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Home > Gene Editing and Analysis > Transfection > Trasfection Overview
Transfection
  • Trasfection Overview
  • Antibiotic Selection, Expression vectors and FBS
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Trasfection Overview

TaKaRa Bio

Introduce the specific genetic material into eukaryotic cell by various methods of transfection

Trasfection Overview
TaKaRa Bio

Except of lentiviral, retroviral and adenoviral gene delivery systems TaKaRa Bio offers the huge portfolio of transfection reagent products and also the other tools using with transfection as serums, antibiotic markers, plasmids and others.

 

Xfect Trasfection Reagent 

  • For plasmid transfection which is suitable for most of the cells
  • The reagent is made by biodegradable transfection polymer
  • Has high transfection efficiency and very low cytotoxicity profile

 

Mouse Embryonic Stem Cell Transfection Reagent

  • Special type of reagent offers the superior gene expression in these types of cells

 

Calcium Phosphate Reagent

  • Suitable for home brew calcium phosphate buffers due to its consistent pH and salt concentration

 

RNA Transfection Reagent

  • Optimized for all RNA transfection with all types of RNA including siRNA, miRNA, mRNA
  • Also suitable for sgRNA for CRISPR/Cas9 mediated gene editing

 

Protein Transfection Reagent

  • Extremely rapid Reagent
  • Suitable for studies of transient effects of proteins
  • It also eliminates the possibility of random DNA integration into target cells genomes.

 

Xfect Single Shots

  • Simplify the transfection into one step

 

Documents and resources

For more information visit producer's website.

Transfection Reagent Products

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Cloning Enhancer

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Cloning Enhancer removes background of PCR products without purification

Lentiviral Transduction

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Lentiviral gene delivery allows the introduction and expression of a gene of interest in mammalian cells

Adenoviral Transduction

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Adenoviral gene delivery allows the introduction and expression of a gene of interest in mammalian cells

Viral Delivery of sgRNA/Cas9

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The Cas9/sgRNA can be delivered into the target cells by AAV and lentiviral systems

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