pGL4.37[luc2P/ARE/Hygro]载体

pGL4.37[luc2P/ARE/Hygro]载体

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  • ZYbscience
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  • ZY3641
  • 2025年07月12日
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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

      pGL4.37[luc2P/ARE/Hygro]

    • 库存

      20

    • 供应商

      泽叶生物

    pGL4.37载体基本信息

    出品公司: ZYbscience
    载体名称: pGL4.37 ; pGL4.37[luc2P/ARE/Hygro]
    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:
    载体大小: 6086 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
    备注:
    pGL4.37[luc2P]载体是信号通路报告载体;含ARE应答元件;含萤火虫荧光素酶报告基因luc2P。
    产品目录号: ZY3641
    稳定性: 稳表达
    组成型/诱导型: 组成型
    病毒/非病毒: 非病毒

    pGL4.37载体质粒图谱和多克隆位点信息

    pGL4.37载体图谱



    pGL4.37 载体特征

    pGL4.37载体简介

    The pGL4.37[luc2P/ARE/Hygro] Vector contains four copies of an antioxidant response element (ARE) 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.
    
    
    In this example protocol, the pGL4.37[luc2P/ARE/Hygro] Vector is used to measure activation of the ARE in HEK293 cells upon treatment with tert-Butylhydroquinone or D,LSulforaphane.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
     Dulbecco’s PBS (DPBS; Life Technologies Cat.# 14190)
     0.05% Tryspin-EDTA (Life Technologies Cat.# 25300)
     DMEM (Life Technologies Cat.# 11995)
     complete medium (DMEM supplemented with 10% fetal bovine serum
    [Life Technologies Cat.# 11995] and 1X NEAA [Life Technologies Cat.# 11140])
     Charcoal-stripped FBS (Life Technologies Cat.# 126776-011)
     DMSO (Sigma Cat.# D2650)
     Opti-MEM I (Life Technologies Cat.# 31985)
     FuGENE HD Transfection Reagent (Cat.# E2311)
     tert-Butylhydroquinone (Sigma Cat.# 112941)
    or D,L-Sulforaphane (Sigma Cat.# S4441)
     Dual-Glo Luciferase Assay System (Cat.# E2940)
     HEK293 cells
     pGL4.75[hRluc/CMV] Vector (Cat.# E6931)
    
    
    实验流程
    
    Day 1: Plate Cells
    
    1. Grow HEK293 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. Quantify the cells and dilute to 1.5 × 105 cells/ml in complete medium.
    3. Plate 100μl per well to a solid, white 96-well plate (Corning Cat.# 3917).
    4. Incubate for 24 hours in a 37°C, 5% CO2 incubator.
    
    Day 2: Transfection
    
    1. Dilute pGL4.37[luc2P/ARE/Hygro] and pGL4.75 [hRluc/CMV] Renilla luciferase vector
    constructs in a 10:1 mass ratio, respectively, to 12.5ng 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 20 minutes.
    3. Add 8μl transfection complex per well (100ng DNA/well) and incubate for 18 hours
    in a 37°C, 5% CO2 incubator.
    
    Day 3: Medium Replacement and Cell Treatment
    
    1. Remove medium from cells and replace with 72μl of DMEM + 0.5% charcoalstripped
    FBS per well.
    2. Incubate for 6 hours in a 37°C, 5% CO2 incubator.
    3. Resuspend tert-Butylhydroquinone (tBHQ) to 500mM in ethanol. Serially dilute into
    ethanol to give 1,000X stocks. Resuspend D,L-Sulforaphane to 200mM in DMSO.
    Serially dilute into DMSO to give 1,000X stocks. Dilute the 1,000X stocks into Opti-
    MEM I to give 10X stocks.
    4. Add 8 μl of the 10X stocks of tBHQ or D,L-Sulforaphane to each well and incubate
    for 18 hours in a 37°C, 5% CO2 incubator.
    
    Day 4: Luciferase Measurement
    
    1. Remove plates from the 37°C, 5% CO2 incubator and allow to cool to room temperature
    for approximately 15 minutes.
    2. 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).
    
