pGL4.41[luc2P/HSE/Hygro]载体

pGL4.41[luc2P/HSE/Hygro]载体

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  • ZYbscience
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  • ZY3751
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    • 详细信息
    • 询价记录
    • 技术资料
    • 保存条件

      -20℃低温保存

    • 保质期

      三年

    • 英文名

      pGL4.41[luc2P/HSE/Hygro]

    • 库存

      20

    • 供应商

      泽叶生物

    pGL4.41载体基本信息

    出品公司: ZYbscience
    载体名称: pGL4.41
    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: 6045 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: pGL4.41[luc2P/HSE/Hygro]载体是信号通路报告载体;含热激应答元件HSE;含萤火 虫荧光素酶报告基因luc2P。
    产品目录号: ZY3751
    稳定性: 稳表达
    组成型/诱导型: 组成型
    病毒/非病毒: 非病毒

    pGL4.41载体质粒图谱和多克隆位点信息

    pGL4.41载体图谱



    pGL4.41 载体特征

    pGL4.41载体简介

    The pGL4.41[luc2P/HSE/Hygro] Vector contains four copies of a heat shock response element (HSE) 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 pGL4.41[luc2P/HSE/Hygro] Vector is used to measure activation of the HSE in HepG2 cells upon treatment with 17-AAG or CdCl2. 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)
     17-AAG (17-(Allylamino)-17-demethoxygeldanamycin; Calbiochem Cat.# 100068)
     CdCl2 (Sigma Cat.# 202908)
     DMSO (Sigma Cat.# D2650)
     Dual-Glo Luciferase Assay System (Cat.# E2940)
     HepG2 cells
     pGL4.75[hRluc/CMV] Vector (Cat.# E6931)
    
    实验流程
    
    Day 1: Plate Cells
    1. Grow HepG2 cells in complete medium (DMEM + 10% FBS + 1X NEAA). Wash
    twice with DPBS and treat with one volume of 0.05% trypsin-EDTA, followed by four
    volumes of complete medium.
    2. Vigorously resuspend the cells by pipetting and allow cell clumps to settle. Remove
    the cell suspension from any cell clumps, quantify the cells and dilute in complete
    medium to 1 × 105 cells/ml.
    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 pGL4.41[luc2P/HSE/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 4.5:1 lipid:DNA ratio. Mix by pipetting. Incubate at room
    temperature for 20 minutes.
    3. Add 10μl 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. Resuspend 17-AAG (17-(Allylamino)-17-demethoxygeldanamycin) to 1mM in
    DMSO. Serially dilute into DMSO to give concentrated stock solutions (1,000X).
    Serially dilute a 1mM aqueous stock of CdCl2 into water to give concentrated stock
    solutions (1,000X). Dilute the 1,000X stocks of 17-AAG and CdCl2 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 17-AAG or CdCl2 and incubate for 6 hours in a 37°C,
    5% CO2 incubator.
    
    Day 4: Luminescence 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).
    
    

