UserName
Generate RNA transcripts with higher protein yields
Quickly cleanup large-scale transcription reactions
in vitro synthesis of large amounts of capped RNA
Maximize the yield of short RNA transcripts
Generate RNA transcripts with higher protein yields
Versatile transfection reagent that has been shown to effectively transfect the widest variety of adherent and suspension cell lines
in vitro synthesis of large amounts of capped RNA
Obtain 10–50 times yield of conventional in vitro transcription reactions
The MegaScript T7 Transcription Kit Plus contains all the reagents and buffers necessary for in vitro synthesis of large amounts of RNA.
Format | Kit |
---|---|
Final Product Type | In vitro Transcribed RNA |
Sample Type | In vitro Transcribed RNA,Total RNA |
Isolation Technology | Silica Spin Column |
Purification Target | In vitro Transcribed RNA |
Cell Type | HEK293,293,HeLa,CHO-K1,CHO,Jurkat,Primary Human T Cells,Primary Cells,Stem Cells,iPSC,NIH-3T3,HepG2,A549,HUVEC |
The mMESSAGE mMACHINE T7 mRNA Kit with CleanCap Reagent AG contains all the reagents and buffers necessary for in vitro synthesis of large amounts of mRNA with the naturally occurring Cap 1 structure.
Format | Kit |
---|---|
Final Product Type | Synthetic mRNA,mRNA |
Sample Type | mRNA,Synthetic mRNA |
Isolation Technology | Silica Spin Column |
Purification Target | mRNA,Synthetic mRNA |
Cell Type | HEK293,293,HeLa,CHO-K1,CHO,Jurkat,Primary Human T Cells,Primary Cells,Stem Cells,iPSC,NIH-3T3,HepG2,A549,HUVEC |
The CytoTune™-iPS 2.0 Sendai Reprogramming Kit improves upon the well-referenced CytoTune™-iPS Sendai Reprogramming Kit.
Shipping Condition | Dry Ice |
---|---|
Promoter | Proprietary |
Format | Kit |
Sub Cellular Localization | Cytoplasm |
Product Type | Sendai Reprogramming Kit |
Delivery Type | Sendai virus |
For Use With (Application) | Stem Cell Engineering & Reprogramming |
Product Line | CytoTune™ |
The first off-the-shelf reprogramming system designed for clinical and translational research
For 5' capped RNA molecule synthesis as part of in vitro transcription reactions