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CRISPR-Lenti Non-Targeting Control Transduction Particles

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Quality Level


vial of 200 μL


1x106  VP/ml (via p24 assay)



shipped in

dry ice

storage temp.


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General description

The Sigma lenti CRISPR Non-Targeting Control is a lentiviral system, which includes a gRNA sequence that does not target known human, mouse and rat genes. The non-targeting control lentivirus is useful as a negative control in experiments using Sigma CRISPR lentiviral clones. The Sigma lenti CRISPR non-targeting control uses a one-plasmid system consisting of a EF1-alpha-driven Cas9, a U6-driven guide RNA (non-targeting), with both Puromycin and GFP co-expressed with Cas9.

Ampicillin and puromycin antibiotic resistance genes provide selection in bacterial or mammalian cells, respectively. Also, self-inactivating replication incompetent viral particles can be produced in packaging cells (HEK293T) by co-transfection with compatible packaging plasmids (Product No. SHP001).


CRISPR-Lenti Non-Targeting Control Transduction Particles has been used in the transduction of human embryonic kidney 293 luciferase expressing cells with lentiviral particles, isolation of single colonies and MOSPD2 (motile sperm domain containing protein 2) silencing.
Functional Genomics/Screening/Target Validation
  • Non-targeting control, CRISPR lentivirus, viral format, for creating gene knockouts/genetic modifications in cell lines.

To see more application data, protocols, vector maps visit

Features and Benefits

Serves as a non-targeting or negative experimental control (lentiviral format) for the CRISPR editing workflow using lenti CRISPRs. This allows you to examine the effect of transduction in your system with the Sigma lenti CRISPR/Cas9 virus.

Physical form

200 μl of 106 TU/ml (via p24 titering assay) lentiviral particles are provided as frozen stock.

Storage Class Code

12 - Non Combustible Liquids



Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Newly characterized motile sperm domain-containing protein 2 promotes human breast cancer metastasis.
Salem Y, et al.
International Journal of Cancer. Journal International Du Cancer, 1-33 null
Knocking out Ornithine Decarboxylase Antizyme 1 (OAZ1) Improves Recombinant Protein Expression in the HEK293 Cell Line.
Abaandou L and Shiloach J
Medecine Sciences : M/S, 6(2), 48-48 (2018)
Tina Dahlby et al.
International journal of molecular sciences, 21(21) (2020-11-04)
Selective inhibition of histone deacetylase 3 (HDAC3) prevents glucolipotoxicity-induced β-cell dysfunction and apoptosis by alleviation of proapoptotic endoplasmic reticulum (ER) stress-signaling, but the precise molecular mechanisms of alleviation are unexplored. By unbiased microarray analysis of the β-cell gene expression profile
Jennifer Maning et al.
International journal of molecular sciences, 21(8) (2020-04-25)
Aldosterone (Aldo), when overproduced, is a cardiotoxic hormone underlying heart failure and hypertension. Aldo exerts damaging effects via the mineralocorticoid receptor (MR) but also activates the antiapoptotic G protein-coupled estrogen receptor (GPER) in the heart. G protein-coupled receptor (GPCR)-kinase (GRK)-2


CRISPR Cas 9 Nuclease RNA-guided Genome Editing

Learn about CRISPR Cas9, what it is and how it works. CRISPR is a new, affordable genome editing tool enabling access to genome editing for all.

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