random hexanucleotide primer Search Results


random hexanucleotide primer  (Promega)
90
Promega random hexanucleotide primer
Random Hexanucleotide Primer, 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
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hexanucleotide random primers  (Qiagen)
90
Qiagen hexanucleotide random primers
Hexanucleotide Random Primers, 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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hexanucleotide random primers - by Bioz Stars, 2026-03
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random hexamer primer mix  (Carl Roth GmbH)
90
Carl Roth GmbH random hexamer primer mix
Random Hexamer Primer Mix, supplied by Carl Roth GmbH, 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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reverta kit containing m-mlv reverse transcriptase, random hexanucleotide primers, and total rna  (InterLabService)
90
InterLabService reverta kit containing m-mlv reverse transcriptase, random hexanucleotide primers, and total rna
Reverta Kit Containing M Mlv Reverse Transcriptase, Random Hexanucleotide Primers, And Total Rna, supplied by InterLabService, 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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reverta kit containing m-mlv reverse transcriptase, random hexanucleotide primers, and total rna - by Bioz Stars, 2026-03
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oligo-dt- und hexanucleotide-random primers  (Promega)
90
Promega oligo-dt- und hexanucleotide-random primers
Oligo Dt Und Hexanucleotide Random Primers, 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
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Average 90 stars, based on 1 article reviews
oligo-dt- und hexanucleotide-random primers - by Bioz Stars, 2026-03
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labeled by primer extension from random hexanucleotides  (Boehringer Mannheim)
90
Boehringer Mannheim labeled by primer extension from random hexanucleotides
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Labeled By Primer Extension From Random Hexanucleotides, supplied by Boehringer Mannheim, 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/labeled by primer extension from random hexanucleotides/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
labeled by primer extension from random hexanucleotides - by Bioz Stars, 2026-03
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random hexanucleotide primers prime-a-gene  (Promega)
90
Promega random hexanucleotide primers prime-a-gene
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Random Hexanucleotide Primers Prime A Gene, 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
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random hexanucleotide primers prime-a-gene - by Bioz Stars, 2026-03
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hexanucleotide random primers  (Meridian Bioscience)
90
Meridian Bioscience hexanucleotide random primers
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Hexanucleotide Random Primers, supplied by Meridian Bioscience, 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/hexanucleotide random primers/product/Meridian Bioscience
Average 90 stars, based on 1 article reviews
hexanucleotide random primers - by Bioz Stars, 2026-03
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formamide and random primer hexanucleotides pd(n)6  (Boehringer Mannheim)
90
Boehringer Mannheim formamide and random primer hexanucleotides pd(n)6
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Formamide And Random Primer Hexanucleotides Pd(N)6, supplied by Boehringer Mannheim, 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/formamide and random primer hexanucleotides pd(n)6/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
formamide and random primer hexanucleotides pd(n)6 - by Bioz Stars, 2026-03
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random hexanucleotide-primer kit  (Promega)
90
Promega random hexanucleotide-primer kit
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Random Hexanucleotide Primer 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
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Average 90 stars, based on 1 article reviews
random hexanucleotide-primer kit - by Bioz Stars, 2026-03
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hexanucleotides 6-random random hexa primer d0300  (Sileks GmbH)
90
Sileks GmbH hexanucleotides 6-random random hexa primer d0300
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Hexanucleotides 6 Random Random Hexa Primer D0300, supplied by Sileks GmbH, 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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hexanucleotides 6-random random hexa primer d0300 - by Bioz Stars, 2026-03
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random sequence hexanucleotide primers dna labelling megaprime kit  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc random sequence hexanucleotide primers dna labelling megaprime kit
Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random <t>hexanucleotides</t> (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.
Random Sequence Hexanucleotide Primers Dna Labelling Megaprime Kit, supplied by Amersham Life Sciences 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/result/random sequence hexanucleotide primers dna labelling megaprime kit/product/Amersham Life Sciences Inc
Average 90 stars, based on 1 article reviews
random sequence hexanucleotide primers dna labelling megaprime kit - by Bioz Stars, 2026-03
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Image Search Results


Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random hexanucleotides (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.

Journal:

Article Title: Distribution of acetylated histones resulting from Gal4-VP16 recruitment of SAGA and NuA4 complexes

doi: 10.1093/emboj/19.11.2629

Figure Lengend Snippet: Fig. 5. Gal4-VP16 directs the HAT activity of the SAGA complex to promoter-proximal nucleosomes. The experimental set-up for these ‘scanning ChIPS’ is similar to that used in Figure ​Figure4:4: the template was incubated in the absence (–) or presence (+) of Gal4-VP16, and competitor chromatin was added where indicated. Next, the reactions were incubated with SAGA and acetyl-CoA (or mock acetylated in the absence of HAT complex), MNase digested and immunoprecipitated with anti-acetylated H3 antibody. DNA was extracted from the bound and unbound fractions and slot-blotted. The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random hexanucleotides (Boehringer Mannheim). (A) Diagram showing the localization of the different probes when the plasmid is digested with BglI. (B) Average values and standard deviation of normalized data from three repeats of the experiment. The background signal (–HAT) was subtracted from the values obtained in the presence of SAGA for each condition. The numbers under the graph show the ratio of proximal (average of +A and –A) versus distal (average of +C and –C) signal for each condition tested. ND, not determined. (C) The reconstituted array was pre-incubated with Gal4-VP16 and competitor chromatin was added. Then, the template was acetylated by SAGA in the presence of acetyl-CoA, reactions were digested with MNase (+) or mock-digested (–), and the immunoprecipitation and slot blot were carried out as described above.

Article Snippet: The membranes were hybridized successively with a series of short probes (between 250 and 300 bp) that scan the length of the template, generated by PCR and labeled by primer extension from random hexanucleotides (Boehringer Mannheim). ( A ) Diagram showing the localization of the different probes when the plasmid is digested with Bgl I. ( B ) Average values and standard deviation of normalized data from three repeats of the experiment.

Techniques: Activity Assay, Incubation, Immunoprecipitation, Generated, Labeling, Plasmid Preparation, Standard Deviation, Dot Blot