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random primer dna labeling kit ver  (TaKaRa)


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    Structured Review

    TaKaRa random primer dna labeling kit ver
    Random Primer Dna Labeling Kit Ver, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 6513 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/random+primer+dna+labeling+kit+ver/Random+Primer/pmc12944927-62-25-31
    Average 96 stars, based on 6513 article reviews
    random primer dna labeling kit ver - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Purification:

    Article Title: Fabrication and evaluation of agarose-curdlan blend derived multifunctional nanofibrous mats for diabetic wounds.
    Article Snippet: Grapevine red blotch virus (GRBV) is the causative agent of grapevine red blotch disease (GRBD) which is one of the major threats faced by grapevine industry in the United States.. Since its initial identification in 2011, the disease has rapidly spread in the major US grape-growing regions of the Pacific Northwest, causing major economic impacts.. Geminiviruses, the largest family of plant viruses, can induce and be targeted by host post-transcriptional gene-silencing (PTGS) anti-viral mechanisms.

    Article Title: Replication fork blocking deficiency leads to a reduction of rDNA copy number in budding yeast
    Article Snippet: .. Probes were amplified with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa), and purified by ProbeQuant G-50 Micro Columns (GE Healthcare). ..

    Random Primer DNA Labeling:

    Article Title: Fabrication and evaluation of agarose-curdlan blend derived multifunctional nanofibrous mats for diabetic wounds.
    Article Snippet: Grapevine red blotch virus (GRBV) is the causative agent of grapevine red blotch disease (GRBD) which is one of the major threats faced by grapevine industry in the United States.. Since its initial identification in 2011, the disease has rapidly spread in the major US grape-growing regions of the Pacific Northwest, causing major economic impacts.. Geminiviruses, the largest family of plant viruses, can induce and be targeted by host post-transcriptional gene-silencing (PTGS) anti-viral mechanisms.

    Article Title: ERC accumulation depletes Sir2 from rDNA and induces cellular senescence by rDNA destabilization
    Article Snippet: .. The PCR product was gel-purified, and 50 ng was used for random priming reactions in the presence of the radiolabeled nucleotide, [α- 32 P]dCTP (3000 Ci/mmol, 10 mCi/ml, PerkinElmer), using the Random Primer DNA Labeling Kit Ver.2 (TaKaRa). .. Unincorporated nucleotides were removed using ProbeQuant G-50 Micro Columns (GE Healthcare).

    Article Title: ERC accumulation depletes Sir2 from rDNA and induces cellular senescence by rDNA destabilization.
    Article Snippet: .. The PCR product was gel-purified, and 50 ng was used for random priming reactions in the presence of the radiolabeled nucleotide, [ α- 32 P]dCTP (3000 Ci / mmol, 10 mCi / ml, PerkinElmer), using the Random Primer DNA Labeling Kit Ver.2 (TaKaRa). .. Unincorporated nucleotides were removed using ProbeQuant G-50 Micro Columns (GE Healthcare).

    Article Title: Development of a Novel Human Hepatoma Cell Line Supporting the Replication of a Recombinant HBV Genome with a Reporter Gene
    Article Snippet: .. The membrane was immobilized using an ultraviolet crosslinker and hybridized with a P32-α-dCTP-labeled full-length HBV-DNA fragment probe (GenBank accession number AB246345 ) generated with a Random Primer DNA Labeling Kit Ver.2 (Takara Bio). .. Detection was performed with a BAS Imaging Plate (BAS IP MS 2025 E; Cytiva) and analyzed using a Typhoon FLA7000 scanner (Cytiva).

    Article Title: Development of a Novel Human Hepatoma Cell Line Supporting the Replication of a Recombinant HBV Genome with a Reporter Gene
    Article Snippet: .. The membrane was immobilized using an ultraviolet crosslinker and hybridized with a P32-α-dCTP-labeled full-length HBV-DNA fragment probe (GenBank accession number AB246345) generated with a Random Primer DNA Labeling Kit Ver.2 (Takara Bio). .. Detection was performed with a BAS Imaging Plate (BAS IP MS 2025 E; Cytiva) and analyzed using a Typhoon FLA7000 scanner (Cytiva).

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA.
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N+; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α-32P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Article Title: Replication fork blocking deficiency leads to a reduction of rDNA copy number in budding yeast
    Article Snippet: .. Probes were amplified with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa), and purified by ProbeQuant G-50 Micro Columns (GE Healthcare). ..

