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Kentaro Miyazaki's Resource

Kentaro Miyazaki's web page in English /  in Japanese

Learn more about their research in Researchmap

Catalog #Name of cloneRunning titlePublication
RDB18374pUC18C_mPAG2Cloning vector harboring PheS counterselection marker. Chloramphenicol resistance.Miyazaki, K., Molecular engineering of a PheS counterselection marker for improved operating efficiency in Escherichia coli. Biotechniques 58 (2): 86-88 (2015). PMID 25652032. (reference). [link to RRC of NBRP]
RDB18373pUC18Z_mPAG2Cloning vector harboring PheS counterselection marker. Zeocin resistance.Miyazaki, K., Molecular engineering of a PheS counterselection marker for improved operating efficiency in Escherichia coli. Biotechniques 58 (2): 86-88 (2015). PMID 25652032. (reference). [link to RRC of NBRP]
RDB18372pUC18K_mPAG2Cloning vector harboring PheS counterselection marker. Kanamycin resistance. Miyazaki, K., Molecular engineering of a PheS counterselection marker for improved operating efficiency in Escherichia coli. Biotechniques 58 (2): 86-88 (2015). PMID 25652032. (reference). [link to RRC of NBRP]
RDB17948pUC18Z_ePAG2Cloning vector harboring counterselection marker Escherichia coli phenylalanyl-tRNA synthetase a-subunit (ePheS).Miyazaki, K., Molecular engineering of a PheS counterselection marker for improved operating efficiency in Escherichia coli. Biotechniques 58 (2): 86-88 (2015). PMID 25652032. (original). [link to RRC of NBRP]
RDB17947pUC18K_ePAG2Cloning vector harboring counterselection marker Escherichia coli phenylalanyl-tRNA synthetase a-subunit (ePheS).Miyazaki, K., Molecular engineering of a PheS counterselection marker for improved operating efficiency in Escherichia coli. Biotechniques 58 (2): 86-88 (2015). PMID 25652032. (original). [link to RRC of NBRP]
RDB17946pSAL7A35VSBacterial expression vector for the salicylate-inducible high expression system in E. coli.Miyazaki, K., Molecular engineering of the salicylate-inducible transcription factor Sal7AR for orthogonal and high gene expression in Escherichia coli. PLoS One 13 (4): e0194090 (2018). PMID 29641575. (original). [link to RRC of NBRP]
RDB17943pUC4KrB1Plasmid clone of T. thermophilus strain HB27 16S ribosomal RNA gene (rrsB) with its flanking regionsMiyazaki, K., Occurrence of randomly recombined functional 16S rRNA genes in Thermus thermophilus suggests genetic interoperability and promiscuity of bacterial 16S rRNAs. Sci. Rep. 9 (1): 11233 (2019). PMID 31375780. (original). [link to RRC of NBRP]

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No Approval Forms Required for Fluorescent Protein Genes Developed by Dr. Atsushi Miyawaki
♦ RIKEN BRC will be closed from December 28, 2024 through January 5, 2025 due to New Year's holidays.
A bicistronic cell cycle reporter, Fucci2a (Sep 17, 2024)
Monomeric Fluorescent Protein Resource, mStayGold (Dec 18, 2023)
Visualization of Organelles update (Dec 18, 2023)
Development of two mouse strains conditionally expressing bright luciferases (Sep 08, 2023)
Autophagy and Mitophagy Updates (Aug 16, 2023)
High intensity forms of luciferase and luminescent proteins from various organisms (BRC RESOURCE NEWS) (Apr 28, 2023)
Plasmid of Cas9 expression/mRNA production, evaluation of the genome edit efficiency, and Knock-in donors and tags
Fucci cell cycle indicator, Calcium sensor and Fluorescent and Luminescent protein resources
Revision of Distribution Fees for Bioresources in RIKEN BRC
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2025.03.24

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