H-KSKK-OH

Ref. 3D-PP44929

Información del producto

• Nombre: H-KSKK-OH
• Sinónimos: NH2-Lys-Ser-Lys-Lys-OH

Descripción

Peptide H-KSKK-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-KSKK-OH include the following: Construction and identification of human tissue kallikrein gene eukaryotic expressing vector Y Dai , W Peng, T Li, H Du, W Sun, D Chen - Journal of Huazhong , 2007 - Springerhttps://link.springer.com/article/10.1007/s11596-007-0214-y Divergent modulation of proteostasis in prostate cancer P Ballar Kirmizibayrak , B Erbaykent-Tepedelen - and Disease: From , 2020 - Springerhttps://link.springer.com/chapter/10.1007/978-3-030-38266-7_5 X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions NS Heiss, SW Knight, TJ Vulliamy , SM Klauck - Nature , 1998 - nature.comhttps://www.nature.com/articles/ng0598-32 The Helix-Loop-Helix motif of human EIF3A regulates translation of proliferative cellular mRNAs MP Volegova, C Hermosillo, JHD Cate - Plos one, 2023 - journals.plos.orghttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0292080 GFI1 snag domain methylation directs LSD1 recruitment to control transcription and cell fate determination in hematopoiesis ME Velinder , J Singer, J Meznarich, ER Theisen - Blood, 2015 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0006497118470255 Methylation and sumoylation regulate LSD1-corest recruitment and activity to control transcriptional and cellular functions of GFI1 ME Velinder - 2016 - search.proquest.comhttps://search.proquest.com/openview/154f4525a1230181db44df78f9070478/1?pq-origsite=gscholar&cbl=18750 Molecular cloning of cDNA for murine interleukin-3 MC Fung, AJ Hapel , S Ymer, DR Cohen , RM Johnson - Nature, 1984 - nature.comhttps://www.nature.com/articles/307233a0 GFI1 functions in transcriptional control and cell fate determination require SNAG domain methylation to recruit LSD1 M Velinder , J Singer, D Bareyan - Biochemical , 2016 - portlandpress.comhttps://portlandpress.com/biochemj/article-abstract/473/19/3355/49691 Sequential activation of ICE-like and CPP32-like proteases during Fas-mediated apoptosis M Enari, RV Talanian , WW Wrong, S Nagata - Nature, 1996 - nature.comhttps://www.nature.com/articles/380723a0 Regulation of the androgen receptor by SET9-mediated methylation L Gaughan , J Stockley , N Wang - Nucleic acids , 2011 - academic.oup.comhttps://academic.oup.com/nar/article-abstract/39/4/1266/1008015 Genome-wide analyses of carboxyl-terminal sequences JJ Chung , H Yang, M Li - Molecular & Cellular Proteomics, 2003 - ASBMBhttps://www.mcponline.org/article/S1535-9476(20)34463-7/fulltext Activity Guided Azide-methyllysine Photo-trapping for Substrate Profiling of Lysine Demethylases J Kuwik, K Hinkelman, M Waldman - Journal of the , 2023 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jacs.3c07299 The transcription factors GFI1 and GFI1B as modulators of the innate and acquired immune response J Fraszczak, T Möröy - Advances in immunology, 2021 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0065277621000031 A short Gfi-1B isoform controls erythroid differentiation by recruiting the LSD1-CoREST complex through the dimethylation of its SNAG domain B Laurent , V Randrianarison-Huetz - Journal of cell , 2012 - journals.biologists.comhttps://journals.biologists.com/jcs/article-abstract/125/4/993/33192

• Marca: Biosynth