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N + ; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α- 32 P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Polymerase Chain Reaction:

    Article Title: ERC accumulation depletes Sir2 from rDNA and induces cellular senescence by rDNA destabilization
    Article Snippet: .. The PCR product was gel-purified, and 50 ng was used for random priming reactions in the presence of the radiolabeled nucleotide, [α- 32 P]dCTP (3000 Ci/mmol, 10 mCi/ml, PerkinElmer), using the Random Primer DNA Labeling Kit Ver.2 (TaKaRa). .. Unincorporated nucleotides were removed using ProbeQuant G-50 Micro Columns (GE Healthcare).

    Article Title: ERC accumulation depletes Sir2 from rDNA and induces cellular senescence by rDNA destabilization.
    Article Snippet: .. The PCR product was gel-purified, and 50 ng was used for random priming reactions in the presence of the radiolabeled nucleotide, [ α- 32 P]dCTP (3000 Ci / mmol, 10 mCi / ml, PerkinElmer), using the Random Primer DNA Labeling Kit Ver.2 (TaKaRa). .. Unincorporated nucleotides were removed using ProbeQuant G-50 Micro Columns (GE Healthcare).

    Membrane:

    Article Title: Development of a Novel Human Hepatoma Cell Line Supporting the Replication of a Recombinant HBV Genome with a Reporter Gene
    Article Snippet: .. The membrane was immobilized using an ultraviolet crosslinker and hybridized with a P32-α-dCTP-labeled full-length HBV-DNA fragment probe (GenBank accession number AB246345 ) generated with a Random Primer DNA Labeling Kit Ver.2 (Takara Bio). .. Detection was performed with a BAS Imaging Plate (BAS IP MS 2025 E; Cytiva) and analyzed using a Typhoon FLA7000 scanner (Cytiva).

    Article Title: Development of a Novel Human Hepatoma Cell Line Supporting the Replication of a Recombinant HBV Genome with a Reporter Gene
    Article Snippet: .. The membrane was immobilized using an ultraviolet crosslinker and hybridized with a P32-α-dCTP-labeled full-length HBV-DNA fragment probe (GenBank accession number AB246345) generated with a Random Primer DNA Labeling Kit Ver.2 (Takara Bio). .. Detection was performed with a BAS Imaging Plate (BAS IP MS 2025 E; Cytiva) and analyzed using a Typhoon FLA7000 scanner (Cytiva).

    Generated:

    Article Title: Development of a Novel Human Hepatoma Cell Line Supporting the Replication of a Recombinant HBV Genome with a Reporter Gene
    Article Snippet: .. The membrane was immobilized using an ultraviolet crosslinker and hybridized with a P32-α-dCTP-labeled full-length HBV-DNA fragment probe (GenBank accession number AB246345 ) generated with a Random Primer DNA Labeling Kit Ver.2 (Takara Bio). .. Detection was performed with a BAS Imaging Plate (BAS IP MS 2025 E; Cytiva) and analyzed using a Typhoon FLA7000 scanner (Cytiva).

    Article Title: Development of a Novel Human Hepatoma Cell Line Supporting the Replication of a Recombinant HBV Genome with a Reporter Gene
    Article Snippet: .. The membrane was immobilized using an ultraviolet crosslinker and hybridized with a P32-α-dCTP-labeled full-length HBV-DNA fragment probe (GenBank accession number AB246345) generated with a Random Primer DNA Labeling Kit Ver.2 (Takara Bio). .. Detection was performed with a BAS Imaging Plate (BAS IP MS 2025 E; Cytiva) and analyzed using a Typhoon FLA7000 scanner (Cytiva).

    Northern Blot:

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA.
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N+; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α-32P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N + ; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α- 32 P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Hybridization:

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA.
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N+; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α-32P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N + ; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α- 32 P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Labeling:

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA.
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N+; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α-32P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Article Title: TEFM facilitates transition from RNA synthesis to DNA synthesis at H-strand replication origin of mtDNA
    Article Snippet: The RNA was then transferred to nylon membranes (Hybond N + ; GE Healthcare) and UV-crosslinked. .. Detection of mitochondrial rRNAs and mRNAs and GAPDH mRNA was carried out via Northern hybridization using DNA probes labeled with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa) and [α- 32 P] dCTP (3000 Ci/mmol; PerkinElmer). ..

    Amplification:

    Article Title: Replication fork blocking deficiency leads to a reduction of rDNA copy number in budding yeast
    Article Snippet: .. Probes were amplified with the Random Primer DNA Labeling Kit Ver.2 (TaKaRa), and purified by ProbeQuant G-50 Micro Columns (GE Healthcare). ..



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