    

    pGL4.37载体序列

    LOCUS       JQ858521                6086 bp    DNA     circular SYN 02-JUL-2012
    DEFINITION  Reporter vector pGL4.37[luc2P/ARE/Hygro], complete sequence.
    ACCESSION   JQ858521
    VERSION     JQ858521.1  GI:392934114
    KEYWORDS    .
    SOURCE      Reporter vector pGL4.37[luc2P/ARE/Hygro]
      ORGANISM  Reporter vector pGL4.37[luc2P/ARE/Hygro]
                other sequences; artificial sequences; vectors.
    REFERENCE   1  (bases 1 to 6086)
      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..6086
                         /organism="Reporter vector pGL4.37[luc2P/ARE/Hygro]"
                         /mol_type="other DNA"
                         /db_xref="taxon:1203015"
         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..366
                         /regulatory_class="enhancer"
                         /note="antioxidant response element (ARE)"
         regulatory      412..442
                         /regulatory_class="promoter"
                         /note="minP promoter"
         gene            475..2250
                         /gene="luc2P"
                         /note="synthetic luciferase"
         CDS             475..2250
                         /gene="luc2P"
                         /note="synthetic luciferase"
                         /codon_start=1
                         /transl_table=11
                         /product="luciferase"
                         /protein_id="AFM92251.1"
                         /db_xref="GI:392934116"
                         /translation="MEDAKNIKKGPAPFYPLEDGTAGEQLHKAMKRYALVPGTIAFTD
                         AHIEVDITYAEYFEMSVRLAEAMKRYGLNTNHRIVVCSENSLQFFMPVLGALFIGVAV
                         APANDIYNERELLNSMGISQPTVVFVSKKGLQKILNVQKKLPIIQKIIIMDSKTDYQG
                         FQSMYTFVTSHLPPGFNEYDFVPESFDRDKTIALIMNSSGSTGLPKGVALPHRTACVR
                         FSHARDPIFGNQIIPDTAILSVVPFHHGFGMFTTLGYLICGFRVVLMYRFEEELFLRS
                         LQDYKIQSALLVPTLFSFFAKSTLIDKYDLSNLHEIASGGAPLSKEVGEAVAKRFHLP
                         GIRQGYGLTETTSAILITPEGDDKPGAVGKVVPFFEAKVVDLDTGKTLGVNQRGELCV
                         RGPMIMSGYVNNPEATNALIDKDGWLHSGDIAYWDEDEHFFIVDRLKSLIKYKGYQVA
                         PAELESILLQHPNIFDAGVAGLPDDDAGELPAAVVVLEHGKTMTEKEIVDYVASQVTT
                         AKKLRGGVVFVDEVPKGLTGKLDARKIREILIKAKKGGKIAVNSHGFPPEVEEQAAGT
                         LPMSCAQESGMDRHPAACASARINV"
         regulatory      2290..2511
                         /regulatory_class="polyA_signal_sequence"
                         /note="SV40 late poly(A) signal"
         regulatory      2559..2977
                         /regulatory_class="enhancer"
                         /note="SV40 enhancer and early promoter"
         CDS             3002..4039
                         /note="hygromycin resistance"
                         /codon_start=1
                         /transl_table=11
                         /product="hygromycin phosphotransferase"
                         /protein_id="AFM92252.1"
                         /db_xref="GI:392934117"
