Scramble control hairpin in pCDH-CMV-MCS-EF1-copGFP (CD511B-1)

No need to make a negative control for your Human Precursor miRNA Expression Lentivector Studies—SBI’s already built one for you. With the Human pre-miRNA Scramble Negative Control Expression Lentivector, you get the same lentivector that expresses our targeted miRNAs, but with a scrambled, non-targeting stem-loop sequence so you can easily control for increased miRNA effects.

The Human pre-miRNA Scramble Negative Control Expression Lentivector is available as both ready-to-transfect lentivector plasmid and ready-to-transduce pre-packaged lentivirus.

Whether you’re using miRNAs to study cellular processes or develop the next generation of therapeutics, SBI’s comprehensive collection of Lenti-miRs™—human precursor miRNA lentivectors—are a superior alternative to synthetic RNAs. Like synthetic miRs, SBI’s Lenti-miRs can be transfected into target cells for transient miR expression. But unlike synthetic miRs, they can also be transduced into a variety of target cells—including primary cells, stem cells, and other hard-to-transfect cell lines—to create stable miR-producing cell lines, maximizing your options for miR expression.

In addition, SBI’s precursor miRNA lentivectors are designed for efficient expression and accurate processing into mature miRNAs, for native miR-like behavior. Each construct is cloned with the native stem-loop structure plus an additional 200 – 400 bps of upstream and downstream DNA, ensuring that the miRNA processing machinery operates just as it would with the native transcript.

And because our collection includes cancer and stem cell-related miRNA clusters, we offer a wider range of constructs than just the mature miRNA sequences listed in miRbase.

The precursor miRNA Expression Lentivectors drive expression of the miR precursor with the constitutive CMV promoter, for strong expression in common cell types including HeLa, HEK293, and HT1080 cell lines. Transductants/transfectants can be easily sorted using copGFP.

• Transfect or transduce the precursor miRNA lentivectors
• Create stably-expressing miR cell lines
• Leverage SBI’s highly-regarded lentivectors
• Obtain accurate miR processing and efficient expression through the use of native precursor sequences
• Use copGFP markers to identify desired clones