pGL4.39[luc2P/ATF6 RE/Hygro]载体

pGL4.39[luc2P/ATF6 RE/Hygro]载体

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    • 详细信息
    • 技术资料
    • 保存条件

      -20℃低温保存

    • 保质期

      三年

    • 英文名

      pGL4.39[luc2P/ATF6 RE/Hygro]

    • 库存

      20

    • 供应商

      泽叶生物

    pGL4.39载体基本信息

    出品公司: ZYbscience
    载体名称: pGL4.39
    质粒类型: 信号通路报告载体;哺乳动物载体;萤火虫荧光素酶报告载体
    高拷贝/低拷贝: --
    克隆方法: 限制性内切酶,多克隆位点
    启动子: Minimal Promotor
    载体大小: 6139 bp
    5' 测序引物及序列: --
    3' 测序引物及序列: --
    载体标签: luc2P
    载体抗性: 氨苄青霉素
    筛选标记: 潮霉素(Hygromycin)
    克隆菌株: TOP10等常规菌株
    宿主细胞(系): HEK293等
    备注: pGL4.39[luc2P/ATF6 RE/Hygro]载体是信号通路报告载体;含ATF6应答元件;含萤火虫荧光素酶报告基因luc2P。
    产品目录号: ZY3661
    稳定性: 稳表达
    组成型/诱导型: 组成型
    病毒/非病毒: 非病毒

    pGL4.39载体质粒图谱和多克隆位点信息

    pGL4.39载体图谱



    pGL4.39 载体特征

    pGL4.39载体简介

    The pGL4.39[luc2P/ATF6 RE/Hygro] Vector contains five copies of an ATF6 response element (ATF6 RE) that drives transcription of the luciferase reporter gene luc2P (Photinus pyralis). luc2P is a synthetically-derived luciferase sequence with humanized codon optimization that is designed for high expression and reduced anomalous transcription. The luc2P gene contains hPEST, a protein destabilization sequence, which allows luc2P protein levels to respond more quickly than those of luc2 to induction of transcription. The vector backbone contains an ampicillin resistance gene to allow selection in E. coli and a gene for hygromycin resistance to allow selection of stably transfected mammalian cell lines.
    
    Example Protocol
    In this example protocol, the pGL4.39[luc2P/ATF6 RE/Hygro] Vector is used to measure
    activation of the ATF6 RE in HeLa cells upon treatment with tunicamycin.. The pGL4.75
    Vector (encoding Renilla luciferase) is used as a normalization control. In designing such
    experiments, it is important that the chosen cell type can be transfected efficiently and
    that it expresses the proper components of the signaling pathway of interest in order to
    generate the biological response. Protocol optimization may be required for your particular
    cell type and assay conditions.
    
    实验材料
     DMEM (Life Technologies Cat.# 11995)
     Complete medium [DMEM supplemented with 10% fetal bovine serum (DMEM/FBS;
    Life Technologies Cat.# 16000] and 1X NEAA [Life Technologies Cat.# 11140])
     Dulbecco’s PBS (DPBS; Life Technologies Cat. # 14190)
     0.05% Tryspin-EDTA (Life Technologies Cat.# 25300)
     Charcoal-stripped FBS (Life Technologies Cat.# 126776-011)
     Opti-MEM I (Life Technologies Cat.# 31985)
     FuGENE HD Transfection Reagent (Cat.# E2311)
     Tunicamycin (Calbiochem Cat.# 654380)
     DMSO (Sigma Cat.# D2650)
     Dual-Glo Luciferase Assay System (Cat.# E2940)
     HeLa cells
     pGL4.75[hRluc/CMV] Vector (Cat.# E6931)
    
