low-input quick amp single color labeling kit (Agilent technologies)
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low-input quick amp single color labeling kit
Low Input Quick Amp Single Color Labeling Kit, supplied by Agilent technologies, 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/product/low-input+quick+amp+labeling+kit/pmc11310327-332-12-11
Average 90 stars, based on 1 article reviews
Low Input Quick Amp Single Color Labeling Kit, supplied by Agilent technologies, 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/product/low-input+quick+amp+labeling+kit/pmc11310327-332-12-11
Average 90 stars, based on 1 article reviews
low-input quick amp single color labeling kit - by Bioz Stars,
2026-09
90/100 stars
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Labeling:Article Title: Human Adult Renal Progenitor Cells Prevent Cisplatin-Nephrotoxicity by Inducing CYP1B1 Overexpression and miR-27b-3p Down-Regulation through Extracellular Vesicles. Article Snippet: The total RNA samples were then mixed with diluted RNA spike-in controls and labelled with Article Title: The embryo affects day 14 uterine transcriptome depending on nutritional status in sheep. a. Metabolic adaptation to pregnancy in nourished and undernourished ewes. Article Snippet: Briefly, a 148 total of 200 ng of RNA per sample (or Article Title: Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice Article Snippet: Cy3-labeled cRNA was prepared from 200 ng of total Article Title: Relative Contributions of Extracellular and Internalized Bacteria to Early Macrophage Proinflammatory Responses to Streptococcus pneumoniae Article Snippet: An Article Title: Inhibition of GSK-3β Enhances Osteoblast Differentiation of Human Mesenchymal Stem Cells through Wnt Signalling Overexpressing Runx2. Article Snippet: An amount of 200 ng of total Article Title: Myeloid Slc2a1 -Deficient Murine Model Revealed Macrophage Activation and Metabolic Phenotype Are Fueled by GLUT1 Article Snippet: Samples (2 μl) were Article Title: Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals. Article Snippet: Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ixen20 Xenobiotica the fate of foreign compounds in biological systems ISSN: 0049-8254 (Print) 1366-5928 (Online) Journal homepage: https://www.tandfonline.com/loi/ixen20 Identification of gene expression markers and development of evaluation method using cellbased and RT-PCR-based assay for skin sensitising potential of chemicals Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose To cite this article: Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose (2020): Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals, Xenobiotica, DOI: 10.1080/00498254.2020.1767320 To link to this article: https://doi.org/10.1080/00498254.2020.1767320 Accepted author version posted online: 12 May 2020.. Submit your article to this journal View related articles View Crossmark data Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers Maho Ukaji Nishikawa, 1 Megumi Iwaki, 1 Kosuke Tashiro, 2 Kouichi Kurose 1* 1 Department of Food Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan 2 Division of Molecular Biosciences, Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan *Corresponding author: Address for correspondence: Dr. Kouichi Kurose, Department of Food Science and Technology, Tokyo University of Marine Science and Technology, 4-5-7 Konan, Minato-ku, Tokyo, 108-8477, Japan.. E-mail: kkuros0@kaiyodai.ac.jp Ac ce pt ed M an us rip t Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers 1. Article Title: A 22-gene transcriptomic model indicating individual therapy durations in multidrug-resistant tuberculosis Article Snippet: Total RNA was used for reverse transcription and subsequent Cy3-labelling with the Low-Input Quick Amp Labeling Kit (Agilent®, Böblingen, Germany) according to the One-Color Microarray-Based Gene Expression Analysis Protocol version 6.9.1 ( Microarray:Article Title: Human Adult Renal Progenitor Cells Prevent Cisplatin-Nephrotoxicity by Inducing CYP1B1 Overexpression and miR-27b-3p Down-Regulation through Extracellular Vesicles. Article Snippet: The total RNA samples were then mixed with diluted RNA spike-in controls and labelled with Article Title: The embryo affects day 14 uterine transcriptome depending on nutritional status in sheep. a. Metabolic adaptation to pregnancy in nourished and undernourished ewes. Article Snippet: Briefly, a 148 total of 200 ng of RNA per sample (or Article Title: Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice Article Snippet: Cy3-labeled cRNA was prepared from 200 ng of total Article Title: Relative Contributions of Extracellular and Internalized Bacteria to Early Macrophage Proinflammatory Responses to Streptococcus pneumoniae Article Snippet: An Article Title: Inhibition of GSK-3β Enhances Osteoblast Differentiation of Human Mesenchymal Stem Cells through Wnt Signalling Overexpressing Runx2. Article Snippet: An amount of 200 ng of total Article Title: Myeloid Slc2a1 -Deficient Murine Model Revealed Macrophage Activation and Metabolic Phenotype Are Fueled by GLUT1 Article Snippet: Samples (2 μl) were Article Title: Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals. Article Snippet: Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ixen20 Xenobiotica the fate of foreign compounds in biological systems ISSN: 0049-8254 (Print) 1366-5928 (Online) Journal homepage: https://www.tandfonline.com/loi/ixen20 Identification of gene expression markers and development of evaluation method using cellbased and