WebArticle Snippet: Once this larger ORF was constructed, FLRAG1 and subsequent truncations were cloned into the pRetroX-TRE3G (Clontech)-inducible vector using In-Fusion cloning (Takara). mCherry constructs were generated by insertion of mouse FLR1, core RAG1, ∆215, and dNOL ORFs into the mCherry2-C1 vector (54563, AddGene) using In-Fusion. Web17 jan. 2024 · As a control for transfection efficiency, mCherry2-C1 was employed. The fluorescent intensity of humanized mNeonGreen was significantly increased (1.39 ± 0.06-fold, p<0.01) compared with that of original mNeonGreen, while there is no significant difference of that of mCherry2 ( Fig 2 ).
mCherry2 Sequence and Map - SnapGene
WebVector for fusing mCherry to the N-terminus of a partner protein. WebiLab Organizer :: login. Ilab Software Help System Status Request Demo. Sign in using Chapman University credentials. or. Sign in using iLab credentials. or. Sign in using other institution credentials. or. Agilent Employees: sign in using Agilent SSO credentials. edgewick inn snoqualmie
mCherry2 N1 Clone 1 CMV - Addgene
Web7 jan. 2024 · Product Name : mCherry2-N1 article : bacterial resistance : Kanamycin cloning : growth notes : . Excitation = 587; Emission = 610 growth strain : Localization: N1 … WebPlasmid p-mCherry2-sgRNA (empty) from Dr. Sarah McClelland's lab contains the insert U6-sgRNA(F+E) empty and is published in 10.15252/embj.2024111587 This plasmid is available through Addgene. WebpmCherry2-GNB1-T2A-mCherry2-GNG2-IRES-GNAI1-mEYFP (Q69K) Plasmid. #190755. Purpose. Expression of trimeric G protein with mCherry2 (GNB1 and GNG2) or mEYFP … edgewick motel north bend