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total purified genomic dna samples  (Thermo Fisher)


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    Structured Review

    Thermo Fisher total purified genomic dna samples
    ( a ) RT-PCR analyses of transcripts for ABI5 . A PCR product of the ONSEN insertion site was not amplified in the 13–7 ibm2 and 13–7 parent line because of transcription elongation defects. In contrast, the first intron was spliced out in 13–7 and 13–7 nrpd1 of F3, similarly to the wild type. ABI5 1 st intron; the first intron that ONSEN was inserted in 13–7. 18S; 18S rRNA gene. <t>Genomic</t> <t>DNA</t> <t>(gDNA)</t> was used as a template. The red arrowhead indicates an ONSEN insertion. ( b ) A 3′ Rapid Amplification of cDNA Ends (RACE) of ABI5 in the F3 progeny. The red arrowhead indicates an ONSEN insertion and black arrows indicate primers used in 3′ RACE. ( c ) Bisulfite sequence analysis of 5′ and 3′ flanking regions of the ONSEN insertion in F3 progenies (derived from the progeny of a cross between 13–7 and an ibm2 ). 13–7 : F3 progeny that contains an ONSEN insertion in ABI5 . 13–7 ibm2 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in IBM2 . 13–7 nrpd1 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in NRPD1 .
    Total Purified Genomic Dna Samples, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total purified genomic dna samples/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    total purified genomic dna samples - by Bioz Stars, 2026-06
    99/100 stars

    Images

    1) Product Images from "A Stress-Activated Transposon in Arabidopsis Induces Transgenerational Abscisic Acid Insensitivity"

    Article Title: A Stress-Activated Transposon in Arabidopsis Induces Transgenerational Abscisic Acid Insensitivity

    Journal: Scientific Reports

    doi: 10.1038/srep23181

    ( a ) RT-PCR analyses of transcripts for ABI5 . A PCR product of the ONSEN insertion site was not amplified in the 13–7 ibm2 and 13–7 parent line because of transcription elongation defects. In contrast, the first intron was spliced out in 13–7 and 13–7 nrpd1 of F3, similarly to the wild type. ABI5 1 st intron; the first intron that ONSEN was inserted in 13–7. 18S; 18S rRNA gene. Genomic DNA (gDNA) was used as a template. The red arrowhead indicates an ONSEN insertion. ( b ) A 3′ Rapid Amplification of cDNA Ends (RACE) of ABI5 in the F3 progeny. The red arrowhead indicates an ONSEN insertion and black arrows indicate primers used in 3′ RACE. ( c ) Bisulfite sequence analysis of 5′ and 3′ flanking regions of the ONSEN insertion in F3 progenies (derived from the progeny of a cross between 13–7 and an ibm2 ). 13–7 : F3 progeny that contains an ONSEN insertion in ABI5 . 13–7 ibm2 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in IBM2 . 13–7 nrpd1 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in NRPD1 .
    Figure Legend Snippet: ( a ) RT-PCR analyses of transcripts for ABI5 . A PCR product of the ONSEN insertion site was not amplified in the 13–7 ibm2 and 13–7 parent line because of transcription elongation defects. In contrast, the first intron was spliced out in 13–7 and 13–7 nrpd1 of F3, similarly to the wild type. ABI5 1 st intron; the first intron that ONSEN was inserted in 13–7. 18S; 18S rRNA gene. Genomic DNA (gDNA) was used as a template. The red arrowhead indicates an ONSEN insertion. ( b ) A 3′ Rapid Amplification of cDNA Ends (RACE) of ABI5 in the F3 progeny. The red arrowhead indicates an ONSEN insertion and black arrows indicate primers used in 3′ RACE. ( c ) Bisulfite sequence analysis of 5′ and 3′ flanking regions of the ONSEN insertion in F3 progenies (derived from the progeny of a cross between 13–7 and an ibm2 ). 13–7 : F3 progeny that contains an ONSEN insertion in ABI5 . 13–7 ibm2 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in IBM2 . 13–7 nrpd1 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in NRPD1 .