    实验流程
    Day 1: Reverse Transfection
    Preparation of Cells
    1. Grow HeLa cells in complete medium (DMEM + 10% FBS + 1X NEAA). Wash with
    DPBS and treat with one volume of 0.05% trypsin-EDTA. Resuspend cells in four
    volumes of complete medium.
    2. Pellet the cells by centrifugation at 200 × g for 5 minutes in a swinging-bucket rotor.
    Resuspend in complete medium at a concentration of 1 × 105 cells/ml.
    Preparation of Lipid:DNA Mixture
    1. Dilute pGL4.39[luc2P/ATF6 RE/Hygro] and pGL4.75 [hRluc/CMV] Renilla luciferase
    vector constructs in a 10:1 mass ratio, respectively, to 10ng total DNA/μl in Opti-
    MEM I.
    2. Add FuGENE HD to a 3:1 lipid:DNA ratio. Mix by pipetting. Incubate at room temperature
    for 30 minutes.
    3. Dilute lipid:DNA mixture 20-fold with 1 × 105 cells/ml cell suspension and mix by
    inversion.
    4. Plate 100μl per well into a solid, white 96-well plate (Corning Cat.# 3917).
    5. Incubate for 18 hours in a 37°C, 5% CO2 incubator.
    
    Day 2: Medium Replacement and Cell Treatment
    1. Resuspend tunicamycin to 10mM in DMSO. Serially dilute into DMSO to give
    1,000X stocks. Dilute 100-fold into DMEM to give 10X stocks.
    2. Remove existing medium from cells and replace with 72μl of DMEM + 0.5% charcoal-
    stripped FBS per well.
    3. Add 8μl of the 10X dilutions of tunicamycin and incubate for 18 hours in a 37°C,
    5% CO2 incubator.
    
    Day 3: Luminescence Measurement
    1. Remove plates from the 37°C, 5% CO2 incubator and allow to cool to room temperature
    for approximately 15 minutes.
    4. Add 80μl of the Dual-Glo Luciferase Assay System detection reagents and measure
    luminescence following the recommended protocol (Refer to the Dual-Glo
    Luciferase Assay System Technical Manual, #TM058 for details).
    
    

