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CAS9HYGROV

Sigma-Aldrich

Cas9 Hygromycin Lentiviral Particles

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form

liquid

packaging

vial of 200 μL

concentration

≥1 x 10 6 VP/ml virus (via p24 assay)

application(s)

CRISPR

selection

blasticidin

shipped in

dry ice

storage temp.

−70°C

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LVCAS9NEO

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shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

storage temp.

−70°C

storage temp.

−70°C

storage temp.

−20°C

storage temp.

−70°C

form

liquid

form

liquid

form

liquid

form

-

packaging

vial of 200 μL

packaging

pkg of 8 x 25 μL (aliquots)

packaging

pkg of 8 x 25 μL (aliquots)

packaging

vial of 200 μL

application(s)

CRISPR

application(s)

CRISPR

application(s)

CRISPR

application(s)

CRISPR

General description

Ready-to-use Cas9-Hygro lentiviral particles enable immediate transduction of a wide range of cell lines. Cas9-Hygro lentiviral particles efficiently and stably integrate Cas9 and a hygromycin resistance cassette linked by a 2A peptide and driven by the EF1 alpha promoter (EF1a-Cas9-2A-Hygro) for strong expression in both dividing and non-dividing cell lines. They are ideal for avoiding the tedious lentivirus production process and are one part of a two part CRISPR system with individual Cas9 and gRNA expression vectors.

To order gRNA in any format click here

Application

Functional Genomics/Target Validation
  • Creation of gene knockouts in multiple cell lines
  • Complete knockout of genes not amenable to RNAi
  • Creation of cell lines stably expressing Cas9

Features and Benefits

  • Highly specific and highly active
  • Sequence verified
  • Ready to infect/transduce

Principle

CRISPR/Cas systems are employed by bacteria and archaea as a defense against invading viruses and plasmids. Recently, the type II CRISPR/Cas system from the bacterium Streptococcus pyogenes has been engineered to function in eukaryotic systems using two molecular components: a single Cas9 protein and a non-coding guide RNA (gRNA). The Cas9 endonuclease can be programmed with a single gRNA, directing a DNA double-strand break (DSB) at a desired genomic location. Similar to DSBs induced by zinc finger nucleases (ZFNs), the cell then activates endogenous DNA repair processes, either non-homologous end joining (NHEJ) or homology-directed repair (HDR), to heal the targeted DSB.

Unit Definition

VP/ml is the concentration unit of measure for viral titer estimated by p24 assay.

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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