WebSH-SY5Y. CRL-2266 ™. The SH-SY5Y cell line is a thrice cloned subline of the neuroblastoma cell line SK-N-SH ( ATCC HTB-11 ), which was established in 1970 from a metastatic bone … WebTrans-Booster is a highly effective reagent to enhance the transfection efficiency in different cell types. Trans-Booster is a synthetic polymer that is specifically tailored for DNA delivery. Co-incubation with DNA molecules and RJH transfection reagents results in 100-200 nm particles with a net charge that depends on the relative ratio of ...
FuGENE® HD Transfection Reagent - Promega
WebApr 11, 2024 · Cell Culture and siRNA Transfection. Human-derived glioma cell line, U87MG, and human-derived neuroblastoma cell line, SH-SY5Y, were cultured in Dulbecco's modified Eagle's medium with 10% fetal bovine serum, penicillin/streptomycin, and l-glutamine.We used the Silencer Select siRNA (Life Technologies, Carlsbad, CA) directed against human … WebSeveral gene delivery reagents were analyzed for their transfection efficiency. Genes studied belonged to the class of mammalian proteins termed regulators of G-protein signaling … slow it down roddy
Does anyone have experience transfecting SH-SY5Y cells ...
Weband SHSY5Y cells (neuroblastoma) in a 24-well format. For Gibco ™ Human Neural Stem Cells (hNSCs), 250 ng/well of mRNA was used in a 48-well format. Results are compared to plasmid DNA delivered with the leading DNA transfection reagent. GFP expression was analyzed 24 hours posttransfection. High transfection efficiency for neural cell models WebAFBs were expressed in i36 cells and transfection efficiency was assayed as ratio of CFP or YFP positive cells over total number of cells in the bright field. ( A ) Confocal images of i36 cells transfected with inter-AFB ER, inter-AFB or intra-AFB were acquired in bright field, in CFP and YFP channel with a Leica confocal microscope SP2, using a 40 x oil objective. WebNov 14, 2024 · Here, the transfection with miR-15b mimics significantly reduced the reporter activity of NF-κB1 and IKK-α (Figure 6A,D). As reported, putative binding sites for miR-15b were identified in the 3′UTRs of NFKB1 and IKK-α ( Figure 6 C,F). miR-15b failed to regulate either NF-κB1 or IKK-α transcription when the mutation within the corresponding 3′UTRs … software non compete agreement