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ds gene computer program  (Accelrys)

 
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    Accelrys ds gene computer program
    Figure 5: Genomic products; E5, E6. PCR amplification of regions within the grin1b <t>gene</t> corresponding to E5 and E6 potential RNA editing sites. As predicted by the DS Gene <t>computer</t> <t>program</t> (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides. Primers aimed at amplifying the genomic E6 sequence (ZF.Grin1bE6.F1 and ZF.Grin1bE6.R1) produced a strong band at around 220 nucleotides. Both of these bands were extracted for sequencing reactions. Amplicons from genomic DNA show no evidence of A/G polymorphism (A only). Dashed black lines represent noise levels per sample.
    Ds Gene Computer Program, supplied by Accelrys, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ds gene computer program/product/Accelrys
    Average 86 stars, based on 1 article reviews
    ds gene computer program - by Bioz Stars, 2026-05
    86/100 stars

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    1) Product Images from "Identification and characterization of two novel RNA editing sites in grin1b transcripts of embryonic Danio rerio."

    Article Title: Identification and characterization of two novel RNA editing sites in grin1b transcripts of embryonic Danio rerio.

    Journal: Neural plasticity

    doi: 10.1155/2012/173728

    Figure 5: Genomic products; E5, E6. PCR amplification of regions within the grin1b gene corresponding to E5 and E6 potential RNA editing sites. As predicted by the DS Gene computer program (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides. Primers aimed at amplifying the genomic E6 sequence (ZF.Grin1bE6.F1 and ZF.Grin1bE6.R1) produced a strong band at around 220 nucleotides. Both of these bands were extracted for sequencing reactions. Amplicons from genomic DNA show no evidence of A/G polymorphism (A only). Dashed black lines represent noise levels per sample.
    Figure Legend Snippet: Figure 5: Genomic products; E5, E6. PCR amplification of regions within the grin1b gene corresponding to E5 and E6 potential RNA editing sites. As predicted by the DS Gene computer program (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides. Primers aimed at amplifying the genomic E6 sequence (ZF.Grin1bE6.F1 and ZF.Grin1bE6.R1) produced a strong band at around 220 nucleotides. Both of these bands were extracted for sequencing reactions. Amplicons from genomic DNA show no evidence of A/G polymorphism (A only). Dashed black lines represent noise levels per sample.

    Techniques Used: Sequencing, Produced



    Similar Products

    ds gene computer program  (Accelrys)
    86
    Accelrys ds gene computer program
    Figure 5: Genomic products; E5, E6. PCR amplification of regions within the grin1b <t>gene</t> corresponding to E5 and E6 potential RNA editing sites. As predicted by the DS Gene <t>computer</t> <t>program</t> (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides. Primers aimed at amplifying the genomic E6 sequence (ZF.Grin1bE6.F1 and ZF.Grin1bE6.R1) produced a strong band at around 220 nucleotides. Both of these bands were extracted for sequencing reactions. Amplicons from genomic DNA show no evidence of A/G polymorphism (A only). Dashed black lines represent noise levels per sample.
    Ds Gene Computer Program, supplied by Accelrys, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ds gene computer program/product/Accelrys
    Average 86 stars, based on 1 article reviews
    ds gene computer program - by Bioz Stars, 2026-05
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    Figure 5: Genomic products; E5, E6. PCR amplification of regions within the grin1b gene corresponding to E5 and E6 potential RNA editing sites. As predicted by the DS Gene computer program (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides. Primers aimed at amplifying the genomic E6 sequence (ZF.Grin1bE6.F1 and ZF.Grin1bE6.R1) produced a strong band at around 220 nucleotides. Both of these bands were extracted for sequencing reactions. Amplicons from genomic DNA show no evidence of A/G polymorphism (A only). Dashed black lines represent noise levels per sample.

    Journal: Neural plasticity

    Article Title: Identification and characterization of two novel RNA editing sites in grin1b transcripts of embryonic Danio rerio.

    doi: 10.1155/2012/173728

    Figure Lengend Snippet: Figure 5: Genomic products; E5, E6. PCR amplification of regions within the grin1b gene corresponding to E5 and E6 potential RNA editing sites. As predicted by the DS Gene computer program (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides. Primers aimed at amplifying the genomic E6 sequence (ZF.Grin1bE6.F1 and ZF.Grin1bE6.R1) produced a strong band at around 220 nucleotides. Both of these bands were extracted for sequencing reactions. Amplicons from genomic DNA show no evidence of A/G polymorphism (A only). Dashed black lines represent noise levels per sample.

    Article Snippet: As predicted by the DS Gene computer program (Accelrys), primers designed to target the genomic E5 sequence (ZF.Grin1bE5.F1 and ZF.Grin1bE5.R1) produced a strong band at around 200 nucleotides.

    Techniques: Sequencing, Produced