pSUPER.retro.puro

shRNA gene silencing Rat - MM1 SSH2

Experiment
shRNA gene silencing Rat - MM1 SSH2
Product
pSUPER.retro.puro from Oligoengine
Manufacturer
Oligoengine

Protocol tips

Upstream tips
5′-TGCGTCAAACTTAGAGGAC-3′
Protocol tips
The plasmids for retroviral expression were constructed by subcloning the cDNAs encoding cyan fluorescent protein (CFP), or CFP-tagged human SSH1 (CFP-hSSH1), mouse SSH2 (mSSH2-CFP), human wild-type (WT) LIMK1 (hLIMK1(WT)-CFP), or human kinase-dead LIMK1 (hLIMK1(D460A)-CFP) (30), or Myc-tagged chick cofilin (ch-cofilin) or ADF (ch-ADF), into the pLNCX-neo retroviral vector (Clontech, Palo Alto, CA). The siRNA-targeting constructs were generated using the pSUPER.retro.puro vector (Oligo-Engine, Seattle, WA), as described previously (32). The 19-base targeting sequences used in this study were as follows: 5′-GAACTGTCGACCAAGAAAG-3′ (rat SSH1), 5′-TGCGTCAAACTTAGAGGAC-3′ (rat SSH2), 5′-GCTGGAACAATGGCTAGAA-3′ (rat LIMK1), 5′-GCACGAATTACAAGCTAAC-3′ (rat cofilin), and 5′-GCACGAGTATCAAGCAAAT-3′ (rat ADF). As a control, we used a nontargeting sequence, 5′-TCTTCCCCCAAGAAAGATA-3′, which does not exist in the rat genome.To generate retroviral supernatants, Plat-E retrovirus packaging cells (33) were transfected with pLNCX-neo or pSUPER.retro.puro plasmids using FuGENE6 (Roche Applied Science, Mannheim, Germany). At 48 h after transfection, the culture medium was centrifuged, and the viral supernatant was used for infection after the addition of 8 μg/ml polybrene. Infected MM1 cells were cultured for 24 h, washed, and selected by culturing for 48 h with 2 μg/ml puromycin for cells infected with pSUPER.retro.puro retrovirus or for 2 weeks with 250 μg/ml G418 (Nacalai Tesque, Kyoto, Japan) for cells infected with pLNCX retrovirus.

Publication protocol

The plasmids for retroviral expression were constructed by subcloning the cDNAs encoding cyan fluorescent protein (CFP), or CFP-tagged human SSH1 (CFP-hSSH1), mouse SSH2 (mSSH2-CFP), human wild-type (WT) LIMK1 (hLIMK1(WT)-CFP), or human kinase-dead LIMK1 (hLIMK1(D460A)-CFP) (30), or Myc-tagged chick cofilin (ch-cofilin) or ADF (ch-ADF), into the pLNCX-neo retroviral vector (Clontech, Palo Alto, CA). The siRNA-targeting constructs were generated using the pSUPER.retro.puro vector (Oligo-Engine, Seattle, WA), as described previously (32). The 19-base targeting sequences used in this study were as follows: 5′-GAACTGTCGACCAAGAAAG-3′ (rat SSH1), 5′-TGCGTCAAACTTAGAGGAC-3′ (rat SSH2), 5′-GCTGGAACAATGGCTAGAA-3′ (rat LIMK1), 5′-GCACGAATTACAAGCTAAC-3′ (rat cofilin), and 5′-GCACGAGTATCAAGCAAAT-3′ (rat ADF). As a control, we used a nontargeting sequence, 5′-TCTTCCCCCAAGAAAGATA-3′, which does not exist in the rat genome.To generate retroviral supernatants, Plat-E retrovirus packaging cells (33) were transfected with pLNCX-neo or pSUPER.retro.puro plasmids using FuGENE6 (Roche Applied Science, Mannheim, Germany). At 48 h after transfection, the culture medium was centrifuged, and the viral supernatant was used for infection after the addition of 8 μg/ml polybrene. Infected MM1 cells were cultured for 24 h, washed, and selected by culturing for 48 h with 2 μg/ml puromycin for cells infected with pSUPER.retro.puro retrovirus or for 2 weeks with 250 μg/ml G418 (Nacalai Tesque, Kyoto, Japan) for cells infected with pLNCX retrovirus.

Full paper   Login or join for free to view the full paper.

Reviews

pSUPER.retro.puro from Oligoengine has not yet been reviewed for this experiment

We'd love it if you would be the first to write a review!

Discussion

Start your discussion

Share your thoughts or question with experts in your field

Start a discussion

Papers

Check out relevant papers found by Labettor's AI that are relevant for performing shRNA gene silencing Rat - MM1 SSH2 using pSUPER.retro.puro from Oligoengine.

View full paper   Login or join for free to view the full paper.

Manufacturer protocol

Download the product protocol from Oligoengine for pSUPER.retro.puro below.

Download PDF Download manufacturer protocol

Videos

Check out videos that might be relevant for performing shRNA gene silencing Rat - MM1 SSH2 using pSUPER.retro.puro from Oligoengine. Please note that these videos are representative and steps or experiment specific processes must be kept in mind to expect desired results.

We haven't found any additional videos for this experiment / product combination yet.

Outsource your experiment

Fill out your contact details and receive price quotes in your Inbox

  Outsource experiment
Become shareholder Discussions About us Contact Privacy Terms