                         /translation="MKKPELTATSVEKFLIEKFDSVSDLMQLSEGEESRAFSFDVGGR
                         GYVLRVNSCADGFYKDRYVYRHFASAALPIPEVLDIGEFSESLTYCISRRAQGVTLQD
                         LPETELPAVLQPVAEAMDAIAAADLSQTSGFGPFGPQGIGQYTTWRDFICAIADPHVY
                         HWQTVMDDTVSASVAQALDELMLWAEDCPEVRHLVHADFGSNNVLTDNGRITAVIDWS
                         EAMFGDSQYEVANIFFWRPWLACMEQQTRYFERRHPELAGSPRLRAYMLRIGLDQLYQ
                         SLVDGNFDDAAWAQGRCDAIVRSGAGTVGRTQIARRSAAVWTDGCVEVLADSGNRRPS
                         TRPRAKEVGRV"
         regulatory      4063..4111
                         /regulatory_class="polyA_signal_sequence"
                         /note="synthetic poly(A) signal sequence"
         primer_bind     complement(4178..4197)
                         /note="RVprimer4 binding site"
         rep_origin      4435..4471
         gene            complement(5226..6086)
                         /gene="bla"
                         /note="AmpR"
         CDS             complement(5226..6086)
                         /gene="bla"
                         /note="AmpR"
                         /codon_start=1
                         /transl_table=11
                         /product="beta-lactamase"
                         /protein_id="AFM92250.1"
                         /db_xref="GI:392934115"
                         /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 gctctagctt ggaaatgaca
          301 ttgctaatgg tgacaaagca acttttagct tggaaatgac attgctaatg gtgacaaagc
          361 aactttctcg aggatatcaa gatctggcct cggcggccaa gcttagacac tagagggtat
          421 ataatggaag ctcgacttcc agcttggcaa tccggtactg ttggtaaagc caccatggaa
          481 gatgccaaaa acattaagaa gggcccagcg ccattctacc cactcgaaga cgggaccgcc
          541 ggcgagcagc tgcacaaagc catgaagcgc tacgccctgg tgcccggcac catcgccttt
          601 accgacgcac atatcgaggt ggacattacc tacgccgagt acttcgagat gagcgttcgg
          661 ctggcagaag ctatgaagcg ctatgggctg aatacaaacc atcggatcgt ggtgtgcagc
          721 gagaatagct tgcagttctt catgcccgtg ttgggtgccc tgttcatcgg tgtggctgtg
          781 gccccagcta acgacatcta caacgagcgc gagctgctga acagcatggg catcagccag
          841 cccaccgtcg tattcgtgag caagaaaggg ctgcaaaaga tcctcaacgt gcaaaagaag
          901 ctaccgatca tacaaaagat catcatcatg gatagcaaga ccgactacca gggcttccaa
          961 agcatgtaca ccttcgtgac ttcccatttg ccacccggct tcaacgagta cgacttcgtg
         1021 cccgagagct tcgaccggga caaaaccatc gccctgatca tgaacagtag tggcagtacc
         1081 ggattgccca agggcgtagc cctaccgcac cgcaccgctt gtgtccgatt cagtcatgcc
         1141 cgcgacccca tcttcggcaa ccagatcatc cccgacaccg ctatcctcag cgtggtgcca
         1201 tttcaccacg gcttcggcat gttcaccacg ctgggctact tgatctgcgg ctttcgggtc
         1261 gtgctcatgt accgcttcga ggaggagcta ttcttgcgca gcttgcaaga ctataagatt
         1321 caatctgccc tgctggtgcc cacactattt agcttcttcg ctaagagcac tctcatcgac
         1381 aagtacgacc taagcaactt gcacgagatc gccagcggcg gggcgccgct cagcaaggag
         1441 gtaggtgagg ccgtggccaa acgcttccac ctaccaggca tccgccaggg ctacggcctg