RT-PCR-based assay for skin sensitising potential of chemicals Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose To cite this article: Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose (2020): Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals, Xenobiotica, DOI: 10.1080/00498254.2020.1767320 To link to this article: https://doi.org/10.1080/00498254.2020.1767320 Accepted author version posted online: 12 May 2020.. Submit your article to this journal View related articles View Crossmark data Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers Maho Ukaji Nishikawa, 1 Megumi Iwaki, 1 Kosuke Tashiro, 2 Kouichi Kurose 1* 1 Department of Food Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan 2 Division of Molecular Biosciences, Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan *Corresponding author: Address for correspondence: Dr. Kouichi Kurose, Department of Food Science and Technology, Tokyo University of Marine Science and Technology, 4-5-7 Konan, Minato-ku, Tokyo, 108-8477, Japan.. E-mail: kkuros0@kaiyodai.ac.jp Ac ce pt ed M an us rip t Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers 1. Article Title: A 22-gene transcriptomic model indicating individual therapy durations in multidrug-resistant tuberculosis Article Snippet: Total RNA was used for reverse transcription and subsequent Cy3-labelling with the Low-Input Quick Amp Labeling Kit (Agilent®, Böblingen, Germany) according to the One-Color Microarray-Based Gene Expression Analysis Protocol version 6.9.1 ( Purification:Article Title: Human Adult Renal Progenitor Cells Prevent Cisplatin-Nephrotoxicity by Inducing CYP1B1 Overexpression and miR-27b-3p Down-Regulation through Extracellular Vesicles. Article Snippet: The total RNA samples were then mixed with diluted RNA spike-in controls and labelled with Article Title: The embryo affects day 14 uterine transcriptome depending on nutritional status in sheep. a. Metabolic adaptation to pregnancy in nourished and undernourished ewes. Article Snippet: Briefly, a 148 total of 200 ng of RNA per sample (or Article Title: Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice Article Snippet: Cy3-labeled cRNA was prepared from 200 ng of total Article Title: Relative Contributions of Extracellular and Internalized Bacteria to Early Macrophage Proinflammatory Responses to Streptococcus pneumoniae Article Snippet: An Article Title: Inhibition of GSK-3β Enhances Osteoblast Differentiation of Human Mesenchymal Stem Cells through Wnt Signalling Overexpressing Runx2. Article Snippet: An amount of 200 ng of total Article Title: Myeloid Slc2a1 -Deficient Murine Model Revealed Macrophage Activation and Metabolic Phenotype Are Fueled by GLUT1 Article Snippet: Samples (2 μl) were Article Title: Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals. Article Snippet: Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ixen20 Xenobiotica the fate of foreign compounds in biological systems ISSN: 0049-8254 (Print) 1366-5928 (Online) Journal homepage: https://www.tandfonline.com/loi/ixen20 Identification of gene expression markers and development of evaluation method using cellbased and RT-PCR-based assay for skin sensitising potential of chemicals Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose To cite this article: Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose (2020): Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals, Xenobiotica, DOI: 10.1080/00498254.2020.1767320 To link to this article: https://doi.org/10.1080/00498254.2020.1767320 Accepted author version posted online: 12 May 2020.. Submit your article to this journal View related articles View Crossmark data Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers Maho Ukaji Nishikawa, 1 Megumi Iwaki, 1 Kosuke Tashiro, 2 Kouichi Kurose 1* 1 Department of Food Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan 2 Division of Molecular Biosciences, Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan *Corresponding author: Address for correspondence: Dr. Kouichi Kurose, Department of Food Science and Technology, Tokyo University of Marine Science and Technology, 4-5-7 Konan, Minato-ku, Tokyo, 108-8477, Japan.. E-mail: kkuros0@kaiyodai.ac.jp Ac ce pt ed M an us rip t Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers 1. Article Title: A 22-gene transcriptomic model indicating individual therapy durations in multidrug-resistant tuberculosis Article Snippet: Total RNA was used for reverse transcription and subsequent Cy3-labelling with the Low-Input Quick Amp Labeling Kit (Agilent®, Böblingen, Germany) according to the One-Color Microarray-Based Gene Expression Analysis Protocol version 6.9.1 ( Amplification:Article Title: Human Adult Renal Progenitor Cells Prevent Cisplatin-Nephrotoxicity by Inducing CYP1B1 Overexpression and miR-27b-3p Down-Regulation through Extracellular Vesicles. Article Snippet: The total RNA samples were then mixed with diluted RNA spike-in controls and labelled with Article Title: The embryo affects day 14 uterine transcriptome depending on nutritional status in sheep. a. Metabolic adaptation to pregnancy in nourished and undernourished ewes. Article Snippet: Briefly, a 148 total of 200 ng of RNA per sample (or Article Title: Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice Article Snippet: Cy3-labeled cRNA was prepared from 200 ng of total Article Title: Relative Contributions of Extracellular and Internalized Bacteria to Early Macrophage Proinflammatory Responses to Streptococcus pneumoniae Article Snippet: An Article Title: Inhibition of GSK-3β Enhances