primer extension system kit (Promega)
90
Structured Review
Promega
primer extension system kit
Primer Extension System Kit, supplied by Promega, 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/primer+extension+kit/primer+extension+kit/pm37046126-33-23-27
Average 90 stars, based on 1 article reviews
Primer Extension System Kit, supplied by Promega, 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/primer+extension+kit/primer+extension+kit/pm37046126-33-23-27
Average 90 stars, based on 1 article reviews
primer extension system kit - by Bioz Stars,
2026-10
90/100 stars
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Selection:Article Title: Selection of optimal antisense accessible sites of uroplakin II mRNA for bladder urothelium. Article Snippet: The optimal antisense accessible sites (AAS) of uroplakin II (UPII) mRNA, a specific gene expressed in bladder urothelium, were selected in order to provide a novel method for targeted therapy of transitional cell carcinoma (TCC) of bladder.. The 20 mer random oligonucleotide library was synthesized, hybridized with in vitro transcripted total UPII cRNA, then digested by RNase H. After primer extension and autoradiography, the AAS of UPII were selected.. The RNADraw software was used to analyze and choose the AAS with obvious stem-loop structures, according to which the complementary antisense oligonucleotides (AS-ODN) were synthesized. Atomic Absorption Spectroscopy:Article Title: Selection of optimal antisense accessible sites of uroplakin II mRNA for bladder urothelium. Article Snippet: The optimal antisense accessible sites (AAS) of uroplakin II (UPII) mRNA, a specific gene expressed in bladder urothelium, were selected in order to provide a novel method for targeted therapy of transitional cell carcinoma (TCC) of bladder.. The 20 mer random oligonucleotide library was synthesized, hybridized with in vitro transcripted total UPII cRNA, then digested by RNase H. After primer extension and autoradiography, the AAS of UPII were selected.. The RNADraw software was used to analyze and choose the AAS with obvious stem-loop structures, according to which the complementary antisense oligonucleotides (AS-ODN) were synthesized. Sequencing:Article Title: Selection of optimal antisense accessible sites of uroplakin II mRNA for bladder urothelium. Article Snippet: The optimal antisense accessible sites (AAS) of uroplakin II (UPII) mRNA, a specific gene expressed in bladder urothelium, were selected in order to provide a novel method for targeted therapy of transitional cell carcinoma (TCC) of bladder.. The 20 mer random oligonucleotide library was synthesized, hybridized with in vitro transcripted total UPII cRNA, then digested by RNase H. After primer extension and autoradiography, the AAS of UPII were selected.. The RNADraw software was used to analyze and choose the AAS with obvious stem-loop structures, according to which the complementary antisense oligonucleotides (AS-ODN) were synthesized. Article Title: Stress-induced mobility of OPHIO1 and OPHIO2, DNA transposons of the Dutch elm disease fungi. Article Snippet: The mobility of transposable elements (TEs) can contribute to genome plasticity, underor over-expression of genes and ectopic recombination.. The data collected in this study provide evidence of stress-induced mobility of OPHIO1 and OPHIO2 transposons, recently detected in Ophiostoma ulmi and O. novo-ulmi, the causal agents of Dutch elm disease (DED).. The analyses of OPHIO UTRs and TIRs indicated the presence of two potential binding site motifs and a heat shock protein (hsp) promoter which could be involved in the mobility of OPHIO1 following a heat shock stress. Software:Article Title: Selection of optimal antisense accessible sites of uroplakin II mRNA for bladder urothelium. Article Snippet: The optimal antisense accessible sites (AAS) of uroplakin II (UPII) mRNA, a specific gene expressed in bladder urothelium, were selected in order to provide a novel method for targeted therapy of transitional cell carcinoma (TCC) of bladder.. The 20 mer random oligonucleotide library was synthesized, hybridized with in vitro transcripted total UPII cRNA, then digested by RNase H. After primer extension and autoradiography, the AAS of UPII were selected.. The RNADraw software was used to analyze and choose the AAS with obvious stem-loop structures, according to which the complementary antisense oligonucleotides (AS-ODN) were synthesized. Synthesized:Article Title: Selection of optimal antisense accessible sites of uroplakin II mRNA for bladder urothelium. Article Snippet: The optimal antisense accessible sites (AAS) of uroplakin II (UPII) mRNA, a specific gene expressed in bladder urothelium, were selected in order to provide a novel method for targeted therapy of transitional cell carcinoma (TCC) of bladder.. The 20 mer random oligonucleotide library was synthesized, hybridized with in vitro transcripted total UPII cRNA, then digested by RNase H. After primer extension and autoradiography, the AAS of UPII were selected.. The RNADraw software was used to analyze and choose the AAS with obvious stem-loop structures, according to which the complementary antisense oligonucleotides (AS-ODN) were synthesized. Concentration Assay:Article Title: Selection of optimal antisense accessible sites of uroplakin II mRNA for bladder urothelium. Article Snippet: The optimal antisense accessible sites (AAS) of uroplakin II (UPII) mRNA, a specific gene expressed in bladder urothelium, were selected in order to provide a novel method for targeted therapy of transitional cell carcinoma (TCC) of bladder.. The 20 mer random oligonucleotide library was synthesized, hybridized with in vitro transcripted total UPII cRNA, then digested by RNase H. After primer extension and autoradiography, the AAS of UPII were selected.. The RNADraw software was used to analyze and choose the AAS with obvious stem-loop structures, according to which the complementary antisense oligonucleotides (AS-ODN) were synthesized. Rapid Amplification of cDNA Ends:Article Title: Stress-induced mobility of OPHIO1 and OPHIO2, DNA transposons of the Dutch elm disease fungi. Article Snippet: The mobility of transposable elements (TEs) can contribute to genome plasticity, underor over-expression of genes and ectopic recombination.. The data collected in this study provide evidence of stress-induced mobility of OPHIO1 and OPHIO2 transposons, recently detected in Ophiostoma ulmi and O. novo-ulmi, the causal agents of Dutch elm disease (DED).. The analyses of OPHIO UTRs and TIRs indicated the presence of two potential binding site motifs and a heat shock protein (hsp) promoter which could be involved in the mobility of OPHIO1 following a heat shock stress. Polymerase Chain Reaction:Article Title: Stress-induced mobility of OPHIO1 and OPHIO2, DNA transposons of the Dutch elm disease fungi. Article Snippet: The mobility of transposable elements (TEs) can contribute to genome plasticity, underor over-expression of genes and ectopic recombination.. The data collected in this study provide evidence of stress-induced mobility of OPHIO1 and OPHIO2 transposons, recently detected in Ophiostoma ulmi and O. novo-ulmi, the causal agents of Dutch elm disease (DED).. The analyses of OPHIO UTRs and TIRs indicated the presence of two potential binding site motifs and a heat shock protein (hsp) promoter which could be involved in the mobility of OPHIO1 following a heat shock stress. |