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Please review the QC test results indicated by check icon below as well as clone information before placing your order.

pPmatLuc1 (#RDB14359)

Luciferase of Pyrocoelia matsumurai firefly with higher luminous intensity.

Clone info. Luciferase of Pyrocoelia matsumurai firefly with higher luminous intensity. pPmatLuc1 is not expression vector. When the luciferase is expressed in any cells, the cDNA must be transferred to appropriate expression vectors by your own.
Vector backbone pUC19 (Plasmid)
Size of vector backbone 2.7 kb
Selectable markers Amp^r
Growth conditions LB+Amp, 37oC
Gene/insert name Pyrocoelia matsumurai Luciferase cDNA
Depositor|Developer OLYMPUS CORPORATION, | Ogoh, Katsunori |
 

Distribution information

Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
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Order form [Credit Card Payment] [Bank Transfer Payment] [Example of order form ]
MTA, for use for not-for-profit academic purpose [Word] [Example of MTA ]
MTA, for use for for-profit purpose [Word]
Please visit Information of Request for Distribution.[link] 
Terms and conditions for distribution In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the literature designated by the DEPOSITOR is requested (Akiyoshi R, Ogoh K, Suzuki H. 2012. Firefly luciferase. Japan patent publication 2012-235756). RECIPIENT must contact the OLYMPUS CORPORATION in the case of application for any patents or commercial use(*) based on the results from the use of the BIOLOGICAL RESOURCE. (*)Commercial use shall include: (1) incorporation of the BIOLOGICAL RESOURCE into products for sale; (2) the use of to the BIOLOGICAL RESOURCE for screening candidate compounds; (3) the use of to the BIOLOGICAL RESOURCE for quality control. The RECIPIENT of any organization including for-profit or nonprofit organizations may intend to use the BIOLOGICAL RESOURCE for basic researches with such purposes.
提供案内 (日本国内) [open/close]

必要書類
提供依頼書  [依頼書の記入例 ]
提供同意書 (MTA, 非営利学術目的用)[Word] [MTAの記入例 ]
提供同意書 (MTA, 営利目的用)[Word]
手続きの概要は、「提供申込みについて[link]」をご覧ください。
MTAに書く使用条件 利用者は、研究成果の公表にあたって別紙に定める寄託者の指定する文献を引用する (ホタル由来ルシフェラーゼ 特開2012-235756)。利用者が本件リソースを使用して得られた研究成果に基づき特許等の申請、及び商業活動(*)を行う場合は、オリンパス株式会社と別途協議を行う。(*)商用活動とは,本件リソースが製品の一部に組み込まれる場合,本件リソースを利用して製品となる候補物を探索または製品の品質管理を行う場合等とする。そのための基礎検討の使用に関しては,営利,非営利機関等の利用者制限は定めない。

Catalog # Resource name Shipping form Fee (non-profit org.)
RDB14359 pPmatLuc1 DNA solution JPY 9,460 (not-for-profit academic purpose)
JPY 18,920 (for-profit-research purpose)
plus cost of shipping containers, dry ice (if required) and shipping charge

Please review the QC test results indicated by check icon below as well as clone information before placing your order.

How to cite this biological resource

Materials & Methods section:

The pPmatLuc1 was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB14359).

Reference section:

Ogoh, K., Akiyoshi, R., Suzuki, H., Cloning and mutagenetic modification of the firefly luciferase gene and its use for bioluminescence microscopy of engrailed expression during Drosophila metamorphosis. Biochem. Biophys. Rep. 23: 100771 (2020). PMID 32490216. [link to RRC of NBRP]
Akiyoshi, R., Ogoh, K., Suzuki, H., Firefly luciferase. Japan Patent Abstracts 2012-235756. [link to RRC of NBRP]

Further references such as user reports and related articles (go to bottom)


QC test results

RIKEN BRC has sequenced portions of this material for quality test.
Please review the QC test results indicated by check icon as well as clone information before placing your order.

Test sheet RDB14359_A6Jcp1.pdf check

Nucleotide sequence of a portion of this resource (if available).

