multiple sequence alignment program sequencher 3.1 (Gene Codes Inc)
90
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Gene Codes Inc
multiple sequence alignment program sequencher 3.1
Multiple Sequence Alignment Program Sequencher 3.1, supplied by Gene Codes Inc, 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/sequence+alignment+programs+sequencher/dna+sequence+assemble+software+sequencher/pm16949311-70-18-23
Average 90 stars, based on 1 article reviews
Multiple Sequence Alignment Program Sequencher 3.1, supplied by Gene Codes Inc, 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/sequence+alignment+programs+sequencher/dna+sequence+assemble+software+sequencher/pm16949311-70-18-23
Average 90 stars, based on 1 article reviews
multiple sequence alignment program sequencher 3.1 - by Bioz Stars,
2026-09
90/100 stars
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Polymerase Chain Reaction:Article Title: Isolated nucleic acids and kits for identifying subjects susceptible to ataxic neurological disease Article Snippet: Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences were aligned with the known exon sequence using a multiple sequence alignment tool, Sequencher (Gene Codes Corporation, Ann Arbor, Mich.), in order to identify any nucleotide changes. .. Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences were aligned with the known exon sequence using a Article Title: Methods for identifying subjects susceptible to charcot-marie-tooth neuropathy type 1C Article Snippet: .. Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences are aligned with the known exon sequence using a Amplification:Article Title: Isolated nucleic acids and kits for identifying subjects susceptible to ataxic neurological disease Article Snippet: Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences were aligned with the known exon sequence using a multiple sequence alignment tool, Sequencher (Gene Codes Corporation, Ann Arbor, Mich.), in order to identify any nucleotide changes. .. Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences were aligned with the known exon sequence using a Article Title: Enzyme associated with equol synthesis Article Snippet: The amplified DNA fragments were excised from the agarose gel, and purified using a Gel-Extraction kit (Qiagen). .. The base sequences of the purified DNA fragments were determined by the direct sequence using the primers used for the amplification, with the result that the sequence of dihydrodaidzein synthesis enzyme gene was observed in those DNA fragments of about 1.2 kb (SacI) and about 1.0 kb (Sau3AI) in 5′-RACE, and that of about 0.6 kb (SacI) in 3′-RACE. (3) Determination of Entire Base Sequence of Dihydrodaidzein Synthesis Enzyme Gene The DNA base sequence obtained by the degenerative-PCR in Example A5 and the rapid amplification of the cDNA terminus sequence in (2) of the present Example was subjected to assemble assay using Article Title: Methods for identifying subjects susceptible to charcot-marie-tooth neuropathy type 1C Article Snippet: .. Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences are aligned with the known exon sequence using a Sequencing:Article Title: Isolated nucleic acids and kits for identifying subjects susceptible to ataxic neurological disease Article Snippet: Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences were aligned with the known exon sequence using a multiple sequence alignment tool, Sequencher (Gene Codes Corporation, Ann Arbor, Mich.), in order to identify any nucleotide changes. .. Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences were aligned with the known exon sequence using a Article Title: Direct Selection of Functional Insulators in Arabidopsis thaliana Article Snippet: .. Bioinformatics DNAMAN (http://www.lynnon.com/) and Article Title: Methods for identifying subjects susceptible to charcot-marie-tooth neuropathy type 1C Article Snippet: .. For example, resulting sequences can be aligned with the known exon sequence using a Article Title: Enzyme associated with equol synthesis Article Snippet: The amplified DNA fragments were excised from the agarose gel, and purified using a Gel-Extraction kit (Qiagen). .. The base sequences of the purified DNA fragments were determined by the direct sequence using the primers used for the amplification, with the result that the sequence of dihydrodaidzein synthesis enzyme gene was observed in those DNA fragments of about 1.2 kb (SacI) and about 1.0 kb (Sau3AI) in 5′-RACE, and that of about 0.6 kb (SacI) in 3′-RACE. (3) Determination of Entire Base Sequence of Dihydrodaidzein Synthesis Enzyme Gene The DNA base sequence obtained by the degenerative-PCR in Example A5 and the rapid amplification of the cDNA terminus sequence in (2) of the present Example was subjected to assemble assay using Article Title: Enzyme associated with equol synthesis Article Snippet: The purified DNA fragment was inserted to a pT7-Blue Cloning Vector (Novagen) to determine the base sequence. .. The obtained DNA base sequence was assayed using Article Title: Methods for identifying subjects susceptible to charcot-marie-tooth neuropathy type 1C Article Snippet: .. Methods Utilized: PCR Amplification: Carried out as described in Example 1 Direct Sequencing: Carried out as described in Example 1 Data Analysis: The resulting sequences are aligned with the known exon sequence using a Article Title: Methods and related compositions for manufacturing food and feed Article Snippet: .. DNA Sequencing:Article Title: Direct Selection of Functional Insulators in Arabidopsis thaliana Article Snippet: .. Bioinformatics DNAMAN (http://www.lynnon.com/) and other:Article Title: Adaptation to cell culture induces functional differences in measles virus proteins Article Snippet: Sequence data were analyzed with the Purification:Article Title: Enzyme associated with equol synthesis Article Snippet: The amplified DNA fragments were excised from the agarose gel, and purified using a Gel-Extraction kit (Qiagen). .. The base sequences of the purified DNA fragments were determined by the direct sequence using the primers used for the amplification, with the result that the sequence of dihydrodaidzein synthesis enzyme gene was observed in those DNA fragments of about 1.2 kb (SacI) and about 1.0 kb (Sau3AI) in 5′-RACE, and that of about 0.6 kb (SacI) in 3′-RACE. (3) Determination of Entire Base Sequence of Dihydrodaidzein Synthesis Enzyme Gene The DNA base sequence obtained by the degenerative-PCR in Example A5 and the rapid amplification of the cDNA terminus sequence in (2) of the present Example was subjected to assemble assay using Software:Article Title: Enzyme associated with equol synthesis Article Snippet: The amplified DNA fragments were excised from the agarose gel, and purified using a Gel-Extraction kit (Qiagen). .. The base sequences of the purified DNA fragments were determined by the direct sequence using the primers used for the amplification, with the result that the sequence of dihydrodaidzein synthesis enzyme gene was observed in those DNA fragments of about 1.2 kb (SacI) and about 1.0 kb (Sau3AI) in 5′-RACE, and that of about 0.6 kb (SacI) in 3′-RACE. (3) Determination of Entire Base Sequence of Dihydrodaidzein Synthesis Enzyme Gene The DNA base sequence obtained by the degenerative-PCR in Example A5 and the rapid amplification of the cDNA terminus sequence in (2) of the present Example was subjected to assemble assay using Article Title: Enzyme associated with equol synthesis Article Snippet: The purified DNA fragment was inserted to a pT7-Blue Cloning Vector (Novagen) to determine the base sequence. .. The obtained DNA base sequence was assayed using Article Title: Methods and related compositions for manufacturing food and feed Article Snippet: .. |