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Addgene inc m ay 3
M Ay 3, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/m+ay+3/pLKO-puro+human+lipin+1-1+shRNA+(Plasmid+%2332019)/pm31043460-89-37-106
Average 91 stars, based on 3 article reviews
m ay 3 - by Bioz Stars, 2026-10
91/100 stars

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Related Articles

Sequencing:

Article Title: Identification of MRP4/ABCC4 as a Target for Reducing the Proliferation of Pancreatic Ductal Adenocarcinoma Cells by Modulating the cAMP Efflux.
Article Snippet: Oligonucleotides were cloned into the pSUPER.retro.puro vector (OligoEngine); their correct orientation after cloning was confirmed by DNA sequencing using the following primer: 5 ́-GGAAGCCTTGGCTTTTG-3 ́ (Macrogen). .. MRP4-shRNA oligonucleotides contained a MRP4 mRNA specific region, a hairpin loop region (bold), and a linker sequence for subcloning into the pSUPER vector (italic): MRP4-shRNA1 sequence (5 ́-3 ́) sense:GATCCCCCAGTGTTCTTACACTTCCTTTCAAGAGAAGGAAGTGTAAGAACACT GTTTTTA antisense:AGCTTAAAAACAGTGTTCTTACACTTCCTTCTCTTGAAAGGAAGTGTAAGAA CACTGGGG at A SPE T Journals on M ay 3, 2019 m olpharm .aspetjournals.org D ow nloaded from MOL # 115444 13 MRP4-shRNA2 sequence (5 ́-3 ́) sense:GATCCCCGATGGTGCATGTGCAGGATTTCAAGAGAATCCTGCACATGCAGCAT CTTTTTA antisense:AGCTTAAAAAGATGGTGCATGTGCAGGATTCTCTTGAAATCCTGCACATGC AGCATCGGG scramble-shRNA sequence (5 ́-3 ́) sense:GATCCCCGAAACTGCTGACCGTTAATTTCAAGAGAATTAACGGTCAGCAGTTT CTTTTTA antisense:AGCTTAAAAAGAAACTGCTGACCGTTAATTCTCTTGAAATTAACGGTCAGCA GTTTCGGG Stable PANC-1 cells expressing shRNA targeting MRP4 Retroviruses were generated in HEK293T cells seeded in a 10cm plate one day prior to calcium phosphate-mediated co-transfection with either a sequence of pSUPER-MRP4shRNA or pSUPER-scramble-shRNA in combination with viral packaging expression plasmids (Addgene). ..

Subcloning:

Article Title: Identification of MRP4/ABCC4 as a Target for Reducing the Proliferation of Pancreatic Ductal Adenocarcinoma Cells by Modulating the cAMP Efflux.
Article Snippet: Oligonucleotides were cloned into the pSUPER.retro.puro vector (OligoEngine); their correct orientation after cloning was confirmed by DNA sequencing using the following primer: 5 ́-GGAAGCCTTGGCTTTTG-3 ́ (Macrogen). .. MRP4-shRNA oligonucleotides contained a MRP4 mRNA specific region, a hairpin loop region (bold), and a linker sequence for subcloning into the pSUPER vector (italic): MRP4-shRNA1 sequence (5 ́-3 ́) sense:GATCCCCCAGTGTTCTTACACTTCCTTTCAAGAGAAGGAAGTGTAAGAACACT GTTTTTA antisense:AGCTTAAAAACAGTGTTCTTACACTTCCTTCTCTTGAAAGGAAGTGTAAGAA CACTGGGG at A SPE T Journals on M ay 3, 2019 m olpharm .aspetjournals.org D ow nloaded from MOL # 115444 13 MRP4-shRNA2 sequence (5 ́-3 ́) sense:GATCCCCGATGGTGCATGTGCAGGATTTCAAGAGAATCCTGCACATGCAGCAT CTTTTTA antisense:AGCTTAAAAAGATGGTGCATGTGCAGGATTCTCTTGAAATCCTGCACATGC AGCATCGGG scramble-shRNA sequence (5 ́-3 ́) sense:GATCCCCGAAACTGCTGACCGTTAATTTCAAGAGAATTAACGGTCAGCAGTTT CTTTTTA antisense:AGCTTAAAAAGAAACTGCTGACCGTTAATTCTCTTGAAATTAACGGTCAGCA GTTTCGGG Stable PANC-1 cells expressing shRNA targeting MRP4 Retroviruses were generated in HEK293T cells seeded in a 10cm plate one day prior to calcium phosphate-mediated co-transfection with either a sequence of pSUPER-MRP4shRNA or pSUPER-scramble-shRNA in combination with viral packaging expression plasmids (Addgene). ..