         1501 acagaaacaa ccagcgccat tctgatcacc cccgaagggg acgacaagcc tggcgcagta
         1561 ggcaaggtgg tgcccttctt cgaggctaag gtggtggact tggacaccgg taagacactg
         1621 ggtgtgaacc agcgcggcga gctgtgcgtc cgtggcccca tgatcatgag cggctacgtt
         1681 aacaaccccg aggctacaaa cgctctcatc gacaaggacg gctggctgca cagcggcgac
         1741 atcgcctact gggacgagga cgagcacttc ttcatcgtgg accggctgaa gagcctgatc
         1801 aaatacaagg gctaccaggt agccccagcc gaactggaga gcatcctgct gcaacacccc
         1861 aacatcttcg acgccggggt cgccggcctg cccgacgacg atgccggcga gctgcccgcc
         1921 gcagtcgtcg tgctggaaca cggtaaaacc atgaccgaga aggagatcgt ggactatgtg
         1981 gccagccagg ttacaaccgc caagaagctg cgcggtggtg ttgtgttcgt ggacgaggtg
         2041 cctaaaggac tgaccggcaa gttggacgcc cgcaagatcc gcgagattct cattaaggcc
         2101 aagaagggcg gcaagatcgc cgtgaattct cacggcttcc ctcccgaggt ggaggagcag
         2161 gccgccggca ccctgcccat gagctgcgcc caggagagcg gcatggatag acaccctgct
         2221 gcttgcgcca gcgccaggat caacgtctaa ggccgcgact ctagagtcgg ggcggccggc
         2281 cgcttcgagc agacatgata agatacattg atgagtttgg acaaaccaca actagaatgc
         2341 agtgaaaaaa atgctttatt tgtgaaattt gtgatgctat tgctttattt gtaaccatta
         2401 taagctgcaa taaacaagtt aacaacaaca attgcattca ttttatgttt caggttcagg
         2461 gggaggtgtg ggaggttttt taaagcaagt aaaacctcta caaatgtggt aaaatcgata
         2521 aggatccgtt tgcgtattgg gcgctcttcc gctgatctgc gcagcaccat ggcctgaaat
         2581 aacctctgaa agaggaactt ggttagctac cttctgaggc ggaaagaacc agctgtggaa
         2641 tgtgtgtcag ttagggtgtg gaaagtcccc aggctcccca gcaggcagaa gtatgcaaag
         2701 catgcatctc aattagtcag caaccaggtg tggaaagtcc ccaggctccc cagcaggcag
         2761 aagtatgcaa agcatgcatc tcaattagtc agcaaccata gtcccgcccc taactccgcc
         2821 catcccgccc ctaactccgc ccagttccgc ccattctccg ccccatggct gactaatttt
         2881 ttttatttat gcagaggccg aggccgcctc tgcctctgag ctattccaga agtagtgagg
         2941 aggctttttt ggaggcctag gcttttgcaa aaagctcgat tcttctgaca ctagcgccac
         3001 catgaagaag cccgaactca ccgctaccag cgttgaaaaa tttctcatcg agaagttcga
         3061 cagtgtgagc gacctgatgc agttgtcgga gggcgaagag agccgagcct tcagcttcga
         3121 tgtcggcgga cgcggctatg tactgcgggt gaatagctgc gctgatggct tctacaaaga
         3181 ccgctacgtg taccgccact tcgccagcgc tgcactaccc atccccgaag tgttggacat
         3241 cggcgagttc agcgagagcc tgacatactg catcagtaga cgcgcccaag gcgttactct
         3301 ccaagacctc cccgaaacag agctgcctgc tgtgttacag cctgtcgccg aagctatgga
         3361 tgctattgcc gccgccgacc tcagtcaaac cagcggcttc ggcccattcg ggccccaagg
         3421 catcggccag tacacaacct ggcgggattt catttgcgcc attgctgatc cccatgtcta
         3481 ccactggcag accgtgatgg acgacaccgt gtccgccagc gtagctcaag ccctggacga
         3541 actgatgctg tgggccgaag actgtcccga ggtgcgccac ctcgtccatg ccgacttcgg
         3601 cagcaacaac gtcctgaccg acaacggccg catcaccgcc gtaatcgact ggtccgaagc
         3661 tatgttcggg gacagtcagt acgaggtggc caacatcttc ttctggcggc cctggctggc
         3721 ttgcatggag cagcagactc gctacttcga gcgccggcat cccgagctgg ccggcagccc
         3781 tcgtctgcga gcctacatgc tgcgcatcgg cctggatcag ctctaccaga gcctcgtgga
