acquisition (DDA) performance on low-level proteomic samples using a novel Zeno trap I Batruch, S Tate, N Bloomfield, A Chelur - sciex.comhttps://sciex.com/content/dam/SCIEX/pdf/posters/amer/asms2022/lifescienceresearch/077_monday_batruch.pdf

NHS-dPEG®4 Biotin is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. NHS-dPEG®4 Biotin is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

A synthetic peptide for use as a blocking control in assays to test for specificity of Dtx3 antibody, catalog no. 70R-8562

A synthetic peptide for use as a blocking control in assays to test for specificity of Scamp1 antibody, catalog no. 70R-9784

Allatostatin IV, an insect octapeptide, regulates juvenile hormone synthesis.

A synthetic peptide for use as a blocking control in assays to test for specificity of DDX39 antibody, catalog no. 70R-1399

Custom research peptide; min purity 95%. For different specs please use the Peptide Quote Tool

Peptide Biot-PLARTLSVAGLPGKK-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 Biot-PLARTLSVAGLPGKK-OH include the following: Peptide sequence influence on the differentiation of valine and norvaline by hot electron capture dissociation Z Liang , X Yu, W Zhong - Analytical chemistry, 2019 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.8b04808 Protein kinase D2 mediates lysophosphatidic acid-induced interleukin 8 production in nontransformed human colonic epithelial cells through NF-κB TT Chiu, WY Leung, MP Moyer - of Physiology-Cell , 2007 - journals.physiology.orghttps://journals.physiology.org/doi/abs/10.1152/ajpcell.00308.2006 Calmodulin-dependent protein kinase II mediates inactivation of MPF and CSF upon fertilization of Xenopus eggs T Lorca, FH Cruzalegui, D Fesquet, J Cavadore, J Mery - Nature, 1993 - nature.comhttps://www.nature.com/articles/366270a0 CCK2 (CCKB/gastrin) receptor mediates rapid protein kinase D (PKD) activation through a protein kinase C-dependent pathway T Chiu, E Rozengurt - FEBS letters, 2001 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0014579301020762 In vitro activation and substrates of recombinant, baculovirus expressed human protein kinase Cu S Dieterich, T Herget, G Link, H Böttinger - FEBS , 1996 - Wiley Online Libraryhttps://febs.onlinelibrary.wiley.com/doi/abs/10.1016/0014-5793(96)00116-0 Phosphorylation and activation of Ca2+-calmodulin-dependent protein kinase IV by Ca2+-calmodulin-dependent protein kinase Ia kinase: Phosphorylation of MA Selbert, KA Anderson, QH Huang - Journal of Biological , 1995 - ASBMBhttps://www.jbc.org/article/S0021-9258(18)95656-5/abstract Intersubunit capture of regulatory segments is a component of cooperative CaMKII activation LH Chao , P Pellicena , S Deindl , LA Barclay - Nature structural & , 2010 - nature.comhttps://www.nature.com/articles/nsmb.1751 Nostocyclopeptide-M1: A potent, nontoxic inhibitor of the hepatocyte drug transporters OATP1B3 and OATP1B1 L Herfindal , L Myhren , R Kleppe - Molecular , 2011 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/mp1002224 Insulin activates the kinase activity of the Raf-1 proto-oncogene by increasing its serine phosphorylation. KS Kovacina, K Yonezawa, DL Brautigan - Journal of Biological , 1990 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0021925819383152 Biochemical characterization of FIKK8-a unique KOHJL Wei, QV Brand - parasitology, 2008 - researchgate.nethttps://www.researchgate.net/profile/Verena-Brand-2/publication/279302367_Biochemical_characterization_of_FIKK8_-_A_unique_protein_kinase_from_the_malaria_parasite_Plasmodium_falciparum_and_other_apicomplexans/links/55f0bba708aef559dc46df91/Biochemical-characterization-of-FIKK8-A-unique-protein-kinase-from-the-malaria-parasite-Plasmodium-falciparum-and-other-apicomplexans.pdf A requirement of hydrophobic and basic amino acid residues for substrate recognition by Ca2+/calmodulin-dependent protein kinase Ia. JC Lee, YG Kwon , DS Lawrence - Proceedings of the , 1994 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.91.14.6413 Expression and Characterization of PKD, a Phorbol Ester and Diacylglycerol-stimulated Serine Protein Kinase (∗) J Van Lint , J Sinnett-Smith, E Rozengurt - Journal of Biological Chemistry, 1995 - ASBMBhttps://www.jbc.org/article/S0021-9258(18)83023-X/abstract Direct activation of the serine/threonine kinase activity of Raf-1 through tyrosine phosphorylation by the PDGF beta-receptor DK Morrison, DR Kaplan , JA Escobedo, UR Rapp - Cell, 1989 - cell.comhttps://www.cell.com/cell/pdf/0092-8674(89)90100-1.pdf Structures of apicomplexan calcium-dependent protein kinases reveal mechanism of activation by calcium AK Wernimont, JD Artz , P Finerty Jr, YH Lin - Nature structural & , 2010 - nature.comhttps://www.nature.com/articles/nsmb.1795 Pseudosubstrate inhibition of CDPK, a protein kinase with a calmodulin-like domain AC Harmon, BC Yoo, C McCaffery - Biochemistry, 1994 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/bi00189a032 An enzyme-linked immunosorbent assay for protein kinase D activity using phosphorylation site-specific antibodies A Rykx, S Vancauwenbergh , L De Kimpe - Assay and drug , 2007 - liebertpub.comhttps://www.liebertpub.com/doi/abs/10.1089/adt.2007.081