Plasmid Preparation:

Article Title: Identification of MRP4/ABCC4 as a Target for Reducing the Proliferation of Pancreatic Ductal Adenocarcinoma Cells by Modulating the cAMP Efflux.
Article Snippet: Oligonucleotides were cloned into the pSUPER.retro.puro vector (OligoEngine); their correct orientation after cloning was confirmed by DNA sequencing using the following primer: 5 ́-GGAAGCCTTGGCTTTTG-3 ́ (Macrogen). .. MRP4-shRNA oligonucleotides contained a MRP4 mRNA specific region, a hairpin loop region (bold), and a linker sequence for subcloning into the pSUPER vector (italic): MRP4-shRNA1 sequence (5 ́-3 ́) sense:GATCCCCCAGTGTTCTTACACTTCCTTTCAAGAGAAGGAAGTGTAAGAACACT GTTTTTA antisense:AGCTTAAAAACAGTGTTCTTACACTTCCTTCTCTTGAAAGGAAGTGTAAGAA CACTGGGG at A SPE T Journals on M ay 3, 2019 m olpharm .aspetjournals.org D ow nloaded from MOL # 115444 13 MRP4-shRNA2 sequence (5 ́-3 ́) sense:GATCCCCGATGGTGCATGTGCAGGATTTCAAGAGAATCCTGCACATGCAGCAT CTTTTTA antisense:AGCTTAAAAAGATGGTGCATGTGCAGGATTCTCTTGAAATCCTGCACATGC AGCATCGGG scramble-shRNA sequence (5 ́-3 ́) sense:GATCCCCGAAACTGCTGACCGTTAATTTCAAGAGAATTAACGGTCAGCAGTTT CTTTTTA antisense:AGCTTAAAAAGAAACTGCTGACCGTTAATTCTCTTGAAATTAACGGTCAGCA GTTTCGGG Stable PANC-1 cells expressing shRNA targeting MRP4 Retroviruses were generated in HEK293T cells seeded in a 10cm plate one day prior to calcium phosphate-mediated co-transfection with either a sequence of pSUPER-MRP4shRNA or pSUPER-scramble-shRNA in combination with viral packaging expression plasmids (Addgene). ..

Expressing:

Article Title: Identification of MRP4/ABCC4 as a Target for Reducing the Proliferation of Pancreatic Ductal Adenocarcinoma Cells by Modulating the cAMP Efflux.
Article Snippet: Oligonucleotides were cloned into the pSUPER.retro.puro vector (OligoEngine); their correct orientation after cloning was confirmed by DNA sequencing using the following primer: 5 ́-GGAAGCCTTGGCTTTTG-3 ́ (Macrogen). .. MRP4-shRNA oligonucleotides contained a MRP4 mRNA specific region, a hairpin loop region (bold), and a linker sequence for subcloning into the pSUPER vector (italic): MRP4-shRNA1 sequence (5 ́-3 ́) sense:GATCCCCCAGTGTTCTTACACTTCCTTTCAAGAGAAGGAAGTGTAAGAACACT GTTTTTA antisense:AGCTTAAAAACAGTGTTCTTACACTTCCTTCTCTTGAAAGGAAGTGTAAGAA CACTGGGG at A SPE T Journals on M ay 3, 2019 m olpharm .aspetjournals.org D ow nloaded from MOL # 115444 13 MRP4-shRNA2 sequence (5 ́-3 ́) sense:GATCCCCGATGGTGCATGTGCAGGATTTCAAGAGAATCCTGCACATGCAGCAT CTTTTTA antisense:AGCTTAAAAAGATGGTGCATGTGCAGGATTCTCTTGAAATCCTGCACATGC AGCATCGGG scramble-shRNA sequence (5 ́-3 ́) sense:GATCCCCGAAACTGCTGACCGTTAATTTCAAGAGAATTAACGGTCAGCAGTTT CTTTTTA antisense:AGCTTAAAAAGAAACTGCTGACCGTTAATTCTCTTGAAATTAACGGTCAGCA GTTTCGGG Stable PANC-1 cells expressing shRNA targeting MRP4 Retroviruses were generated in HEK293T cells seeded in a 10cm plate one day prior to calcium phosphate-mediated co-transfection with either a sequence of pSUPER-MRP4shRNA or pSUPER-scramble-shRNA in combination with viral packaging expression plasmids (Addgene). ..