    Techniques Used: Reverse Transcription Polymerase Chain Reaction, Amplification, Rapid Amplification of cDNA Ends, Sequencing, Derivative Assay, Mutagenesis



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    Thermo Fisher total purified genomic dna samples
    ( a ) RT-PCR analyses of transcripts for ABI5 . A PCR product of the ONSEN insertion site was not amplified in the 13–7 ibm2 and 13–7 parent line because of transcription elongation defects. In contrast, the first intron was spliced out in 13–7 and 13–7 nrpd1 of F3, similarly to the wild type. ABI5 1 st intron; the first intron that ONSEN was inserted in 13–7. 18S; 18S rRNA gene. <t>Genomic</t> <t>DNA</t> <t>(gDNA)</t> was used as a template. The red arrowhead indicates an ONSEN insertion. ( b ) A 3′ Rapid Amplification of cDNA Ends (RACE) of ABI5 in the F3 progeny. The red arrowhead indicates an ONSEN insertion and black arrows indicate primers used in 3′ RACE. ( c ) Bisulfite sequence analysis of 5′ and 3′ flanking regions of the ONSEN insertion in F3 progenies (derived from the progeny of a cross between 13–7 and an ibm2 ). 13–7 : F3 progeny that contains an ONSEN insertion in ABI5 . 13–7 ibm2 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in IBM2 . 13–7 nrpd1 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in NRPD1 .
    Total Purified Genomic Dna Samples, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total purified genomic dna samples/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    total purified genomic dna samples - by Bioz Stars, 2026-06
    99/100 stars
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    ( a ) RT-PCR analyses of transcripts for ABI5 . A PCR product of the ONSEN insertion site was not amplified in the 13–7 ibm2 and 13–7 parent line because of transcription elongation defects. In contrast, the first intron was spliced out in 13–7 and 13–7 nrpd1 of F3, similarly to the wild type. ABI5 1 st intron; the first intron that ONSEN was inserted in 13–7. 18S; 18S rRNA gene. Genomic DNA (gDNA) was used as a template. The red arrowhead indicates an ONSEN insertion. ( b ) A 3′ Rapid Amplification of cDNA Ends (RACE) of ABI5 in the F3 progeny. The red arrowhead indicates an ONSEN insertion and black arrows indicate primers used in 3′ RACE. ( c ) Bisulfite sequence analysis of 5′ and 3′ flanking regions of the ONSEN insertion in F3 progenies (derived from the progeny of a cross between 13–7 and an ibm2 ). 13–7 : F3 progeny that contains an ONSEN insertion in ABI5 . 13–7 ibm2 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in IBM2 . 13–7 nrpd1 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in NRPD1 .

    Journal: Scientific Reports

    Article Title: A Stress-Activated Transposon in Arabidopsis Induces Transgenerational Abscisic Acid Insensitivity

    doi: 10.1038/srep23181

    Figure Lengend Snippet: ( a ) RT-PCR analyses of transcripts for ABI5 . A PCR product of the ONSEN insertion site was not amplified in the 13–7 ibm2 and 13–7 parent line because of transcription elongation defects. In contrast, the first intron was spliced out in 13–7 and 13–7 nrpd1 of F3, similarly to the wild type. ABI5 1 st intron; the first intron that ONSEN was inserted in 13–7. 18S; 18S rRNA gene. Genomic DNA (gDNA) was used as a template. The red arrowhead indicates an ONSEN insertion. ( b ) A 3′ Rapid Amplification of cDNA Ends (RACE) of ABI5 in the F3 progeny. The red arrowhead indicates an ONSEN insertion and black arrows indicate primers used in 3′ RACE. ( c ) Bisulfite sequence analysis of 5′ and 3′ flanking regions of the ONSEN insertion in F3 progenies (derived from the progeny of a cross between 13–7 and an ibm2 ). 13–7 : F3 progeny that contains an ONSEN insertion in ABI5 . 13–7 ibm2 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in IBM2 . 13–7 nrpd1 : F3 progeny that contains an ONSEN insertion in ABI5 and a mutation in NRPD1 .

    Article Snippet: Total purified genomic DNA samples (1 μg) were processed into pair-endo sequencing libraries using the SOLiD fragment library construction kit (Life Technologies).

    Techniques: Reverse Transcription Polymerase Chain Reaction, Amplification, Rapid Amplification of cDNA Ends, Sequencing, Derivative Assay, Mutagenesis