A synthetic peptide for use as a blocking control in assays to test for specificity of Pxmp3 antibody, catalog no. 70R-8552

Peptide Ac-CETVSTQELYS-NH2 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 Ac-CETVSTQELYS-NH2 include the following: Functional Analysis of Chk2-Kiaa0170 Interaction Z Lou, MAYO CLINIC ROCHESTER MN - 2004 - apps.dtic.milhttps://apps.dtic.mil/sti/citations/tr/ADA462752 MDC1 is coupled to activated CHK2 in mammalian DNA damage response pathways Z Lou, K Minter-Dykhouse, X Wu, J Chen - Nature, 2003 - nature.comhttps://www.nature.com/articles/nature01447

A synthetic peptide for use as a blocking control in assays to test for specificity of ALOX15B antibody, catalog no. 70R-1635

Key subunit of extracellular plaques found in the brains of patients with Alzheimer's disease. TFA salt; 95%.

Peptide H-EFFVGLSK^-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-EFFVGLSK^-OH include the following: Dexamethasone regulates cochlear expression of deafness-associated proteins myelin protein zero and heat shock protein 70, as revealed by iTRAQ proteomics Y Maeda, K Fukushima, S Kariya, Y Orita - Otology & , 2015 - journals.lww.comhttps://journals.lww.com/otology-neurotology/FullText/2015/08000/Dexamethasone_Regulates_Cochlear_Expression_of.19.aspx

A synthetic peptide for use as a blocking control in assays to test for specificity of RIOK1 antibody, catalog no. 70R-10128

Preprosomatostatin (25-34) is a peptide.

Peptide H-R^GFFYTPKT-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-R^GFFYTPKT-OH include the following: Solid phase isotope exchange of deuterium and tritium for hydrogen in human recombinant insulin YA Zolotarev, AK Dadayan, VS Kozik - Russian Journal of , 2014 - Springerhttps://link.springer.com/article/10.1134/S1068162014010154 The investigation on Resorcinarenes towards either inhibiting or promoting insulin fibrillation X Han , C Tian , I Gandra, V Eslava - A European Journal, 2017 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201704932 Multiplexed quantification of insulin and C-peptide by LC-MS/MS without the use of antibodies N Foulon, E Goonatilleke, MJ MacCoss - Journal of Mass , 2022 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S2667145X22000189 Preparation and Evaluation of Molecular Imaging Probes for Breast Cancer M ElGamal - 2014 - macsphere.mcmaster.cahttps://macsphere.mcmaster.ca/handle/11375/16037 Synthesis and in Vitro Evaluation of 18F- and 19F-Labeled Insulin: A New Radiotracer for PET-based Molecular Imaging Studies KJ Guenther, S Yoganathan , R Garofalo - Journal of medicinal , 2006 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm0509344 Mesalazine inhibits amyloid formation and destabilizes pre-formed amyloid fibrils in the human insulin F Bardineshin, S Bahramikia , R Khodarahmi - Journal of , 2023 - Springerhttps://link.springer.com/article/10.1007/s10895-022-03142-7 Synthesis and characterization of rhenium and technetium-99m labeled insulin C Sundararajan, TR Besanger, R Labiris - Journal of medicinal , 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm100096c IGF Comparative Sequence Chart B Domain, C Domain, A Domain, D Domain - gropep.comhttps://gropep.com/wp-content/uploads/2023/08/GroPep_Comp_Chart-IGFs.pdf Aquaculture IGF Sequence Chart B Domain, C Domain, A Domain, D Domain - gropep.comhttps://gropep.com/wp-content/uploads/2023/08/GroPep_Aqua_Chart.pdf

