noti-flanked minitransposon encoding the kanamycin resistance cassette m1-kan r (Thermo Fisher)
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noti-flanked minitransposon encoding the kanamycin resistance cassette m1-kan r
Noti Flanked Minitransposon Encoding The Kanamycin Resistance Cassette M1 Kan R, supplied by Thermo Fisher, 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/product/kan+r+cassette/noti+flanked+minitransposon+encoding+the+kanamycin+resistance+cassette+m1+kan+r/pmc06858789-478-3-13
Average 90 stars, based on 1 article reviews
Noti Flanked Minitransposon Encoding The Kanamycin Resistance Cassette M1 Kan R, supplied by Thermo Fisher, 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/product/kan+r+cassette/noti+flanked+minitransposon+encoding+the+kanamycin+resistance+cassette+m1+kan+r/pmc06858789-478-3-13
Average 90 stars, based on 1 article reviews
noti-flanked minitransposon encoding the kanamycin resistance cassette m1-kan r - by Bioz Stars,
2026-10
90/100 stars
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Isolation:Article Title: Stable Preanaphase Spindle Positioning Requires Bud6p and an Apparent Interaction between the Spindle Pole Bodies and the Neck Article Snippet: .. Transformants that had successfully integrated the cnm67 :: Polymerase Chain Reaction:Article Title: Stable Preanaphase Spindle Positioning Requires Bud6p and an Apparent Interaction between the Spindle Pole Bodies and the Neck Article Snippet: .. Transformants that had successfully integrated the cnm67 :: Article Title: A MultiSite Gateway Toolkit for Rapid Cloning of Vertebrate Expression Constructs with Diverse Research Applications Article Snippet: .. Unless otherwise stated, all 3’ entry vectors were generated by PCR amplification of the desired 3’ element using attB2R/B3-flanked oligonucleotide primers, followed by a BP reaction with pDONR P2R-P3 (Invitrogen). p3E-GFP-HA, p3E-YFP-HA (from pEYFP-C1, Clontech), p3E-CFP-HA (from pECFP-C1, Clontech), p3E-mCherry-HA (from p3E-mCherrypA [ ]), p3E-mKate2-HA and p3E-mKate2-myc no-polyadenylation signal (pA) were made by amplification of the coding sequences without a stop codon, but with the 3’ primer additionally containing an HA or c-myc epitope sequence followed by a stop codon. p3E-HA-Neuroligin1 was generated by amplification of HA-Neuroligin1 from a previously described vector [ ]. p3E-Dam-myc no-pA is from pNDam-Myc [ ]. p3E-SGTAP no-pA originated from pCeMM-CTAP(SG)-Gw [ ]. p3E-FRT-Kan R -FRT pA was cloned by amplifying the Transfection:Article Title: HVT-delivered chicken IGF-1 improves growth performance in broilers Article Snippet: .. The GS1783 cells harboring the pHVT-BAC-Kan-chIGF-1 was treated with l-arabinose at 32°C for 1 h followed by induction at 42°C to induce the I-SceI and remove the Cell Surface Hydrophobicity:Article Title: A Lambda-evo (λ evo ) phage platform for Zika virus E DIII protein display Article Snippet: .. Escherichia coli K-12 derivative strains Genotype Reference DH5α supE44 D(lacIZYA-argF)U169 deoR (Φ80lacZDM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 Hanahan 1983 DH5α(λ) λ prophage This work DH5α(λΔD::KanR) λΔD::KanR prophage This work DH5α(λΔD) λΔD prophage This work W3110 F- λ - rph- Bachmann 1972 JW2787 F- Δ(araD-araB)567 ΔlacZ4787(::rrnB- 3) λ ΔrecD744::kan rph-1 Δ(rhaD-rhaB)568 hsdR514 Baba et al. 2006 SoluBL21† F- ompT hsdSB (rB- mB-) gal dcm (DE3) Deatherage et al. 2012 Bacteriophages/viral strains Genotype Reference λwt Lambda wild type CSH Collection λcI857 Lambda