    pGL4.41载体序列

    LOCUS       JQ858520                6045 bp    DNA     circular SYN 02-JUL-2012
    DEFINITION  Reporter vector pGL4.41[luc2P/HSE/Hygro], complete sequence.
    ACCESSION   JQ858520
    VERSION     JQ858520.1  GI:392934110
    KEYWORDS    .
    SOURCE      Reporter vector pGL4.41[luc2P/HSE/Hygro]
      ORGANISM  Reporter vector pGL4.41[luc2P/HSE/Hygro]
                other sequences; artificial sequences; vectors.
    REFERENCE   1  (bases 1 to 6045)
      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..6045
                         /organism="Reporter vector pGL4.41[luc2P/HSE/Hygro]"
                         /mol_type="other DNA"
                         /db_xref="taxon:1203014"
         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..325
                         /regulatory_class="enhancer"
                         /note="HSE response element"
         regulatory      371..401
                         /regulatory_class="promoter"
                         /note="minP promoter"
         gene            434..2209
                         /gene="luc2P"
                         /note="synthetic luciferase"
         CDS             434..2209
                         /gene="luc2P"
                         /note="synthetic luciferase"
                         /codon_start=1
                         /transl_table=11
                         /product="luciferase"
                         /protein_id="AFM92248.1"
                         /db_xref="GI:392934112"
                         /translation="MEDAKNIKKGPAPFYPLEDGTAGEQLHKAMKRYALVPGTIAFTD
                         AHIEVDITYAEYFEMSVRLAEAMKRYGLNTNHRIVVCSENSLQFFMPVLGALFIGVAV
                         APANDIYNERELLNSMGISQPTVVFVSKKGLQKILNVQKKLPIIQKIIIMDSKTDYQG
                         FQSMYTFVTSHLPPGFNEYDFVPESFDRDKTIALIMNSSGSTGLPKGVALPHRTACVR
                         FSHARDPIFGNQIIPDTAILSVVPFHHGFGMFTTLGYLICGFRVVLMYRFEEELFLRS
                         LQDYKIQSALLVPTLFSFFAKSTLIDKYDLSNLHEIASGGAPLSKEVGEAVAKRFHLP
                         GIRQGYGLTETTSAILITPEGDDKPGAVGKVVPFFEAKVVDLDTGKTLGVNQRGELCV
                         RGPMIMSGYVNNPEATNALIDKDGWLHSGDIAYWDEDEHFFIVDRLKSLIKYKGYQVA
                         PAELESILLQHPNIFDAGVAGLPDDDAGELPAAVVVLEHGKTMTEKEIVDYVASQVTT
                         AKKLRGGVVFVDEVPKGLTGKLDARKIREILIKAKKGGKIAVNSHGFPPEVEEQAAGT
                         LPMSCAQESGMDRHPAACASARINV"
         regulatory      2249..2470
                         /regulatory_class="polyA_signal_sequence"
                         /note="SV40 late poly(A) signal"
         regulatory      2518..2936
                         /regulatory_class="enhancer"
                         /note="SV40 enhancer and early promoter"
         CDS             2961..3998
                         /note="hygromycin resistance"
                         /codon_start=1
                         /transl_table=11
                         /product="hygromycin phosphotransferase"
                         /protein_id="AFM92249.1"
                         /db_xref="GI:392934113"
                         /translation="MKKPELTATSVEKFLIEKFDSVSDLMQLSEGEESRAFSFDVGGR
                         GYVLRVNSCADGFYKDRYVYRHFASAALPIPEVLDIGEFSESLTYCISRRAQGVTLQD
                         LPETELPAVLQPVAEAMDAIAAADLSQTSGFGPFGPQGIGQYTTWRDFICAIADPHVY
                         HWQTVMDDTVSASVAQALDELMLWAEDCPEVRHLVHADFGSNNVLTDNGRITAVIDWS
                         EAMFGDSQYEVANIFFWRPWLACMEQQTRYFERRHPELAGSPRLRAYMLRIGLDQLYQ
                         SLVDGNFDDAAWAQGRCDAIVRSGAGTVGRTQIARRSAAVWTDGCVEVLADSGNRRPS
                         TRPRAKEVGRV"
         regulatory      4022..4070
