antisense oligo Search Results


antisense oligonucleotides  (Integrated DNA Technologies)
94
Integrated DNA Technologies antisense oligonucleotides
Antisense Oligonucleotides, supplied by Integrated DNA Technologies, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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antisense oligonucleotides  (Oligos Etc)
90
Oligos Etc antisense oligonucleotides
Antisense Oligonucleotides, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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smyd1a -specific antisense morpholino oligos e9i9-mo  (Oligos Etc)
90
Oligos Etc smyd1a -specific antisense morpholino oligos e9i9-mo
Smyd1a Specific Antisense Morpholino Oligos E9i9 Mo, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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antisense phosphorothioate-substituted oligodeoxynucleotide 59-ggaccggtgcacttctcccca-39  (Oligos Etc)
90
Oligos Etc antisense phosphorothioate-substituted oligodeoxynucleotide 59-ggaccggtgcacttctcccca-39
Antisense Phosphorothioate Substituted Oligodeoxynucleotide 59 Ggaccggtgcacttctcccca 39, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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gdf-9 antisense oligos  (Oligos Etc)
90
Oligos Etc gdf-9 antisense oligos
Gdf 9 Antisense Oligos, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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p27 kip1 sirna  (Oligos Etc)
90
Oligos Etc p27 kip1 sirna
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
P27 Kip1 Sirna, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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biotinylated antisense oligonucleotides as-oligos  (Oligos Etc)
90
Oligos Etc biotinylated antisense oligonucleotides as-oligos
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
Biotinylated Antisense Oligonucleotides As Oligos, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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ezrin antisense vivo-morpholino oligo  (Gene Tools Inc)
90
Gene Tools Inc ezrin antisense vivo-morpholino oligo
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
Ezrin Antisense Vivo Morpholino Oligo, supplied by Gene Tools Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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antisense oligo- nts (asos) to deplete snora73b (tgatg tac agt ccc tttcca)  (Ribobio co)
90
Ribobio co antisense oligo- nts (asos) to deplete snora73b (tgatg tac agt ccc tttcca)
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
Antisense Oligo Nts (Asos) To Deplete Snora73b (Tgatg Tac Agt Ccc Tttcca), supplied by Ribobio co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antisense oligo- nts (asos) to deplete snora73b (tgatg tac agt ccc tttcca)/product/Ribobio co
Average 90 stars, based on 1 article reviews
antisense oligo- nts (asos) to deplete snora73b (tgatg tac agt ccc tttcca) - by Bioz Stars, 2026-04
90/100 stars
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aumsilencetm fana antisense  (Oligos Etc)
90
Oligos Etc aumsilencetm fana antisense
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
Aumsilencetm Fana Antisense, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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antisense dna oligo probes  (LGC Biosearch)
90
LGC Biosearch antisense dna oligo probes
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
Antisense Dna Oligo Probes, supplied by LGC Biosearch, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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antisense oligos (asos) targeting ppp1r3b  (Oligos Etc)
90
Oligos Etc antisense oligos (asos) targeting ppp1r3b
Viability of HCT116 cell lines transfected with p21 WAF or <t>p27</t> <t>KIP1</t> siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 <t>siRNA-transfected</t> HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.
Antisense Oligos (Asos) Targeting Ppp1r3b, supplied by Oligos Etc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Image Search Results


Viability of HCT116 cell lines transfected with p21 WAF or p27 KIP1 siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 siRNA-transfected HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.

Journal: Cancer Gene Therapy

Article Title: RNA interference-mediated knockdown of p21 WAF1 enhances anti-tumor cell activity of oncolytic adenoviruses

doi: 10.1038/cgt.2009.29

Figure Lengend Snippet: Viability of HCT116 cell lines transfected with p21 WAF or p27 KIP1 siRNAs before adenovirus infection. HCT116-WT or HCT116 p53−/− were transfected with p21 WAF1 or p27 KIP1 siRNAs. Adenovirus infections were carried out 48 h later. For HCT116 cells, viability was assessed 72 h after addition of the wild-type adenovirus (WtD) or Delta-24 adenoviruses or 94 h for ONYX-015. For HCT116 p53−/− cells, viability was assessed 72 h after addition of the WtD or 94 h for ONYX-015 and Delta-24. Western blot analysis of p21 WAF1 ( a and c ) or p27 KIP1 ( b and d ) expression in HCT116-WT cells transfected with p21 WAF1 (oligos #11 and #12), p27 KIP1 (oligos #5 and #8), or non-targeting control siRNAs. β-actin was used as loading control. Cell viability of p21 WAF1 or p27 KIP1 siRNA-transfected HCT116-WT ( e – g ) or HCT116 p53−/− ( h – j ) cells followed by WtD ( e and h ), ONYX-015 ( f and i ) or Delta-24 ( g and j ) infection. Viability is expressed as a relative percentage of cells transfected with non-targeting siRNA control. Error bars indicate s.d. * P <0.05, ** P <0.005 compared with negative control.

Article Snippet: Only a reduction of the viability to 60% after Delta-24 was observed after transfection of p27 KIP1 siRNA (oligos #5 and #8) in HCT116 p53−/− cells.