shRNA:

Article Title: Identification of MRP4/ABCC4 as a Target for Reducing the Proliferation of Pancreatic Ductal Adenocarcinoma Cells by Modulating the cAMP Efflux.
Article Snippet: Oligonucleotides were cloned into the pSUPER.retro.puro vector (OligoEngine); their correct orientation after cloning was confirmed by DNA sequencing using the following primer: 5 ́-GGAAGCCTTGGCTTTTG-3 ́ (Macrogen). .. MRP4-shRNA oligonucleotides contained a MRP4 mRNA specific region, a hairpin loop region (bold), and a linker sequence for subcloning into the pSUPER vector (italic): MRP4-shRNA1 sequence (5 ́-3 ́) sense:GATCCCCCAGTGTTCTTACACTTCCTTTCAAGAGAAGGAAGTGTAAGAACACT GTTTTTA antisense:AGCTTAAAAACAGTGTTCTTACACTTCCTTCTCTTGAAAGGAAGTGTAAGAA CACTGGGG at A SPE T Journals on M ay 3, 2019 m olpharm .aspetjournals.org D ow nloaded from MOL # 115444 13 MRP4-shRNA2 sequence (5 ́-3 ́) sense:GATCCCCGATGGTGCATGTGCAGGATTTCAAGAGAATCCTGCACATGCAGCAT CTTTTTA antisense:AGCTTAAAAAGATGGTGCATGTGCAGGATTCTCTTGAAATCCTGCACATGC AGCATCGGG scramble-shRNA sequence (5 ́-3 ́) sense:GATCCCCGAAACTGCTGACCGTTAATTTCAAGAGAATTAACGGTCAGCAGTTT CTTTTTA antisense:AGCTTAAAAAGAAACTGCTGACCGTTAATTCTCTTGAAATTAACGGTCAGCA GTTTCGGG Stable PANC-1 cells expressing shRNA targeting MRP4 Retroviruses were generated in HEK293T cells seeded in a 10cm plate one day prior to calcium phosphate-mediated co-transfection with either a sequence of pSUPER-MRP4shRNA or pSUPER-scramble-shRNA in combination with viral packaging expression plasmids (Addgene). ..

Generated:

Article Title: Identification of MRP4/ABCC4 as a Target for Reducing the Proliferation of Pancreatic Ductal Adenocarcinoma Cells by Modulating the cAMP Efflux.
Article Snippet: Oligonucleotides were cloned into the pSUPER.retro.puro vector (OligoEngine); their correct orientation after cloning was confirmed by DNA sequencing using the following primer: 5 ́-GGAAGCCTTGGCTTTTG-3 ́ (Macrogen). .. MRP4-shRNA oligonucleotides contained a MRP4 mRNA specific region, a hairpin loop region (bold), and a linker sequence for subcloning into the pSUPER vector (italic): MRP4-shRNA1 sequence (5 ́-3 ́) sense:GATCCCCCAGTGTTCTTACACTTCCTTTCAAGAGAAGGAAGTGTAAGAACACT GTTTTTA antisense:AGCTTAAAAACAGTGTTCTTACACTTCCTTCTCTTGAAAGGAAGTGTAAGAA CACTGGGG at A SPE T Journals on M ay 3, 2019 m olpharm .aspetjournals.org D ow nloaded from MOL # 115444 13 MRP4-shRNA2 sequence (5 ́-3 ́) sense:GATCCCCGATGGTGCATGTGCAGGATTTCAAGAGAATCCTGCACATGCAGCAT CTTTTTA antisense:AGCTTAAAAAGATGGTGCATGTGCAGGATTCTCTTGAAATCCTGCACATGC AGCATCGGG scramble-shRNA sequence (5 ́-3 ́) sense:GATCCCCGAAACTGCTGACCGTTAATTTCAAGAGAATTAACGGTCAGCAGTTT CTTTTTA antisense:AGCTTAAAAAGAAACTGCTGACCGTTAATTCTCTTGAAATTAACGGTCAGCA GTTTCGGG Stable PANC-1 cells expressing shRNA targeting MRP4 Retroviruses were generated in HEK293T cells seeded in a 10cm plate one day prior to calcium phosphate-mediated co-transfection with either a sequence of pSUPER-MRP4shRNA or pSUPER-scramble-shRNA in combination with viral packaging expression plasmids (Addgene). ..



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