plasmid pgbkt7 (TaKaRa)
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TaKaRa
plasmid pgbkt7
Plasmid Pgbkt7, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 4607 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/vector+pgbkt7+bd/pGBKT7+DNA-BD+Vector/pm42827260-412-55-57
Average 99 stars, based on 4607 article reviews
Plasmid Pgbkt7, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 4607 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/vector+pgbkt7+bd/pGBKT7+DNA-BD+Vector/pm42827260-412-55-57
Average 99 stars, based on 4607 article reviews
plasmid pgbkt7 - by Bioz Stars,
2026-10
99/100 stars
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Amplification:Article Title: Non-canonical role of a PHOSPHATE1 HOMOLOG 2 in suppressing seedling photomorphogenesis via the TOC1–PIF4 module Article Snippet: .. The PHO1;H2 (2424bp) was amplified and digested with Xma1 and BamH1 , followed by ligation into the Ligation:Article Title: Non-canonical role of a PHOSPHATE1 HOMOLOG 2 in suppressing seedling photomorphogenesis via the TOC1–PIF4 module Article Snippet: .. The PHO1;H2 (2424bp) was amplified and digested with Xma1 and BamH1 , followed by ligation into the Binding Assay:Article Title: Non-canonical role of a PHOSPHATE1 HOMOLOG 2 in suppressing seedling photomorphogenesis via the TOC1–PIF4 module Article Snippet: .. The PHO1;H2 (2424bp) was amplified and digested with Xma1 and BamH1 , followed by ligation into the Transactivation Assay:Article Title: Coordinated control for the auricle asymmetric development by ZmIDD14 and ZmIDD15 fine-tune the high-density planting adaption in maize. Article Snippet: The fluorescent signal was visualized using an FV1200 confocal laser scanning microscope (Olympus, Tokyo, Japan) with a 488-nm laser line for GFP and a 552-nm laser line for mCherry. .. For the transactivation assay, the full-length coding sequences of ZmIDD14 and ZmIDD15 were separately cloned into the Article Title: Coordinated control for the auricle asymmetric development by ZmIDD14 and ZmIDD15 fine‐tune the high‐density planting adaption in maize Article Snippet: The fluorescent signal was visualized using an FV1200 confocal laser scanning microscope (Olympus, Tokyo, Japan) with a 488‐nm laser line for GFP and a 552‐nm laser line for mCherry. .. For the transactivation assay, the full‐length coding sequences of ZmIDD14 and ZmIDD15 were separately cloned into the Clone Assay:Article Title: Coordinated control for the auricle asymmetric development by ZmIDD14 and ZmIDD15 fine-tune the high-density planting adaption in maize. Article Snippet: The fluorescent signal was visualized using an FV1200 confocal laser scanning microscope (Olympus, Tokyo, Japan) with a 488-nm laser line for GFP and a 552-nm laser line for mCherry. .. For the transactivation assay, the full-length coding sequences of ZmIDD14 and ZmIDD15 were separately cloned into the Article Title: Coordinated control for the auricle asymmetric development by ZmIDD14 and ZmIDD15 fine‐tune the high‐density planting adaption in maize Article Snippet: The fluorescent signal was visualized using an FV1200 confocal laser scanning microscope (Olympus, Tokyo, Japan) with a 488‐nm laser line for GFP and a 552‐nm laser line for mCherry. .. For the transactivation assay, the full‐length coding sequences of ZmIDD14 and ZmIDD15 were separately cloned into the Cloning:Article Title: Coordinated control for the auricle asymmetric development by ZmIDD14 and ZmIDD15 fine-tune the high-density planting adaption in maize. Article Snippet: The fluorescent signal was visualized using an FV1200 confocal laser scanning microscope (Olympus, Tokyo, Japan) with a 488-nm laser line for GFP and a 552-nm laser line for mCherry. .. For the transactivation assay, the full-length coding sequences of ZmIDD14 and ZmIDD15 were separately cloned into the Article Title: Coordinated control for the auricle asymmetric development by ZmIDD14 and ZmIDD15 fine‐tune the high‐density planting adaption in maize Article Snippet: The fluorescent signal was visualized using an FV1200 confocal laser scanning microscope (Olympus, Tokyo, Japan) with a 488‐nm laser line for GFP and a 552‐nm laser line for mCherry. .. For the transactivation assay, the full‐length coding sequences of ZmIDD14 and ZmIDD15 were separately cloned into the Article Title: Importin-β From the Recretohalophyte Limonium bicolor Enhances Salt Tolerance in Arabidopsis thaliana by Reducing Root Hair Development and Abscisic Acid Sensitivity Article Snippet: .. The ORF of LbSAD2 was introduced into the |
![Yeast 2‐hybrid interaction assay of the interaction between (a) TrAP from ToLCNDV‐C ([C]), ToLCNDV‐T&C ([T&C]), ToLCKV‐T ([T]) and ToLCNDV‐C[M9] ([C‐M9]) and SlAGO1, CsAGO1, Slrgs‐CaM and SlATG7. (b) REn from ToLCNDV‐C, ToLCNDV‐T&C, ToLCKV‐T and ToLCNDV‐C[M9] and SlPolA, SlRBR, CsPCNA and SlPCNA. TrAP was expressed as a <t>GAL4‐activating</t> domain fusion protein in HGold yeast and mated with Y187 yeast expressing the plant protein as a fusion protein to the GAL4‐DNA binding domain. The figure shows the mated yeast plated on triple dropout (−Trp/−Leu/−His) plates as selection for interaction. Empty vector controls are HGold expressing the empty vector pGADT7‐AD or Y187 expressing the empty pGBKT7‐BD vector.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_8646/pmc12948646/pmc12948646__MPP-27-e70202-g007.jpg)