tscI857 CSH Collection λΔD::KanR λcI857 with a Virus:Article Title: A Lambda-evo (λ evo ) phage platform for Zika virus E DIII protein display Article Snippet: .. Escherichia coli K-12 derivative strains Genotype Reference DH5α supE44 D(lacIZYA-argF)U169 deoR (Φ80lacZDM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 Hanahan 1983 DH5α(λ) λ prophage This work DH5α(λΔD::KanR) λΔD::KanR prophage This work DH5α(λΔD) λΔD prophage This work W3110 F- λ - rph- Bachmann 1972 JW2787 F- Δ(araD-araB)567 ΔlacZ4787(::rrnB- 3) λ ΔrecD744::kan rph-1 Δ(rhaD-rhaB)568 hsdR514 Baba et al. 2006 SoluBL21† F- ompT hsdSB (rB- mB-) gal dcm (DE3) Deatherage et al. 2012 Bacteriophages/viral strains Genotype Reference λwt Lambda wild type CSH Collection λcI857 Lambda tscI857 CSH Collection λΔD::KanR λcI857 with a Plasmid Preparation:Article Title: A Lambda-evo (λ evo ) phage platform for Zika virus E DIII protein display Article Snippet: .. Escherichia coli K-12 derivative strains Genotype Reference DH5α supE44 D(lacIZYA-argF)U169 deoR (Φ80lacZDM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 Hanahan 1983 DH5α(λ) λ prophage This work DH5α(λΔD::KanR) λΔD::KanR prophage This work DH5α(λΔD) λΔD prophage This work W3110 F- λ - rph- Bachmann 1972 JW2787 F- Δ(araD-araB)567 ΔlacZ4787(::rrnB- 3) λ ΔrecD744::kan rph-1 Δ(rhaD-rhaB)568 hsdR514 Baba et al. 2006 SoluBL21† F- ompT hsdSB (rB- mB-) gal dcm (DE3) Deatherage et al. 2012 Bacteriophages/viral strains Genotype Reference λwt Lambda wild type CSH Collection λcI857 Lambda tscI857 CSH Collection λΔD::KanR λcI857 with a Sequencing:Article Title: A Lambda-evo (λ evo ) phage platform for Zika virus E DIII protein display Article Snippet: .. Escherichia coli K-12 derivative strains Genotype Reference DH5α supE44 D(lacIZYA-argF)U169 deoR (Φ80lacZDM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 Hanahan 1983 DH5α(λ) λ prophage This work DH5α(λΔD::KanR) λΔD::KanR prophage This work DH5α(λΔD) λΔD prophage This work W3110 F- λ - rph- Bachmann 1972 JW2787 F- Δ(araD-araB)567 ΔlacZ4787(::rrnB- 3) λ ΔrecD744::kan rph-1 Δ(rhaD-rhaB)568 hsdR514 Baba et al. 2006 SoluBL21† F- ompT hsdSB (rB- mB-) gal dcm (DE3) Deatherage et al. 2012 Bacteriophages/viral strains Genotype Reference λwt Lambda wild type CSH Collection λcI857 Lambda tscI857 CSH Collection λΔD::KanR λcI857 with a Article Title: A MultiSite Gateway Toolkit for Rapid Cloning of Vertebrate Expression Constructs with Diverse Research Applications Article Snippet: .. Unless otherwise stated, all 3’ entry vectors were generated by PCR amplification of the desired 3’ element using attB2R/B3-flanked oligonucleotide primers, followed by a BP reaction with pDONR P2R-P3 (Invitrogen). p3E-GFP-HA, p3E-YFP-HA (from pEYFP-C1, Clontech), p3E-CFP-HA (from pECFP-C1, Clontech), p3E-mCherry-HA (from p3E-mCherrypA [ ]), p3E-mKate2-HA and p3E-mKate2-myc no-polyadenylation signal (pA) were made by amplification of the coding sequences without a stop codon, but with the 3’ primer additionally containing an HA or c-myc epitope sequence followed by a stop codon. p3E-HA-Neuroligin1 was generated by amplification of HA-Neuroligin1 from a previously described vector [ ]. p3E-Dam-myc no-pA is from pNDam-Myc [ ]. p3E-SGTAP no-pA originated from pCeMM-CTAP(SG)-Gw [ ]. p3E-FRT-Kan R -FRT pA was cloned by amplifying the Selection:Article Title: A Lambda-evo (λ evo ) phage platform for Zika virus E DIII protein display Article Snippet: .. Escherichia coli K-12 derivative strains Genotype Reference DH5α supE44 D(lacIZYA-argF)U169 deoR (Φ80lacZDM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 Hanahan 1983 DH5α(λ) λ prophage This work DH5α(λΔD::KanR) λΔD::KanR prophage This work DH5α(λΔD) λΔD prophage This work W3110 F- λ - rph- Bachmann 1972 JW2787 F- Δ(araD-araB)567 ΔlacZ4787(::rrnB- 3) λ ΔrecD744::kan rph-1 Δ(rhaD-rhaB)568 hsdR514 Baba et al. 2006 SoluBL21† F- ompT hsdSB (rB- mB-) gal dcm (DE3) Deatherage et al. 2012 Bacteriophages/viral strains Genotype Reference λwt Lambda wild type CSH Collection λcI857 Lambda tscI857 CSH Collection λΔD::KanR λcI857 with a Generated:Article Title: A MultiSite Gateway Toolkit for Rapid Cloning of Vertebrate Expression Constructs with Diverse Research Applications Article Snippet: .. Unless otherwise stated, all 3’ entry vectors were generated by PCR amplification of the desired 3’ element using attB2R/B3-flanked oligonucleotide primers, followed by a BP reaction with pDONR P2R-P3 (Invitrogen). p3E-GFP-HA, p3E-YFP-HA (from pEYFP-C1, Clontech), p3E-CFP-HA (from pECFP-C1, Clontech), p3E-mCherry-HA (from p3E-mCherrypA [ ]), p3E-mKate2-HA and p3E-mKate2-myc no-polyadenylation signal (pA) were made by amplification of the coding sequences without a stop codon, but with the 3’ primer additionally containing an HA or c-myc epitope sequence followed by a stop codon. p3E-HA-Neuroligin1 was generated by amplification of HA-Neuroligin1 from a previously described vector [ ]. p3E-Dam-myc no-pA is from pNDam-Myc [ ]. p3E-SGTAP no-pA originated from pCeMM-CTAP(SG)-Gw [ ]. p3E-FRT-Kan R -FRT pA was cloned by amplifying the Amplification:Article Title: A MultiSite Gateway Toolkit for Rapid Cloning of Vertebrate Expression Constructs with Diverse Research Applications Article Snippet: .. Unless otherwise stated, all 3’ entry vectors were generated by PCR amplification of the desired 3’ element using attB2R/B3-flanked oligonucleotide primers, followed by a BP reaction with pDONR P2R-P3 (Invitrogen). p3E-GFP-HA, p3E-YFP-HA (from pEYFP-C1, Clontech), p3E-CFP-HA (from pECFP-C1, Clontech), p3E-mCherry-HA (from p3E-mCherrypA [ ]), p3E-mKate2-HA and p3E-mKate2-myc no-polyadenylation signal (pA) were made by amplification of the coding sequences without a stop codon, but with the 3’ primer additionally containing an HA or c-myc epitope sequence followed by a stop codon. p3E-HA-Neuroligin1 was generated by amplification of HA-Neuroligin1 from a previously described vector [ ]. p3E-Dam-myc no-pA is from pNDam-Myc [ ]. p3E-SGTAP no-pA originated from pCeMM-CTAP(SG)-Gw [ ]. p3E-FRT-Kan R -FRT pA was cloned by amplifying the Clone Assay:Article Title: A MultiSite Gateway Toolkit for Rapid Cloning of Vertebrate Expression Constructs with Diverse Research Applications Article Snippet: .. Unless otherwise stated, all 3’ entry vectors were generated by PCR amplification of the desired 3’ element using attB2R/B3-flanked oligonucleotide primers, followed by a BP reaction with pDONR P2R-P3 (Invitrogen). p3E-GFP-HA, p3E-YFP-HA (from pEYFP-C1, Clontech), p3E-CFP-HA (from pECFP-C1, Clontech), p3E-mCherry-HA (from p3E-mCherrypA [ ]), p3E-mKate2-HA and p3E-mKate2-myc no-polyadenylation signal (pA) were made by amplification of the coding sequences without a stop codon, but with the 3’ primer additionally containing an HA or c-myc epitope sequence followed by a stop codon. p3E-HA-Neuroligin1 was generated by amplification of HA-Neuroligin1 from a previously described vector [ ]. p3E-Dam-myc no-pA is from pNDam-Myc [ ]. p3E-SGTAP no-pA originated from pCeMM-CTAP(SG)-Gw [ ]. p3E-FRT-Kan R -FRT pA was cloned by amplifying the |