Peptide H-AAFEFINSL-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-AAFEFINSL-OH include the following: Analysis of A47, an Immunoprevalent Protein of Vaccinia Virus, Leads to a Reevaluation of the Total Antiviral CD8+ T Cell Response TJ Yuen, IEA Flesch, NA Hollett, BM Dobson - Journal of , 2010 - Am Soc Microbiolhttps://journals.asm.org/doi/abs/10.1128/jvi.01281-10

Bz-Arg-OEt • HCl (BAEE) is a peptide substrate of trypsin. It is an enzyme that cleaves proteins by hydrolyzing the peptide bonds at the carboxyl termini of polypeptides. The Bz-Arg-OEt • HCl (BAEE) reacts with trypsin to form a complex that has a unique spectrum of absorption and emission maxima, which can be used to identify BAEE in solution.

Peptide Ac-TYFAVLM-NH2 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 Ac-TYFAVLM-NH2 include the following: Allosteric modulation of tethered ligand-activated G protein-coupled receptors VM Mirka, R Ramachandran - Allosteric Modulation of G Protein-Coupled , 2022 - Elsevierhttps://www.sciencedirect.com/science/article/pii/B9780128197714000026 Creating Tools to Study the Signaling and Function of the Adhesion Family of GPCRs VM Mirka - 2021 - search.proquest.comhttps://search.proquest.com/openview/f8d212dbb311ee6e9210f9ef4b70ecd9/1?pq-origsite=gscholar&cbl=18750&diss=y SNAP-tag-enabled super-resolution imaging reveals constitutive and agonist-dependent trafficking of GPR56 in pancreatic beta-cells OE Olaniru , J Cheng, J Ast , A Arvaniti, P Atanes - Molecular , 2021 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S2212877821001307 Downstream signalling of the disease-associated mutations on GPR56/ADGRG1 O CevheroÄŞlu , N Demir, MS Kesici - Basic & clinical , 2023 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/bcpt.13873 Roles of focal adhesion kinase PTK2 and integrin alphaIIbbeta3 signaling in collagen-and GPVI-dependent thrombus formation under shear J Huang , NJ Jooss, DI Fernandez, A Sickmann - International journal of , 2022 - mdpi.comhttps://www.mdpi.com/1422-0067/23/15/8688 Adhesion G protein-coupled receptors are activated by exposure of a cryptic tethered agonist HM Stoveken , AG Hajduczok , L Xu - Proceedings of the , 2015 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.1421785112 Re-routing GPR56 signalling using Galpha12/13 G protein chimeras F Faas, A Norskov, PJ Holst - Basic & Clinical , 2023 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/bcpt.13935 The role of GPR56/ADGRG1 in health and disease AK Singh , HH Lin - biomedical journal, 2021 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S2319417021000445

Custom research peptide; min purity 95%. For different specs please use the Peptide Quote Tool

Peptide H-AIEDYINEFSVR-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-AIEDYINEFSVR-OH include the following: Exploring biological and geological age-related changes through variations in intra-and intertooth proteomes of ancient dentine N Procopio , AT Chamberlain - Journal of proteome , 2018 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jproteome.7b00648

A synthetic peptide for use as a blocking control in assays to test for specificity of SIDT2 antibody, catalog no. 70R-7049

H-Ala-Tyr-Pro-Gly-Lys-Phe-NH2 is a selective inhibitor of aminopeptidase N. It has been shown to inhibit neutrophil and leukocyte recruitment in rat peritonitis models, as well as to reduce the severity of carrageenan induced paw edema in rats. H-Ala-Tyr-Pro-Gly-Lys-Phe NH2 also inhibits the activation of platelets by aspirin and reduces their aggregation, which may be due to inhibition of PAR4. PAR4 is a G protein coupled receptor that is activated by proteases such as thrombin and trypsin. Activation of PAR4 induces proinflammatory cytokines, leading to increased leukocyte recruitment and inflammation.

