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Macrogen total genomic dna samples
Total Genomic Dna Samples, supplied by Macrogen, 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/result/total genomic dna samples/product/Macrogen
Average 90 stars, based on 1 article reviews
total genomic dna samples - by Bioz Stars, 2026-05
90/100 stars

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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 .
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Qiagen total genomic dna from modern samples was extracted
( 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 Genomic Dna From Modern Samples Was Extracted, supplied by Qiagen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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