    pGL4.39载体序列

    LOCUS       JQ858519                6139 bp    DNA     circular SYN 02-JUL-2012
    DEFINITION  Reporter vector pGL4.39[luc2P/ATF6 RE/Hygro], complete sequence.
    ACCESSION   JQ858519
    VERSION     JQ858519.1  GI:392934106
    KEYWORDS    .
    SOURCE      Reporter vector pGL4.39[luc2P/ATF6 RE/Hygro]
      ORGANISM  Reporter vector pGL4.39[luc2P/ATF6 RE/Hygro]
                other sequences; artificial sequences; vectors.
    REFERENCE   1  (bases 1 to 6139)
      AUTHORS   McNamara,B.
      TITLE     Direct Submission
      JOURNAL   Submitted (29-MAR-2012) Scientific Communications, Promega
                Corporation, 2800 Woods Hollow Rd, Madison, WI 53711, USA
    FEATURES             Location/Qualifiers
         source          1..6139
                         /organism="Reporter vector pGL4.39[luc2P/ATF6 RE/Hygro]"
                         /mol_type="other DNA"
                         /db_xref="taxon:1203013"
         regulatory      105..258
                         /regulatory_class="terminator"
                         /note="transcriptional pause site"
         regulatory      105..153
                         /regulatory_class="polyA_signal_sequence"
                         /note="synthetic poly(A) signal sequence"
         primer_bind     207..226
                         /note="RVprimer3 binding site"
         regulatory      285..419
                         /regulatory_class="enhancer"
                         /note="ATF6 response element"
         regulatory      465..495
                         /regulatory_class="promoter"
                         /note="minP promoter"
         gene            528..2303
                         /gene="luc2P"
                         /note="synthetic luciferase"
         CDS             528..2303
                         /gene="luc2P"
                         /note="synthetic luciferase"
                         /codon_start=1
                         /transl_table=11
                         /product="luciferase"
                         /protein_id="AFM92245.1"
                         /db_xref="GI:392934108"
                         /translation="MEDAKNIKKGPAPFYPLEDGTAGEQLHKAMKRYALVPGTIAFTD
                         AHIEVDITYAEYFEMSVRLAEAMKRYGLNTNHRIVVCSENSLQFFMPVLGALFIGVAV
                         APANDIYNERELLNSMGISQPTVVFVSKKGLQKILNVQKKLPIIQKIIIMDSKTDYQG
                         FQSMYTFVTSHLPPGFNEYDFVPESFDRDKTIALIMNSSGSTGLPKGVALPHRTACVR
                         FSHARDPIFGNQIIPDTAILSVVPFHHGFGMFTTLGYLICGFRVVLMYRFEEELFLRS
                         LQDYKIQSALLVPTLFSFFAKSTLIDKYDLSNLHEIASGGAPLSKEVGEAVAKRFHLP
                         GIRQGYGLTETTSAILITPEGDDKPGAVGKVVPFFEAKVVDLDTGKTLGVNQRGELCV
                         RGPMIMSGYVNNPEATNALIDKDGWLHSGDIAYWDEDEHFFIVDRLKSLIKYKGYQVA
                         PAELESILLQHPNIFDAGVAGLPDDDAGELPAAVVVLEHGKTMTEKEIVDYVASQVTT
                         AKKLRGGVVFVDEVPKGLTGKLDARKIREILIKAKKGGKIAVNSHGFPPEVEEQAAGT
                         LPMSCAQESGMDRHPAACASARINV"
         regulatory      2343..2564
                         /regulatory_class="polyA_signal_sequence"
                         /note="SV40 late poly(A) signal"
         regulatory      2612..3030
                         /regulatory_class="enhancer"
                         /note="SV40 early enhancer/promoter"
         CDS             3055..4092
                         /note="hygromycin resistance"
