yeast gal4 dna binding domain expression vector pas2 1 (TaKaRa)
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yeast gal4 dna binding domain expression vector pas2 1
Yeast Gal4 Dna Binding Domain Expression Vector Pas2 1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 619 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/yeast+vector+pas2+1/pmCherry+Vector/pmc03695902-56-6-14
Average 96 stars, based on 619 article reviews
Yeast Gal4 Dna Binding Domain Expression Vector Pas2 1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 619 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/yeast+vector+pas2+1/pmCherry+Vector/pmc03695902-56-6-14
Average 96 stars, based on 619 article reviews
yeast gal4 dna binding domain expression vector pas2 1 - by Bioz Stars,
2026-09
96/100 stars
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Amplification:Article Title: Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication. Article Snippet: .. The truncated KIFC5A-s, amplified from mouse E13 hippocampal cDNA with oligo set 2, was transferred as a BamHI fragment into bacterial expression vector pHAT2 (Peränen et al., 1996) and from there as an EcoRI fragment into Article Title: Protein Kinase A-anchoring Protein AKAP95 Interacts with MCM2, a Regulator of DNA Replication Article Snippet: .. Yeast Two-hybrid Screening—As bait, a full-length AKAP95 was amplified by PCR (9) and subcloned into Article Title: Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication. Article Snippet: From pCR2.1, it was subcloned in-frame as an EcoRI fragment in yeast vector pACT2 (Clontech). .. The cDNA of Nubp2, amplified from NIH 3T3 with oligo set 9, was initially transferred by T/A cloning into bacterial vector pCR2.1 (Invitrogen) and then subcloned as an EcoRI fragment into mammalian transfection vector pEGFP-N2 (BD Biosciences) and Article Title: The KSHV immediate-early transcription factor RTA encodes ubiquitin E3 ligase activity that targets IRF7 for proteosome-mediated degradation. Article Snippet: .. The GAL4-RTA(1–544) DNA binding domain fusion protein in plasmidE6 (Scheffner et al., 1993). pYXY1 was generated in the Expressing:Article Title: Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication. Article Snippet: .. The truncated KIFC5A-s, amplified from mouse E13 hippocampal cDNA with oligo set 2, was transferred as a BamHI fragment into bacterial expression vector pHAT2 (Peränen et al., 1996) and from there as an EcoRI fragment into Plasmid Preparation:Article Title: Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication. Article Snippet: .. The truncated KIFC5A-s, amplified from mouse E13 hippocampal cDNA with oligo set 2, was transferred as a BamHI fragment into bacterial expression vector pHAT2 (Peränen et al., 1996) and from there as an EcoRI fragment into Article Title: Protein Kinase A-anchoring Protein AKAP95 Interacts with MCM2, a Regulator of DNA Replication Article Snippet: .. Yeast Two-hybrid Screening—As bait, a full-length AKAP95 was amplified by PCR (9) and subcloned into Article Title: The KSHV immediate-early transcription factor RTA encodes ubiquitin E3 ligase activity that targets IRF7 for proteosome-mediated degradation. Article Snippet: .. The GAL4-RTA(1–544) DNA binding domain fusion protein in plasmidE6 (Scheffner et al., 1993). pYXY1 was generated in the Polymerase Chain Reaction:Article Title: Protein Kinase A-anchoring Protein AKAP95 Interacts with MCM2, a Regulator of DNA Replication Article Snippet: .. Yeast Two-hybrid Screening—As bait, a full-length AKAP95 was amplified by PCR (9) and subcloned into Cloning:Article Title: Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication. Article Snippet: From pCR2.1, it was subcloned in-frame as an EcoRI fragment in yeast vector pACT2 (Clontech). .. The cDNA of Nubp2, amplified from NIH 3T3 with oligo set 9, was initially transferred by T/A cloning into bacterial vector pCR2.1 (Invitrogen) and then subcloned as an EcoRI fragment into mammalian transfection vector pEGFP-N2 (BD Biosciences) and Transfection:Article Title: Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication. Article Snippet: From pCR2.1, it was subcloned in-frame as an EcoRI fragment in yeast vector pACT2 (Clontech). .. The cDNA of Nubp2, amplified from NIH 3T3 with oligo set 9, was initially transferred by T/A cloning into bacterial vector pCR2.1 (Invitrogen) and then subcloned as an EcoRI fragment into mammalian transfection vector pEGFP-N2 (BD Biosciences) and Binding Assay:Article Title: The KSHV immediate-early transcription factor RTA encodes ubiquitin E3 ligase activity that targets IRF7 for proteosome-mediated degradation. Article Snippet: .. The GAL4-RTA(1–544) DNA binding domain fusion protein in plasmidE6 (Scheffner et al., 1993). pYXY1 was generated in the Generated:Article Title: The KSHV immediate-early transcription factor RTA encodes ubiquitin E3 ligase activity that targets IRF7 for proteosome-mediated degradation. Article Snippet: .. The GAL4-RTA(1–544) DNA binding domain fusion protein in plasmidE6 (Scheffner et al., 1993). pYXY1 was generated in the Cotransfection:Article Title: The KSHV immediate-early transcription factor RTA encodes ubiquitin E3 ligase activity that targets IRF7 for proteosome-mediated degradation. Article Snippet: .. The GAL4-RTA(1–544) DNA binding domain fusion protein in plasmidE6 (Scheffner et al., 1993). pYXY1 was generated in the Mutagenesis:Article Title: The KSHV immediate-early transcription factor RTA encodes ubiquitin E3 ligase activity that targets IRF7 for proteosome-mediated degradation. Article Snippet: .. The GAL4-RTA(1–544) DNA binding domain fusion protein in plasmidE6 (Scheffner et al., 1993). pYXY1 was generated in the |