Osteoblast Differentiation of Human Mesenchymal Stem Cells through Wnt Signalling Overexpressing Runx2. Article Snippet: An amount of 200 ng of total Article Title: Myeloid Slc2a1 -Deficient Murine Model Revealed Macrophage Activation and Metabolic Phenotype Are Fueled by GLUT1 Article Snippet: Samples (2 μl) were Article Title: Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals. Article Snippet: Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ixen20 Xenobiotica the fate of foreign compounds in biological systems ISSN: 0049-8254 (Print) 1366-5928 (Online) Journal homepage: https://www.tandfonline.com/loi/ixen20 Identification of gene expression markers and development of evaluation method using cellbased and RT-PCR-based assay for skin sensitising potential of chemicals Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose To cite this article: Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose (2020): Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals, Xenobiotica, DOI: 10.1080/00498254.2020.1767320 To link to this article: https://doi.org/10.1080/00498254.2020.1767320 Accepted author version posted online: 12 May 2020.. Submit your article to this journal View related articles View Crossmark data Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers Maho Ukaji Nishikawa, 1 Megumi Iwaki, 1 Kosuke Tashiro, 2 Kouichi Kurose 1* 1 Department of Food Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan 2 Division of Molecular Biosciences, Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan *Corresponding author: Address for correspondence: Dr. Kouichi Kurose, Department of Food Science and Technology, Tokyo University of Marine Science and Technology, 4-5-7 Konan, Minato-ku, Tokyo, 108-8477, Japan.. E-mail: kkuros0@kaiyodai.ac.jp Ac ce pt ed M an us rip t Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers 1. Article Title: A 22-gene transcriptomic model indicating individual therapy durations in multidrug-resistant tuberculosis Article Snippet: Total RNA was used for reverse transcription and subsequent Cy3-labelling with the Low-Input Quick Amp Labeling Kit (Agilent®, Böblingen, Germany) according to the One-Color Microarray-Based Gene Expression Analysis Protocol version 6.9.1 ( Expressing:Article Title: Human Adult Renal Progenitor Cells Prevent Cisplatin-Nephrotoxicity by Inducing CYP1B1 Overexpression and miR-27b-3p Down-Regulation through Extracellular Vesicles. Article Snippet: The total RNA samples were then mixed with diluted RNA spike-in controls and labelled with Article Title: The embryo affects day 14 uterine transcriptome depending on nutritional status in sheep. a. Metabolic adaptation to pregnancy in nourished and undernourished ewes. Article Snippet: Briefly, a 148 total of 200 ng of RNA per sample (or Article Title: Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice Article Snippet: Cy3-labeled cRNA was prepared from 200 ng of total Article Title: Relative Contributions of Extracellular and Internalized Bacteria to Early Macrophage Proinflammatory Responses to Streptococcus pneumoniae Article Snippet: An Article Title: Inhibition of GSK-3β Enhances Osteoblast Differentiation of Human Mesenchymal Stem Cells through Wnt Signalling Overexpressing Runx2. Article Snippet: An amount of 200 ng of total Article Title: Myeloid Slc2a1 -Deficient Murine Model Revealed Macrophage Activation and Metabolic Phenotype Are Fueled by GLUT1 Article Snippet: Samples (2 μl) were Article Title: Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals. Article Snippet: Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=ixen20 Xenobiotica the fate of foreign compounds in biological systems ISSN: 0049-8254 (Print) 1366-5928 (Online) Journal homepage: https://www.tandfonline.com/loi/ixen20 Identification of gene expression markers and development of evaluation method using cellbased and RT-PCR-based assay for skin sensitising potential of chemicals Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose To cite this article: Maho Ukaji Nishikawa, Megumi Iwaki, Kosuke Tashiro & Kouichi Kurose (2020): Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals, Xenobiotica, DOI: 10.1080/00498254.2020.1767320 To link to this article: https://doi.org/10.1080/00498254.2020.1767320 Accepted author version posted online: 12 May 2020.. Submit your article to this journal View related articles View Crossmark data Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers Maho Ukaji Nishikawa, 1 Megumi Iwaki, 1 Kosuke Tashiro, 2 Kouichi Kurose 1* 1 Department of Food Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan 2 Division of Molecular Biosciences, Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan *Corresponding author: Address for correspondence: Dr. Kouichi Kurose, Department of Food Science and Technology, Tokyo University of Marine Science and Technology, 4-5-7 Konan, Minato-ku, Tokyo, 108-8477, Japan.. E-mail: kkuros0@kaiyodai.ac.jp Ac ce pt ed M an us rip t Identification of gene expression markers and development of evaluation method using cell-based and RT-PCR-based assay for skin sensitising potential of chemicals Running Head: A new evaluation method for skin sensitisers 1. Article Title: A 22-gene transcriptomic model indicating individual therapy durations in multidrug-resistant tuberculosis Article Snippet: Total RNA was used for reverse transcription and subsequent Cy3-labelling with the Low-Input Quick Amp Labeling Kit (Agilent®, Böblingen, Germany) according to the One-Color Microarray-Based Gene Expression Analysis Protocol version 6.9.1 ( |