Techniques: Transfection, Infection, Western Blot, Expressing, Control, Negative Control

Replication efficiency of adenovirus in HCT116-WT or HCT116 p53−/− cells transfected with p21 WAF1 or p27 KIP1 siRNAs. HCT116-WT ( a – c ) or HCT116 p53−/− ( d – f ) cells were transfected with p21 WAF1 or p27 KIP1 siRNAs for 48 h. The viral titers were determined 72 h after infection with wild-type adenovirus (WtD) ( a and d ) or ONYX-015 ( b and e ) or Delta-24 ( c and f ). Results are shown as means of duplicate experiments. Error bars represent s.d. * P <0.05, ** P <0.005 compared with negative control.

Journal: Cancer Gene Therapy

Article Title: RNA interference-mediated knockdown of p21 WAF1 enhances anti-tumor cell activity of oncolytic adenoviruses

doi: 10.1038/cgt.2009.29

Figure Lengend Snippet: Replication efficiency of adenovirus in HCT116-WT or HCT116 p53−/− cells transfected with p21 WAF1 or p27 KIP1 siRNAs. HCT116-WT ( a – c ) or HCT116 p53−/− ( d – f ) cells were transfected with p21 WAF1 or p27 KIP1 siRNAs for 48 h. The viral titers were determined 72 h after infection with wild-type adenovirus (WtD) ( a and d ) or ONYX-015 ( b and e ) or Delta-24 ( c and f ). Results are shown as means of duplicate experiments. Error bars represent s.d. * P <0.05, ** P <0.005 compared with negative control.

Article Snippet: Only a reduction of the viability to 60% after Delta-24 was observed after transfection of p27 KIP1 siRNA (oligos #5 and #8) in HCT116 p53−/− cells.

Techniques: Transfection, Infection, Negative Control

Viability of TE7 ( b ), H1299 ( c ), DU145 ( d ) and MIA PaCa-2 ( e ) cells transfected with p21 WAF1 siRNAs before adenovirus infections. Cells were transfected with p21 WAF1 siRNA for 48 h. Western blotting of p21 WAF1 ( a ) in cells transfected with p21 WAF1 siRNA or non-targeting siRNA. β-actin was used as loading control. Cell viability was measured at 72 h after infection with wild-type adenovirus (WtD), ONYX-015 or Delta-24. Data is represented as cell viability relative to untreated cells (equal to 100%). * P <0.05, ** P <0.005 compared with negative control.

Journal: Cancer Gene Therapy

Article Title: RNA interference-mediated knockdown of p21 WAF1 enhances anti-tumor cell activity of oncolytic adenoviruses

doi: 10.1038/cgt.2009.29

Figure Lengend Snippet: Viability of TE7 ( b ), H1299 ( c ), DU145 ( d ) and MIA PaCa-2 ( e ) cells transfected with p21 WAF1 siRNAs before adenovirus infections. Cells were transfected with p21 WAF1 siRNA for 48 h. Western blotting of p21 WAF1 ( a ) in cells transfected with p21 WAF1 siRNA or non-targeting siRNA. β-actin was used as loading control. Cell viability was measured at 72 h after infection with wild-type adenovirus (WtD), ONYX-015 or Delta-24. Data is represented as cell viability relative to untreated cells (equal to 100%). * P <0.05, ** P <0.005 compared with negative control.

Article Snippet: Only a reduction of the viability to 60% after Delta-24 was observed after transfection of p27 KIP1 siRNA (oligos #5 and #8) in HCT116 p53−/− cells.

Techniques: Transfection, Western Blot, Control, Infection, Negative Control

Replication efficiency of adenovirus in TE7, H1299, DU145 and MIA PaCa-2 cells transfected with p21 WAF1 siRNAs for 48 h. The viral titers were determined at 72 h after infection with wild-type adenovirus (WtD), ONYX-015 or Delta-24. Results are shown as means of duplicate experiments. Data are represented as relative percentage of cells transfected with non-targeting siRNA control (equal to 100%). Error bars represent s.d. ** P <0.005 compared with negative control.

Journal: Cancer Gene Therapy

Article Title: RNA interference-mediated knockdown of p21 WAF1 enhances anti-tumor cell activity of oncolytic adenoviruses

doi: 10.1038/cgt.2009.29

Figure Lengend Snippet: Replication efficiency of adenovirus in TE7, H1299, DU145 and MIA PaCa-2 cells transfected with p21 WAF1 siRNAs for 48 h. The viral titers were determined at 72 h after infection with wild-type adenovirus (WtD), ONYX-015 or Delta-24. Results are shown as means of duplicate experiments. Data are represented as relative percentage of cells transfected with non-targeting siRNA control (equal to 100%). Error bars represent s.d. ** P <0.005 compared with negative control.

Article Snippet: Only a reduction of the viability to 60% after Delta-24 was observed after transfection of p27 KIP1 siRNA (oligos #5 and #8) in HCT116 p53−/− cells.

Techniques: Transfection, Infection, Control, Negative Control