Peptide H-WMTNNPPIPVGEIYK-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-WMTNNPPIPVGEIYK-OH include the following: Identification of circulating antigen-specific CD4+ T lymphocytes with JM Newton, CR Mackay, DA Cooper, NK Saksena - academia.eduhttps://www.academia.edu/download/42745742/Identification_of_circulating_antigen-sp20160216-13262-wgqv7u.pdf Identification of circulating antigen-specific CD4+ T lymphocytes with a CCR5+, cytotoxic phenotype in an HIV-1 long-term nonprogressor and in CMV infection JJ Zaunders , WB Dyer , B Wang, ML Munier - Blood, 2004 - ashpublications.orghttps://ashpublications.org/blood/article-abstract/103/6/2238/18356 Possible clearance of transfusion-acquired nef/LTR-deleted attenuated HIV-1 infection by an elite controller with CCR5 Δ32 heterozygous and HLA-B57 J Zaunders , WB Dyer , M Churchill , CML Munier - Journal of virus , 2019 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S205566402030056X

Peptide H-TTPPV^LDSDGSFFLYSR^-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-TTPPV^LDSDGSFFLYSR^-OH include the following: Absolute quantitation of immunoglobulin G and its glycoforms using multiple reaction monitoring Q Hong , CB Lebrilla , S Miyamoto - Analytical chemistry, 2013 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac4009995 Method limitations in LC-MS/MS and immunonephelometric measurement of IgG subclasses G van der Gugten , A Mattman , G Ritchie - Clinical , 2021 - academic.oup.comhttps://academic.oup.com/clinchem/article-abstract/67/2/440/6040699 Development of an LC-MS/MS method for absolute quantification of IgG4 by evaluating dependence on the digestion efficiency using a non-cleavable/dually D Sasaki, H Kashiwagura, Y Teruuchi - Biochemical and Biophysical , 2023 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0006291X23011737 Absolute and multiplex quantification of antibodies in serum using PSAQ™standards and LC-MS/MS D Lebert, G Picard, C Beau-Larvor, L Troncy - Bioanalysis, 2015 - Future Sciencehttps://www.future-science.com/doi/abs/10.4155/bio.15.56

Peptide Ac-LDDRHDDGLDDMKDEEY-NH2 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 Ac-LDDRHDDGLDDMKDEEY-NH2 include the following: BMS-345541 is a highly selective inhibitor of IκB kinase that binds at an allosteric site of the enzyme and blocks NF-κB-dependent transcription in mice JR Burke, MA Pattoli, KR Gregor, PJ Brassil - Journal of Biological , 2003 - ASBMBhttps://www.jbc.org/article/S0021-9258(19)31057-9/abstract The catalytic subunits of IκB kinase, IKK-1 and IKK-2, contain non-equivalent active sites when expressed as homodimers JR Burke, J Strnad - Biochemical and biophysical research communications, 2002 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0006291X02004175

Peptide H-SITSAVLQSGFRKMA-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-SITSAVLQSGFRKMA-OH include the following: Screening of drugs by FRET analysis identifies inhibitors of SARS-CoV 3CL protease YC Liu, V Huang, TC Chao , CD Hsiao, A Lin - Biochemical and , 2005 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0006291X0501051X Steady-State and Pre-Steady-State Kinetic Evaluation of Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) 3CLpro Cysteine Protease: Development of J Solowiej, JA Thomson, K Ryan, C Luo, M He - Biochemistry, 2008 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi702107v

A synthetic peptide for use as a blocking control in assays to test for specificity of MDH2 antibody, catalog no. 70R-1090

A synthetic peptide for use as a blocking control in assays to test for specificity of NUP155 antibody, catalog no. 70R-3056

A synthetic peptide for use as a blocking control in assays to test for specificity of C19orf25 antibody, catalog no. 70R-8036

Peptide H-SPGVAELSLR^-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-SPGVAELSLR^-OH include the following: Critical issues and optimized practices in quantification of protein abundance level to determine interindividual variability in DMET proteins by LC-MS/MS proteomics DK Bhatt , B Prasad - Clinical Pharmacology & Therapeutics, 2018 - Wiley Online Libraryhttps://ascpt.onlinelibrary.wiley.com/doi/abs/10.1002/cpt.819

Custom research peptide; min purity 95%.

Potent NK2 agonist, EC50=3.7 nM in rat colon; >1000x selectivity over NK1, >300x over NK3; effective in vivo.

A synthetic peptide for use as a blocking control in assays to test for specificity of ZNF12 antibody, catalog no. 20R-1099