                         /codon_start=1
                         /transl_table=11
                         /product="hygromycin phosphotransferase"
                         /protein_id="AFM92246.1"
                         /db_xref="GI:392934109"
                         /translation="MKKPELTATSVEKFLIEKFDSVSDLMQLSEGEESRAFSFDVGGR
                         GYVLRVNSCADGFYKDRYVYRHFASAALPIPEVLDIGEFSESLTYCISRRAQGVTLQD
                         LPETELPAVLQPVAEAMDAIAAADLSQTSGFGPFGPQGIGQYTTWRDFICAIADPHVY
                         HWQTVMDDTVSASVAQALDELMLWAEDCPEVRHLVHADFGSNNVLTDNGRITAVIDWS
                         EAMFGDSQYEVANIFFWRPWLACMEQQTRYFERRHPELAGSPRLRAYMLRIGLDQLYQ
                         SLVDGNFDDAAWAQGRCDAIVRSGAGTVGRTQIARRSAAVWTDGCVEVLADSGNRRPS
                         TRPRAKEVGRV"
         regulatory      4116..4164
                         /regulatory_class="polyA_signal_sequence"
                         /note="synthetic poly(A) signal sequence"
         primer_bind     complement(4231..4250)
                         /note="RVprimer4 binding site"
         rep_origin      4488..4524
         gene            complement(5279..6139)
                         /gene="bla"
                         /note="AmpR"
         CDS             complement(5279..6139)
                         /gene="bla"
                         /note="AmpR"
                         /codon_start=1
                         /transl_table=11
                         /product="beta-lactamase"
                         /protein_id="AFM92244.1"
                         /db_xref="GI:392934107"
                         /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGY
                         IELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVE
                         YSPVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRL
                         DRWEPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPL
                         LRSALPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIA
                         EIGASLIKHW"
    ORIGIN      
            1 actcgtcctt tttcaatatt attgaagcat ttatcagggt tactagtacg tctctcaagg
           61 ataagtaagt aatattaagg tacgggaggt attggacagg ccgcaataaa atatctttat
          121 tttcattaca tctgtgtgtt ggttttttgt gtgaatcgat agtactaaca tacgctctcc
          181 atcaaaacaa aacgaaacaa aacaaactag caaaataggc tgtccccagt gcaagtgcag
          241 gtgccagaac atttctctgg cctaactggc cggtacctga gctcatcgag acaggtgctg
          301 acgtggcatt catcgagaca ggtgctgacg tggcattcat cgagacaggt gctgacgtgg
          361 cattcatcga gacaggtgct gacgtggcat tcatcgagac aggtgctgac gtggcattcc
          421 tcgaggatat caagatctgg cctcggcggc caagcttaga cactagaggg tatataatgg
          481 aagctcgact tccagcttgg caatccggta ctgttggtaa agccaccatg gaagatgcca
          541 aaaacattaa gaagggccca gcgccattct acccactcga agacgggacc gccggcgagc
          601 agctgcacaa agccatgaag cgctacgccc tggtgcccgg caccatcgcc tttaccgacg
          661 cacatatcga ggtggacatt acctacgccg agtacttcga gatgagcgtt cggctggcag
          721 aagctatgaa gcgctatggg ctgaatacaa accatcggat cgtggtgtgc agcgagaata
          781 gcttgcagtt cttcatgccc gtgttgggtg ccctgttcat cggtgtggct gtggccccag
          841 ctaacgacat ctacaacgag cgcgagctgc tgaacagcat gggcatcagc cagcccaccg
          901 tcgtattcgt gagcaagaaa gggctgcaaa agatcctcaa cgtgcaaaag aagctaccga
          961 tcatacaaaa gatcatcatc atggatagca agaccgacta ccagggcttc caaagcatgt
