Transfection Reagents
Sigma Aldrich Fine Chemicals Biosciences 1 VIAL HUH-7D 12 CELL LINE HUM
NC3659956 1 VIAL HUH-7D 12 CELL LINE HUM
Genesee Scientific Corporation TRANSFCTN REAGNT 1.5ML/4X60BUF
Transfection Reagent with 4 x 60ml Buffer1.5ml/UnitBrand: Polyplus-transfectionBest-in-Class DNA Transfection ReagentBased on Novel Cationic NanotechnologyReach Maximal Gene Expression in Hard-to-Transfect CellsExcellent Cell Viability & MorphologyHighly Efficient: Requires Minimal Reagent & DNAReady-to-Use ProtocolCost Effective
Apexbio Technology LLC Lipo2K Transfection Reagent 1.5ml
Lipo2K Transfection Reagent is a cationic liposome-based transfection reagent widely used for cell transfections capable of effectively delivering DNA or RNA (such as siRNA/mRNA) into various cell types (adherent or suspension cells) This reagent provides advantages including high transfection efficiency simple operation good reproducibility and minimal cytotoxicity Furthermore it is suitable not only for single plasmid or siRNA transfection but also for co-transfection applications involving multiple plasmids or combinations of plasmids with siRNAs To achieve optimal transfection outcomes it is recommended to use serum-containing medium without antibiotics during the transfection process Typically expression analysis after plasmid transfection can be performed 24 48 hours post-transfection while analysis after siRNA transfection is recommended to be carried out after 3 5 days
HORIZON DISCOVERY BIOSCIENCES LIMITED ACCELL CYCLOPHILIN B HM 5NMOL
Accell Cyclophilin B Control Pool HUMAN 5nmol
STEMCELL Technologies ReproRNA™-OKSGM, Size: 12 µg
ReproRNA™-OKSGM is a single-stranded RNA replicon vector that contains five reprogramming factors: OCT4, KLF-4, SOX2, GLIS1, and c-MYC, as well as a puromycin-resistance gene (Figure 1). This RNA vector reprograms somatic cells, such as fibroblasts, into induced pluripotent stem (iPS) cells with high efficiency and only requires a single transfection step (Figure 2). When used together with ReproTeSR™ reprogramming medium, the generation of iPS cell colonies can be achieved under feeder-free conditions with superior colony morphology and similar reprogramming efficiency to feeder-based systems (Figures 3 - 4). ReproRNA™-derived iPS cell colonies also express markers of undifferentiated cells and retain a normal karyotype (Figures 5-6). Subsequently, iPS cells generated with ReproRNA™-OKSGM can be maintained in TeSR™ maintenance media (mTeSR™1, TeSR™2, or TeSR™-E8™)