         3841 cggcaacttc gacgatgctg cctgggctca aggccgctgc gatgccatcg tccgcagcgg
         3901 ggccggcacc gtcggtcgca cacaaatcgc tcgccggagc gcagccgtat ggaccgacgg
         3961 ctgcgtcgag gtgctggccg acagcggcaa ccgccggccc agtacacgac cgcgcgctaa
         4021 ggaggtaggt cgagtttaaa ctctagaacc ggtcatggcc gcaataaaat atctttattt
         4081 tcattacatc tgtgtgttgg ttttttgtgt gttcgaacta gatgctgtcg accgatgccc
         4141 ttgagagcct tcaacccagt cagctccttc cggtgggcgc ggggcatgac tatcgtcgcc
         4201 gcacttatga ctgtcttctt tatcatgcaa ctcgtaggac aggtgccggc agcgctcttc
         4261 cgcttcctcg ctcactgact cgctgcgctc ggtcgttcgg ctgcggcgag cggtatcagc
         4321 tcactcaaag gcggtaatac ggttatccac agaatcaggg gataacgcag gaaagaacat
         4381 gtgagcaaaa ggccagcaaa aggccaggaa ccgtaaaaag gccgcgttgc tggcgttttt
         4441 ccataggctc cgcccccctg acgagcatca caaaaatcga cgctcaagtc agaggtggcg
         4501 aaacccgaca ggactataaa gataccaggc gtttccccct ggaagctccc tcgtgcgctc
         4561 tcctgttccg accctgccgc ttaccggata cctgtccgcc tttctccctt cgggaagcgt
         4621 ggcgctttct catagctcac gctgtaggta tctcagttcg gtgtaggtcg ttcgctccaa
         4681 gctgggctgt gtgcacgaac cccccgttca gcccgaccgc tgcgccttat ccggtaacta
         4741 tcgtcttgag tccaacccgg taagacacga cttatcgcca ctggcagcag ccactggtaa
         4801 caggattagc agagcgaggt atgtaggcgg tgctacagag ttcttgaagt ggtggcctaa
         4861 ctacggctac actagaagaa cagtatttgg tatctgcgct ctgctgaagc cagttacctt
         4921 cggaaaaaga gttggtagct cttgatccgg caaacaaacc accgctggta gcggtggttt
         4981 ttttgtttgc aagcagcaga ttacgcgcag aaaaaaagga tctcaagaag atcctttgat
         5041 cttttctacg gggtctgacg ctcagtggaa cgaaaactca cgttaaggga ttttggtcat
         5101 gagattatca aaaaggatct tcacctagat ccttttaaat taaaaatgaa gttttaaatc
         5161 aatctaaagt atatatgagt aaacttggtc tgacagcggc cgcaaatgct aaaccactgc
         5221 agtggttacc agtgcttgat cagtgaggca ccgatctcag cgatctgcct atttcgttcg
         5281 tccatagtgg cctgactccc cgtcgtgtag atcactacga ttcgtgaggg cttaccatca
         5341 ggccccagcg cagcaatgat gccgcgagag ccgcgttcac cggcccccga tttgtcagca
         5401 atgaaccagc cagcagggag ggccgagcga agaagtggtc ctgctacttt gtccgcctcc
         5461 atccagtcta tgagctgctg tcgtgatgct agagtaagaa gttcgccagt gagtagtttc
         5521 cgaagagttg tggccattgc tactggcatc gtggtatcac gctcgtcgtt cggtatggct
         5581 tcgttcaact ctggttccca gcggtcaagc cgggtcacat gatcacccat attatgaaga
         5641 aatgcagtca gctccttagg gcctccgatc gttgtcagaa gtaagttggc cgcggtgttg
         5701 tcgctcatgg taatggcagc actacacaat tctcttaccg tcatgccatc cgtaagatgc
         5761 ttttccgtga ccggcgagta ctcaaccaag tcgttttgtg agtagtgtat acggcgacca
         5821 agctgctctt gcccggcgtc tatacgggac aacaccgcgc cacatagcag tactttgaaa
         5881 gtgctcatca tcgggaatcg ttcttcgggg cggaaagact caaggatctt gccgctattg
         5941 agatccagtt cgatatagcc cactcttgca cccagttgat cttcagcatc ttttactttc
         6001 accagcgttt cggggtgtgc aaaaacaggc aagcaaaatg ccgcaaagaa gggaatgagt
         6061 gcgacacgaa aatgttggat gctcat

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