         1021 acaccttcgt gacttcccat ttgccacccg gcttcaacga gtacgacttc gtgcccgaga
         1081 gcttcgaccg ggacaaaacc atcgccctga tcatgaacag tagtggcagt accggattgc
         1141 ccaagggcgt agccctaccg caccgcaccg cttgtgtccg attcagtcat gcccgcgacc
         1201 ccatcttcgg caaccagatc atccccgaca ccgctatcct cagcgtggtg ccatttcacc
         1261 acggcttcgg catgttcacc acgctgggct acttgatctg cggctttcgg gtcgtgctca
         1321 tgtaccgctt cgaggaggag ctattcttgc gcagcttgca agactataag attcaatctg
         1381 ccctgctggt gcccacacta tttagcttct tcgctaagag cactctcatc gacaagtacg
         1441 acctaagcaa cttgcacgag atcgccagcg gcggggcgcc gctcagcaag gaggtaggtg
         1501 aggccgtggc caaacgcttc cacctaccag gcatccgcca gggctacggc ctgacagaaa
         1561 caaccagcgc cattctgatc acccccgaag gggacgacaa gcctggcgca gtaggcaagg
         1621 tggtgccctt cttcgaggct aaggtggtgg acttggacac cggtaagaca ctgggtgtga
         1681 accagcgcgg cgagctgtgc gtccgtggcc ccatgatcat gagcggctac gttaacaacc
         1741 ccgaggctac aaacgctctc atcgacaagg acggctggct gcacagcggc gacatcgcct
         1801 actgggacga ggacgagcac ttcttcatcg tggaccggct gaagagcctg atcaaataca
         1861 agggctacca ggtagcccca gccgaactgg agagcatcct gctgcaacac cccaacatct
         1921 tcgacgccgg ggtcgccggc ctgcccgacg acgatgccgg cgagctgccc gccgcagtcg
         1981 tcgtgctgga acacggtaaa accatgaccg agaaggagat cgtggactat gtggccagcc
         2041 aggttacaac cgccaagaag ctgcgcggtg gtgttgtgtt cgtggacgag gtgcctaaag
         2101 gactgaccgg caagttggac gcccgcaaga tccgcgagat tctcattaag gccaagaagg
         2161 gcggcaagat cgccgtgaat tctcacggct tccctcccga ggtggaggag caggccgccg
         2221 gcaccctgcc catgagctgc gcccaggaga gcggcatgga tagacaccct gctgcttgcg
         2281 ccagcgccag gatcaacgtc taaggccgcg actctagagt cggggcggcc ggccgcttcg
         2341 agcagacatg ataagataca ttgatgagtt tggacaaacc acaactagaa tgcagtgaaa
         2401 aaaatgcttt atttgtgaaa tttgtgatgc tattgcttta tttgtaacca ttataagctg
         2461 caataaacaa gttaacaaca acaattgcat tcattttatg tttcaggttc agggggaggt
         2521 gtgggaggtt ttttaaagca agtaaaacct ctacaaatgt ggtaaaatcg ataaggatcc
         2581 gtttgcgtat tgggcgctct tccgctgatc tgcgcagcac catggcctga aataacctct
         2641 gaaagaggaa cttggttagc taccttctga ggcggaaaga accagctgtg gaatgtgtgt
         2701 cagttagggt gtggaaagtc cccaggctcc ccagcaggca gaagtatgca aagcatgcat
         2761 ctcaattagt cagcaaccag gtgtggaaag tccccaggct ccccagcagg cagaagtatg
         2821 caaagcatgc atctcaatta gtcagcaacc atagtcccgc ccctaactcc gcccatcccg
         2881 cccctaactc cgcccagttc cgcccattct ccgccccatg gctgactaat tttttttatt
         2941 tatgcagagg ccgaggccgc ctctgcctct gagctattcc agaagtagtg aggaggcttt
         3001 tttggaggcc taggcttttg caaaaagctc gattcttctg acactagcgc caccatgaag
         3061 aagcccgaac tcaccgctac cagcgttgaa aaatttctca tcgagaagtt cgacagtgtg
         3121 agcgacctga tgcagttgtc ggagggcgaa gagagccgag ccttcagctt cgatgtcggc
         3181 ggacgcggct atgtactgcg ggtgaatagc tgcgctgatg gcttctacaa agaccgctac
         3241 gtgtaccgcc acttcgccag cgctgcacta cccatccccg aagtgttgga catcggcgag
         3301 ttcagcgaga gcctgacata ctgcatcagt agacgcgccc aaggcgttac tctccaagac
         3361 ctccccgaaa cagagctgcc tgctgtgtta cagcctgtcg ccgaagctat ggatgctatt
         3421 gccgccgccg acctcagtca aaccagcggc ttcggcccat tcgggcccca aggcatcggc
         3481 cagtacacaa cctggcggga tttcatttgc gccattgctg atccccatgt ctaccactgg
         3541 cagaccgtga tggacgacac cgtgtccgcc agcgtagctc aagccctgga cgaactgatg