Primer: Reverse2
Sequence file: RDB14359_A6Jca.seq check
>D03707A1_A6Jc_2_Reverse2_B04_04_ABI24.ab1
    1 CATCATCATT ACGCCAGCTT GCATGCCTGC AGGTCGACTC TAGAGGATCC ACCATGGAAG
   61 ATGACCACAA GAACATCGTG CACGGCCCTG CCCCATTCTA CCCCCTGGAA GAGGGAACAG
  121 CCGGCGAGCA GCTGCACCGG GCCATGAAGA GATATGCCCA GGTGCCCGGC ACAATCGCCT
  181 TCACCGATGC CCACGTGGAA GTGAACATCA CCTACAGCGA GTACTTCGAG ATGGCCTGCC
  241 GGCTGGCCGA GACAATGAAG CGCTATGGCC TGGGCCTGCA GCACCACATT GCCGTGTGCA
  301 GCGAGAACAG CCTGCAGTTC TTCATGCCCG TGTGTGGCGC CCTGTTCATC GGAGTGGGAG
  361 TGGCCCCCAC CAACGACATC TACAACGAGA GAGAGCTGTA CAACAGCCTG AGCATCAGCC
  421 AGCCCACCAT CGTGTTCTGC AGCAAGCGGG CCCTGCAGAA AATCCTGGGC GTGCAGAAAA
  481 AGCTGCCCGT GATCGAGAAG ATCGTGATCC TGGACAGCCG CGAGGACTAC ATGGGCAAGC
  541 AGAGCATGTA CAGCTTCATC GAGAGCCATC TGCCCGCTGG CTTCAACGAG TACGACTACG
  601 TGCCCGACAC CTTCGACAGA GAGACAGCCA CCGCCCTGAT CATGAACAGC AGCGGCTCTA
  661 CCGGCCTGCC CAAGGGCGTG GAACTGACCC ACAAGAATGT GTGCGTGCGG TTCAGCCACT
  721 GCCGGGACCC TGTGTTCGGC AACCAGATCA TCCCCGACAC CGCTATCCTG ACCGTGATCC
  781 CCTTCCACCA CGGCTTCGGC ATGTTCACCA CCCTGGGCTA CCTGACCTGC GGCTTCCGGA
  841 TCGTGCTGAT GTACAGATTC GAGGAAGAAC TGTTCCTGCG GAGCCTGCAG GACTACAAGA
  901 TCCAGAGCGC CCTGCTGGTG CCTACCCTGT TCAGCTTCTT CGCCAAGAGC ACCCTGGTGG
  961 ATAAGTACGA CCTGAGCAAC CCTGCACGAG ATCGCCTCTG GGCGGAGCCC CCCCCTGGCT
 1021 AAGGAAGGTG GGAGAGCCCG TTGGTCAGCC GGATTCAAGC TGCCGTGGCA TCAGAACAGG
1081 ACTTACGTCT TGACCGAAGC ACAACCCGTC G
//
Primer: pUC-M13_-100
Sequence file: RDB14359_A6Jcb.seq check
>D03707A1_A6Jc_2_pUC-M13_-100_A04_01_ABI24.ab1
    1 GGCCTGTCAG GCCGATTAGT TGGGTACGCC AGGGTTTTCC CAGTCACGAC GTTGTAAAAC
   61 GACGGCCAGT GAATTCTCAC AGCTTGCTTT TCTTGCCCAT TGTCAGCATC TCGCGGATCT
  121 TCCGGCTGTC GATCTTGCCT GTCAGGCCCT TTGGCACCTC GTCCACGAAC TTCACGCCGC
  181 CTCTCAGCCT CTTGCTGGCG GTCACTTGTC CGGCCACGTA GTCCATCACT TCCTGCTCGG
  241 TCATGGTCTT GCCCTCTTCC AGCACCACCA CAGCGGCAGG CAGTTCGCCA GCATCAGCAT
  301 CAGGGATGCC GGCCACCCCG GCATCGAAGA TGAAGGGATG CTGCAGCAGG ATAGATTCCA
  361 GCTCGGCGGG TGGCACCTGG TAGCCCTGGT ACTTGATCAG GGACTTCAGC CGGTCCACGA
  421 TGAAGAAGTG GCCGTCCTTG TCGTAGTAGG CCAGGTCGCC AGAGTGCAGC CAGCCATCCT
  481 TGTCGATCAG GGCATTGGTG GCCTCGGGGT TGTTCACGTA GCCCTTCATA ATCATGGGGC
  541 CCTTCAGACA CAGCTCGCCC CTCTGGTTCA CGCCCAGTGT CTTGCTGGTG TCCAGGTCCA
  601 CAATCTTGGC GCTGAAAAAT GGGGCCACCT TTCCACAGGC GCCAGGCTTA TCGTCGCCCC
  661 TGGGGGTGAT GATCACGGCA GAGGTTGTCT CGGTCAGGCC GTAGCCCTGT CTGATGCCAG
  721 GCAGCTTGAA CCGCTTGGCC ACGGCCTCTC CCACTTCTTT AGCCAGGGGG GCTCCGCCAG
  781 AGGCGATCTC GTGCAGGTTG CTCAGGTCGT ACTTATCCAC CAGGGTGCTC TTGGCGAAGA
  841 AGCTGAACAG GGTAGGCACC AGCAGGGCGC TCTGGATCTT GTAGTCCTGC AGGCTCCGCA
  901 GGAACAGTTC TTCCTCGAAT CTGTACATCA GCACGATCCG GAAGCCGCAG TCAAGGTAGC
  961 CCAGGTGGTG AACATGCCGA AGCCGTGGGT GGAATGGGGA TCACGGGTCC AGGAATAGCG
 1021 GTGTCGGGGA TGATCTGGGA TTGCCGACAC ACGGTCCCGG CAGTGACCTG ATCGCACGCC
1081 ACAACATTCT TTGTTGGGTT CAAGT
//

Please visit Sequencing and PCR primers for primer information.


References

Original, user report and related articles

original Ogoh, K., Cloning and mutagenetic modification of the firefly luciferase gene and its use for bioluminescence microscopy of engrailed expression during Drosophila metamorphosis. Biochem. Biophys. Rep. 23: 100771 (2020). PMID 32490216. [link to RRC of NBRP]
original Akiyoshi, R., Firefly luciferase. Japan Patent Abstracts 2012-235756. [link to RRC of NBRP]
reference Nakashiba, T., Development of two mouse strains conditionally expressing bright luciferases with distinct emission spectra as new tools for in vivo imaging. Lab. Anim. (NY) 52 (10): 247-257 (2023). PMID 37679611. [link to RRC of NBRP]
review Suzuki, H., Bioluminescence microscopy for the visualization of gene expression patterns and the study of embryonic development. Proc. Arthropod. Embryol. Soc. Jpn. 53: 1-7 (2021).
user_report Yamamoto, K., In vivo imaging identified efficient antimicrobial treatment against Mycobacterium marinum infection in mouse footpads. Sci. Rep. 14 (1): 24343 (2024). PMID 39420066. [link to RRC of NBRP]