Hieff Trans™ Booster DNA/RNA Transfection Reagent (Lipo3000 alternative) _ 40801ES yeasen

$75.00
In stock
SKU
40801ES01
Catalog No.SizePrice (USD)
40801ES01100 μL$75.00
40801ES030.75mL$355.00
40801ES041.5 mL$645.00

Product Description

Booster DNA/RNA Transfection Reagent is an advanced nucleic acid transfection reagent developed based on novel polymeric materials. Its unique molecular design significantly reduces cytotoxicity and features a smart anti-enzymatic degradation mechanism that protects nucleic acids from intracellular enzymatic degradation during delivery, thereby maximizing transfection efficiency. This reagent is suitable for various types of nucleic acids including DNA, siRNA, miRNA, mRNA, and ASO, and has been validated for efficient transfection in cell lines such as 293T, HeLa, MCF7, HepG2, A549, NIH3T3, RAW264.7, HCT116, as well as primary cells, providing reliable tools for gene research. Unique Mechanism Enhances Transfection Efficiency at Every Step. Hieff Trans™ Booster is a next-generation polymeric transfection reagent. By utilizing a novel polymeric formulation—identified through our AI-integrated high-throughput screening, it achieves significantly higher delivery efficiency in challenging models—such as primary neurons, T-cells, and suspension cells—while ensuring exceptional cell viability. Its unique mechanism enhances transfection efficiency at every step, delivering higher success rates for your transfection experiments!

1) High Loading Capacity → Dual mechanism: charge interaction + polymer chain entanglement; Higher loading capacity than traditional charge-interaction methods. 2) Efficient Cellular Uptake → Membrane translocation; Faster than conventional endocytosis pathways. 3) Non-Damaging Release → Rapid polymer degradation by intracellular enzymes/reducing GSH; Zero-damage release of nucleic acids. 4) Enhanced Safety → Rapid polymer degradation property; Lower toxicity than traditional lipid-based transfection reagents.

Features

  • s
  • L
  • ow
  • C
  • ytotoxicity
  • The novel
  • p
  • olymer replaces traditional liposomes to reduce cytotoxicity and improve
  • cell
  • viability
  • Fast Release and
  • Higher Efficiency
  • Fast
  • release minimizes intracellular nucleic acid degradation, achieving >90% tra
  • nsfection efficiency (measured by flow cytometry).
  • P
  • remium Options for
  • Difficult-to-transfect cell lines
  • : S
  • ensitive and primary cells.
  • Proven Performance, Broad Cell Line Coverage:
  • Achieves high efficiency in
  • 200+ various
  • cell lines including 293T, HeLa, MCF7, HepG2, A549, NIH3T3, RAW264.7, and HCT116 and primary cells, with consistent and reproducible results
  • One Reagent
  • All Nucleic Acids
  • Delivers DNA, siRNA, miRNA, mRNA, and ASO with high efficiency—even up to 15 kb fragments.

Components

  • No.
  • Name
  • 40801
  • ES
  • 01
  • 40801
  • ES
  • 03
  • 40801
  • ES
  • 04
  • 40801-A
  • Booster
  • DNA/RNA Tran
  • sfection
  • Reagent
  • 100
  • μL
  • 0.75
  • mL
  • 1.5
  • mL
  • 40801-B
  • Transfection Enhancer
  • 100
  • μL
  • 0.75
  • mL
  • 1.5
  • mL

Shipping and Storage

This product should be stor ed at 2~8℃ for 12 months.

Applications

  • Cell Transfection; DNA Transfection; mRNA/siRNA Transfection;

Figures

1) High-Efficiency DNA Transfection

Figure 1 DNA transfection across different cells using Booster DNA&RNA Transfection Reagent versus L *3000 . The result d emonstrates superior DNA transfection efficiency of Booster 2) High-Efficiency mRNA Transfection

Figure 2 mRNA transfection across different cells using Booster DNA&RNA Transfection Reagent versus L *3000 . The result d emonstrates superior mRNA transfection efficiency of Booster 3) High-Efficiency siRNA Transfection

Figure 3 siRNA transfection across different cells using Booster DNA&RNA Transfection Reagent versus L *3000 . The result d emonstrates superior siRNA transfection efficiency of Booster Customer Feedback 1) High-Efficiency Primary Dermal Fibroblasts Transfection

Figure 4 Plasmid EGFR DNA transfection in primary dermal fibroblasts using Booster DNA&RNA Transfection Reagent versus L * 3000 . The result d emonstrates superior primary cell transfection efficiency of Booster 2) High-Efficiency Porcine Alveolar Macrophages Transfection

Figure 5 DNA transfection in primary Porcine Alveolar Macrophages (PAMs) using Booster DNA&RNA Transfection Reagent versus L * 3000. The result d emonstrates superior primary cell transfection efficiency of Booster

Documents

  • More Customer Cases
  • -English Version
  • More Customer Cases-Korean Version
  • More Customer Cases-Japanese Version

Safety Data Sheet

  • 40801_MSDS_HB250715_EN.PDF

Manuals

Reviews

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