         3601 ctgtgggccg aagactgtcc cgaggtgcgc cacctcgtcc atgccgactt cggcagcaac
         3661 aacgtcctga ccgacaacgg ccgcatcacc gccgtaatcg actggtccga agctatgttc
         3721 ggggacagtc agtacgaggt ggccaacatc ttcttctggc ggccctggct ggcttgcatg
         3781 gagcagcaga ctcgctactt cgagcgccgg catcccgagc tggccggcag ccctcgtctg
         3841 cgagcctaca tgctgcgcat cggcctggat cagctctacc agagcctcgt ggacggcaac
         3901 ttcgacgatg ctgcctgggc tcaaggccgc tgcgatgcca tcgtccgcag cggggccggc
         3961 accgtcggtc gcacacaaat cgctcgccgg agcgcagccg tatggaccga cggctgcgtc
         4021 gaggtgctgg ccgacagcgg caaccgccgg cccagtacac gaccgcgcgc taaggaggta
         4081 ggtcgagttt aaactctaga accggtcatg gccgcaataa aatatcttta ttttcattac
         4141 atctgtgtgt tggttttttg tgtgttcgaa ctagatgctg tcgaccgatg cccttgagag
         4201 ccttcaaccc agtcagctcc ttccggtggg cgcggggcat gactatcgtc gccgcactta
         4261 tgactgtctt ctttatcatg caactcgtag gacaggtgcc ggcagcgctc ttccgcttcc
         4321 tcgctcactg actcgctgcg ctcggtcgtt cggctgcggc gagcggtatc agctcactca
         4381 aaggcggtaa tacggttatc cacagaatca ggggataacg caggaaagaa catgtgagca
         4441 aaaggccagc aaaaggccag gaaccgtaaa aaggccgcgt tgctggcgtt tttccatagg
         4501 ctccgccccc ctgacgagca tcacaaaaat cgacgctcaa gtcagaggtg gcgaaacccg
         4561 acaggactat aaagatacca ggcgtttccc cctggaagct ccctcgtgcg ctctcctgtt
         4621 ccgaccctgc cgcttaccgg atacctgtcc gcctttctcc cttcgggaag cgtggcgctt
         4681 tctcatagct cacgctgtag gtatctcagt tcggtgtagg tcgttcgctc caagctgggc
         4741 tgtgtgcacg aaccccccgt tcagcccgac cgctgcgcct tatccggtaa ctatcgtctt
         4801 gagtccaacc cggtaagaca cgacttatcg ccactggcag cagccactgg taacaggatt
         4861 agcagagcga ggtatgtagg cggtgctaca gagttcttga agtggtggcc taactacggc
         4921 tacactagaa gaacagtatt tggtatctgc gctctgctga agccagttac cttcggaaaa
         4981 agagttggta gctcttgatc cggcaaacaa accaccgctg gtagcggtgg tttttttgtt
         5041 tgcaagcagc agattacgcg cagaaaaaaa ggatctcaag aagatccttt gatcttttct
         5101 acggggtctg acgctcagtg gaacgaaaac tcacgttaag ggattttggt catgagatta
         5161 tcaaaaagga tcttcaccta gatcctttta aattaaaaat gaagttttaa atcaatctaa
         5221 agtatatatg agtaaacttg gtctgacagc ggccgcaaat gctaaaccac tgcagtggtt
         5281 accagtgctt gatcagtgag gcaccgatct cagcgatctg cctatttcgt tcgtccatag
         5341 tggcctgact ccccgtcgtg tagatcacta cgattcgtga gggcttacca tcaggcccca
         5401 gcgcagcaat gatgccgcga gagccgcgtt caccggcccc cgatttgtca gcaatgaacc
         5461 agccagcagg gagggccgag cgaagaagtg gtcctgctac tttgtccgcc tccatccagt
         5521 ctatgagctg ctgtcgtgat gctagagtaa gaagttcgcc agtgagtagt ttccgaagag
         5581 ttgtggccat tgctactggc atcgtggtat cacgctcgtc gttcggtatg gcttcgttca
         5641 actctggttc ccagcggtca agccgggtca catgatcacc catattatga agaaatgcag
         5701 tcagctcctt agggcctccg atcgttgtca gaagtaagtt ggccgcggtg ttgtcgctca
         5761 tggtaatggc agcactacac aattctctta ccgtcatgcc atccgtaaga tgcttttccg
         5821 tgaccggcga gtactcaacc aagtcgtttt gtgagtagtg tatacggcga ccaagctgct
         5881 cttgcccggc gtctatacgg gacaacaccg cgccacatag cagtactttg aaagtgctca
         5941 tcatcgggaa tcgttcttcg gggcggaaag actcaaggat cttgccgcta ttgagatcca
         6001 gttcgatata gcccactctt gcacccagtt gatcttcagc atcttttact ttcaccagcg
         6061 tttcggggtg tgcaaaaaca ggcaagcaaa atgccgcaaa gaagggaatg agtgcgacac
         6121 gaaaatgttg gatgctcat
    //

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