Expressing HA-tagged fusion protein, CMV promoter.
Alternative name | S-HA, single HA-tagged expression vector |
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Clone info. | Expression vector. Expressing HA-tagged fusion protein under the control of CMV promoter. |
Vector backbone | pRc/CMV (Plasmid) |
Size of vector backbone | 5.5 kb |
Selectable markers | Amp^r (E. coli), Neo^r (mammalian cell) |
Growth conditions | 37 C, LB+Amp |
Depositor|Developer | Takemoto, Yoshihiro | Hashimoto, Yasuhiro | Furuta, Masaaki | Sato, Mitsuru | |
Sequence | RDB02136z.seq |
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Additional map | ![]() |
Remarks, protocol and/or map (pdf) | RDB02136.pdf |
Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
Ordering forms | Order form [Credit Card Payment ![]() ![]() ![]() MTA, for use for not-for-profit academic purpose [Word ![]() ![]() Please visit Information of Request for Distribution.[link] For for-profit-research purpose, please contact us. |
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Terms and conditions for distribution | In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature(s) designated by the DEPOSITOR is requested (DNA Cell Biol., 16, 893-896 (1997)). |
必要書類 | 提供依頼書 ![]() ![]() 提供同意書 (MTA, 非営利学術目的用)[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。営利目的利用についてはお問い合わせください。 |
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MTAに書く使用条件 | 利用者は、研究成果の公表にあたって寄託者の指定する文献を引用する (DNA Cell Biol., 16, 893-896 (1997))。 |
Catalog # | Resource name | Shipping form | Fee (non-profit org.) |
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RDB02136 | S-HA-pRc/CMV | DNA solution |
JPY 9,460 (not-for-profit academic purpose) plus cost of shipping containers, dry ice (if required) and shipping charge |
Materials & Methods section:
The S-HA-pRc/CMV was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB02136). |
Reference section:
Takemoto, Y., Sato, M., Furuta, M., Hashimoto, Y., Expression plasmid vectors with convenient subcloning sites in lambda gt11 that efficiently produce detectable tagged proteins. DNA Cell Biol., 16, 893-896 (1997). PMID 9260932. [link to RRC of NBRP] |
Further references such as user reports and related articles (go to bottom)
RIKEN BRC has sequenced portions of this material for quality test.
Please review the QC test results indicated by icon as well as clone information before placing your order.
Test sheet | RDB13988_A6Cmp1.pdf ![]() |
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Nucleotide sequence of a portion of this resource (if available).
Primer: CMV_Forward (Pr0016) Region: CMV pro,T7 pro,HA,SP6 pro,bGH pA,M13 ori Sequence file: RDB13988_A6Cma.seq ![]() |
