|Cloning||CRISPR/Lentiviral Library Construction||Phage Display|
|E. cloni® 10G ElectroComp |
>2 × 1010 cfu/µg transformation efficiency for cloning, subcloning, and plasmid isolation with or without blue/white screening. Superior substitute for cells such as DH10B, JM109.
|Endura™ ElectroComp |
>1 × 1010 cfu/µg transformation efficiency for stability of clones with repeated sequences such as lentiviral vectors. Recommended for GeCKO CRISPR library transformation.
|Phage Display ElectroCombo Pack |
>2-4 × 1010 cfu/µg transformation efficiency for phage display (electrocompetent cells). Four transformations of three strains [TG1, SS320 (MC1061 F'), ER2738]. Determine which strain performs best for your library construction.
E. cloni 10G ChemComp
|Endura ChemComp |
>1 × 108 cfu/µg transformation efficiency for stability of clones with repeated sequences such as lentiviral vectors. 2 transformations per tube.
|TransforMax™ EPI300™ ElectroComp |
>1 × 1010 cfu/µg transformation efficiency for high efficiency Gibson Assembly® and large-insert cloning, along with plasmid copy number control of CopyControl™ vectors.
*Available in US, Canada, and other select countries. Contact Lucigen customer service for any questions.