                         /regulatory_class="polyA_signal_sequence"
                         /note="synthetic poly(A) signal sequence"
         primer_bind     complement(4137..4156)
                         /note="RVprimer4 binding site"
         rep_origin      4394..4430
         gene            complement(5185..6045)
                         /gene="bla"
                         /note="AmpR"
         CDS             complement(5185..6045)
                         /gene="bla"
                         /note="AmpR"
                         /codon_start=1
                         /transl_table=11
                         /product="beta-lactamase"
                         /protein_id="AFM92247.1"
                         /db_xref="GI:392934111"
                         /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 gctcctggaa gattctagaa
          301 cgttctggaa gattctagaa cgttcctcga ggatatcaag atctggcctc ggcggccaag
          361 cttagacact agagggtata taatggaagc tcgacttcca gcttggcaat ccggtactgt
          421 tggtaaagcc accatggaag atgccaaaaa cattaagaag ggcccagcgc cattctaccc
          481 actcgaagac gggaccgccg gcgagcagct gcacaaagcc atgaagcgct acgccctggt
          541 gcccggcacc atcgccttta ccgacgcaca tatcgaggtg gacattacct acgccgagta
          601 cttcgagatg agcgttcggc tggcagaagc tatgaagcgc tatgggctga atacaaacca
          661 tcggatcgtg gtgtgcagcg agaatagctt gcagttcttc atgcccgtgt tgggtgccct
          721 gttcatcggt gtggctgtgg ccccagctaa cgacatctac aacgagcgcg agctgctgaa
          781 cagcatgggc atcagccagc ccaccgtcgt attcgtgagc aagaaagggc tgcaaaagat
          841 cctcaacgtg caaaagaagc taccgatcat acaaaagatc atcatcatgg atagcaagac
          901 cgactaccag ggcttccaaa gcatgtacac cttcgtgact tcccatttgc cacccggctt
          961 caacgagtac gacttcgtgc ccgagagctt cgaccgggac aaaaccatcg ccctgatcat
         1021 gaacagtagt ggcagtaccg gattgcccaa gggcgtagcc ctaccgcacc gcaccgcttg
         1081 tgtccgattc agtcatgccc gcgaccccat cttcggcaac cagatcatcc ccgacaccgc
         1141 tatcctcagc gtggtgccat ttcaccacgg cttcggcatg ttcaccacgc tgggctactt
         1201 gatctgcggc tttcgggtcg tgctcatgta ccgcttcgag gaggagctat tcttgcgcag
         1261 cttgcaagac tataagattc aatctgccct gctggtgccc acactattta gcttcttcgc
         1321 taagagcact ctcatcgaca agtacgacct aagcaacttg cacgagatcg ccagcggcgg
         1381 ggcgccgctc agcaaggagg taggtgaggc cgtggccaaa cgcttccacc taccaggcat
         1441 ccgccagggc tacggcctga cagaaacaac cagcgccatt ctgatcaccc ccgaagggga
         1501 cgacaagcct ggcgcagtag gcaaggtggt gcccttcttc gaggctaagg tggtggactt
         1561 ggacaccggt aagacactgg gtgtgaacca gcgcggcgag ctgtgcgtcc gtggccccat
         1621 gatcatgagc ggctacgtta acaaccccga ggctacaaac gctctcatcg acaaggacgg
         1681 ctggctgcac agcggcgaca tcgcctactg ggacgaggac gagcacttct tcatcgtgga
         1741 ccggctgaag agcctgatca aatacaaggg ctaccaggta gccccagccg aactggagag
         1801 catcctgctg caacacccca acatcttcga cgccggggtc gccggcctgc ccgacgacga
         1861 tgccggcgag ctgcccgccg cagtcgtcgt gctggaacac ggtaaaacca tgaccgagaa
         1921 ggagatcgtg gactatgtgg ccagccaggt tacaaccgcc aagaagctgc gcggtggtgt
         1981 tgtgttcgtg gacgaggtgc ctaaaggact gaccggcaag ttggacgccc gcaagatccg
         2041 cgagattctc attaaggcca agaagggcgg caagatcgcc gtgaattctc acggcttccc
         2101 tcccgaggtg gaggagcagg ccgccggcac cctgcccatg agctgcgccc aggagagcgg
         2161 catggataga caccctgctg cttgcgccag cgccaggatc aacgtctaag gccgcgactc
         2221 tagagtcggg gcggccggcc gcttcgagca gacatgataa gatacattga tgagtttgga
         2281 caaaccacaa ctagaatgca gtgaaaaaaa tgctttattt gtgaaatttg tgatgctatt
         2341 gctttatttg taaccattat aagctgcaat aaacaagtta acaacaacaa ttgcattcat