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>02136_13988_A6Cm_2_CMV-Forward_A01_01.ab1 1 NNNNNNNNNN CNNTTGNNGC NNTGGGCGGT AGGCGTGTAC GGTGGGAGGT CTATATAAGC 61 AGAGCTCTCT GGCTAACTAG AGAACCCACT GCTTACTGGC TTATCGAAAT TAATACGACT 121 CACTATAGGG AGACCCAAGC TTCCATGGCC TACCCCTACG ACGTGCCCGA CTACGCCGCG 181 GCCGCTCGAG CATGCATCTA GAGGGCCCTA TTCTATAGTG TCACCTAAAT GCTAGAGCTC 241 GCTGATCAGC CTCGACTGTG CCTTCTAGTT GCCAGCCATC TGTTGTTTGC CCCTCCCCCG 301 TGCCTTCCTT GACCCTGGAA GGTGCCACTC CCACTGTCCT TTCCTAATAA AATGAGGAAA 361 TTGCATCGCA TTGTCTGAGT AGGTGTCATT CTATTCTGGG GGGTGGGGTG GGGCAGGACA 421 GCAAGGGGGA GGATTGGGAA GACAATAGCA GGCATGCTGG GGATGCGGTG GGCTCTATGG 481 CTTCTGAGGC GGAAAGAACC AGCTGGGGCT CGAGGGGGGA TCCCCACGCG CCCTGTAGCG 541 GCGCATTAAG CGCGGCGGGT GTGGTGGTTA CGCGCAGCGT GACCGCTACA CTTGCCAGCG 601 CCCTAGCGCC CGCTCCTTTC GCTTTCTTCC CTTCCTTTCT CGCCACGTTC GCCGGCTTTC 661 CCCGTCAAGC TCTAAATCGG GNGCTCCCTT TAGGGTTCCG ATTTAGTGCT TTACGGCACC 721 TCGACCCCNA AAAACTTGAN TANGGTGANG GNTCACGTAG TGGGNCATCG CCCNGATAGA 781 NGGNTTTTCG CCCTTTGACG TNNGANTNNN NNTTCTTNNN TANTGNNNTC NNGNNNNNAN 841 NTNNNNCNNC ACTCNNCCCT ATNNNNGNNN ANTCNTTTGA NTNATNNNGN ANTTNNNNNN 901 NTNNNNNNNN NN // |
Primer: SV40pro_F_V2 (Pr0154) Region: NeoR Sequence file: RDB13988_A6Cmb.seq ![]() |
>02136_13988_A6Cm_2_SV40pro_F_V2_B01_04.ab1 1 NNNNNNNNNN NNNNNNNNNN CNNNGCTTTT GCNNNNNNTC CCGGGNNCTT GGATATCCNT 61 TTTCGGATCT GATCAAGAGA CAGGATGAGG ATCGTTTCGC ATGATTGAAC AAGATGGATT 121 GCACGCAGGT TCTCCGGCCG CTTGGGTGGA GAGGCTATTC GGCTATGACT GGGCACAACA 181 GACAATCGGC TGCTCTGATG CCGCCGTGTT CCGGCTGTCA GCGCAGGGGC GCCCGGTTCT 241 TTTTGTCAAG ACCGACCTGT CCGGTGCCCT GAATGAACTG CAGGACGAGG CAGCGCGGCT 301 ATCGTGGCTG GCCACGACGG GCGTTCCTTG CGCAGCTGTG CTCGACGTTG TCACTGAAGC 361 GGGAAGGGAC TGGCTGCTAT TGGGCGAAGT GCCGGGGCAG GATCTCCTGT CATCTCACCT 421 TGCTCCTGCC GAGAAAGTAT CCATCATGGC TGATGCAATG CGGCGGCTGC ATACGCTTGA 481 TCCGGCTACC TGCCCATTCG ACCACCAAGC GAAACATCGC ATCGAGCGAG CACGTACTCG 541 GATGGAAGCC GGTCTTGTCG ATCAGGATGA TCTGGACGAA GAGCATCAGG GGCTCGCGCC 601 AGCCGAACTG TTCGCCAGGC TCAAGGCGCG CATGCCCGAC GGCGAGGATC TCGTCGTGAC 661 CCATGGCGAT GCCTGCTTGC CGAATATCAT GGTGGAAAAT GGCCGCTTTT CTGGATTCAT 721 CGACTGTGGC CGGCTGGGTG TGGCGGACCG CTATCAGGAC ATAGCGTTGG CTACCCGTGA 781 TATTGCTGAA GAGCTTGGCG GCGAATGGNC TGACCGCTTC CTCGTGCTTT ACGGTATCGC 841 CGCTCCCGAT TCNCAGCGCA TCGCCTTCTA TCGCCTTCTT GACGANTNCT TCTGNNCGGG 901 ANTCTGGGGG NTCGAAATGA CCGANNNAGC GACNCCCAAC CTGNCNTCAC NANANTTCGA 961 TNNCNNCNGN CGCCNTCTAT GAAANNNNGG GCNNNNGNNN NNTTTTNNNG GNNNNNNNNN 1021 N // |
Please visit Sequencing and PCR primers for primer information.
Original, user report and related articles
original | Takemoto, Y., Expression plasmid vectors with convenient subcloning sites in lambda gt11 that efficiently produce detectable tagged proteins. DNA Cell Biol., 16, 893-896 (1997). PMID 9260932. [link to RRC of NBRP] |
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