LipoFectMax™ 3000 Transfection Reagent is a lipid-based transfection reagent that forms a complex with DNA or RNA, and transports the complex into a variety of adherent and suspension cell lines. LipoFectMax™ 3000 Transfection Reagent delivers superior transfection efficiency and improved cell viability for the widest range of hard-to-transfect and common cells. This reagent has been tested to work the same efficiency as Lipofectamine® 3000 Reagent, and used for the transfection of both DNA and RNA into eukaryotic cells even in the presence of serum.
Cited Reference:
Bioinformatics analysis of LINC01554 and its co‑expressed genes in hepatocellular carcinoma
Sesterterpene MHO7 suppresses breast cancer cells as a novel estrogen receptor degrader
Generation of C-to-G transversion in mouse embryos via CG editors
RIPK3 Promotes JEV Replication in Neurons via Downregulation of IFI44L
Stanniocalcin 2 Is Upregulated by Calcium-Sensing Receptor and Protects Human Vascular Smooth Muscle Cells from High-Phosphate-Induced Apoptosis
STC2: A Novel and Regulable Protector of Vascular Smooth Muscle Cells
Axl-/- neurons promote JEV infection by dampening the innate immunity
Endothelial and systemic upregulation of miR-34a-5p fine-tunes senescence in progeria.
A novel homozygous RIPK4 variant in a family with severe Bartsocas-Papas syndrome
Comprehensive Pan-Cancer Analyses of Immunogenic Cell Death as a Biomarker in Predicting Prognosis and Therapeutic Response.
Hydroxychloroquine impairs mTORC1-dependent cholesterol biosynthesis and sensitizes retinal pigment epithelial cells to UV-induced cell death
PTPRH Alleviates Airway Obstruction and Th2 Inflammation in Asthma as a Protective Factor
Human cytomegalovirus pUL97 upregulates SOCS3 expression via transcription factor RFX7 in neural progenitor cells
Comprehensive Pan-Cancer Analyses of Immunogenic Cell Death as a Biomarker in Predicting Prognosis and Therapeutic Response.
Features
Figure 1. Assessment of LipoFectMax™ 3000 and LipoFectMax™ transfection efficiencies using GFP visualization. A549, NIH3T3, HepG2, and MCF7 cell lines were transfected with a GFP-expressing plasmid using the indicated transfection reagents. Cells were visualized 48 hours post-transfection under fluorescence microscopy (GFP filter).
Protocol (PDF):
FP318
MSDS (PDF):
MSDS-FP318
MSDS-FP319
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