         2401 tttatgtttc aggttcaggg ggaggtgtgg gaggtttttt aaagcaagta aaacctctac
         2461 aaatgtggta aaatcgataa ggatccgttt gcgtattggg cgctcttccg ctgatctgcg
         2521 cagcaccatg gcctgaaata acctctgaaa gaggaacttg gttagctacc ttctgaggcg
         2581 gaaagaacca gctgtggaat gtgtgtcagt tagggtgtgg aaagtcccca ggctccccag
         2641 caggcagaag tatgcaaagc atgcatctca attagtcagc aaccaggtgt ggaaagtccc
         2701 caggctcccc agcaggcaga agtatgcaaa gcatgcatct caattagtca gcaaccatag
         2761 tcccgcccct aactccgccc atcccgcccc taactccgcc cagttccgcc cattctccgc
         2821 cccatggctg actaattttt tttatttatg cagaggccga ggccgcctct gcctctgagc
         2881 tattccagaa gtagtgagga ggcttttttg gaggcctagg cttttgcaaa aagctcgatt
         2941 cttctgacac tagcgccacc atgaagaagc ccgaactcac cgctaccagc gttgaaaaat
         3001 ttctcatcga gaagttcgac agtgtgagcg acctgatgca gttgtcggag ggcgaagaga
         3061 gccgagcctt cagcttcgat gtcggcggac gcggctatgt actgcgggtg aatagctgcg
         3121 ctgatggctt ctacaaagac cgctacgtgt accgccactt cgccagcgct gcactaccca
         3181 tccccgaagt gttggacatc ggcgagttca gcgagagcct gacatactgc atcagtagac
         3241 gcgcccaagg cgttactctc caagacctcc ccgaaacaga gctgcctgct gtgttacagc
         3301 ctgtcgccga agctatggat gctattgccg ccgccgacct cagtcaaacc agcggcttcg
         3361 gcccattcgg gccccaaggc atcggccagt acacaacctg gcgggatttc atttgcgcca
         3421 ttgctgatcc ccatgtctac cactggcaga ccgtgatgga cgacaccgtg tccgccagcg
         3481 tagctcaagc cctggacgaa ctgatgctgt gggccgaaga ctgtcccgag gtgcgccacc
         3541 tcgtccatgc cgacttcggc agcaacaacg tcctgaccga caacggccgc atcaccgccg
         3601 taatcgactg gtccgaagct atgttcgggg acagtcagta cgaggtggcc aacatcttct
         3661 tctggcggcc ctggctggct tgcatggagc agcagactcg ctacttcgag cgccggcatc
         3721 ccgagctggc cggcagccct cgtctgcgag cctacatgct gcgcatcggc ctggatcagc
         3781 tctaccagag cctcgtggac ggcaacttcg acgatgctgc ctgggctcaa ggccgctgcg
         3841 atgccatcgt ccgcagcggg gccggcaccg tcggtcgcac acaaatcgct cgccggagcg
         3901 cagccgtatg gaccgacggc tgcgtcgagg tgctggccga cagcggcaac cgccggccca
         3961 gtacacgacc gcgcgctaag gaggtaggtc gagtttaaac tctagaaccg gtcatggccg
         4021 caataaaata tctttatttt cattacatct gtgtgttggt tttttgtgtg ttcgaactag
         4081 atgctgtcga ccgatgccct tgagagcctt caacccagtc agctccttcc ggtgggcgcg
         4141 gggcatgact atcgtcgccg cacttatgac tgtcttcttt atcatgcaac tcgtaggaca
         4201 ggtgccggca gcgctcttcc gcttcctcgc tcactgactc gctgcgctcg gtcgttcggc
         4261 tgcggcgagc ggtatcagct cactcaaagg cggtaatacg gttatccaca gaatcagggg
         4321 ataacgcagg aaagaacatg tgagcaaaag gccagcaaaa ggccaggaac cgtaaaaagg
         4381 ccgcgttgct ggcgtttttc cataggctcc gcccccctga cgagcatcac aaaaatcgac
         4441 gctcaagtca gaggtggcga aacccgacag gactataaag ataccaggcg tttccccctg
         4501 gaagctccct cgtgcgctct cctgttccga ccctgccgct taccggatac ctgtccgcct
         4561 ttctcccttc gggaagcgtg gcgctttctc atagctcacg ctgtaggtat ctcagttcgg
         4621 tgtaggtcgt tcgctccaag ctgggctgtg tgcacgaacc ccccgttcag cccgaccgct
         4681 gcgccttatc cggtaactat cgtcttgagt ccaacccggt aagacacgac ttatcgccac
         4741 tggcagcagc cactggtaac aggattagca gagcgaggta tgtaggcggt gctacagagt
         4801 tcttgaagtg gtggcctaac tacggctaca ctagaagaac agtatttggt atctgcgctc
         4861 tgctgaagcc agttaccttc ggaaaaagag ttggtagctc ttgatccggc aaacaaacca
         4921 ccgctggtag cggtggtttt tttgtttgca agcagcagat tacgcgcaga aaaaaaggat
         4981 ctcaagaaga tcctttgatc ttttctacgg ggtctgacgc tcagtggaac gaaaactcac
         5041 gttaagggat tttggtcatg agattatcaa aaaggatctt cacctagatc cttttaaatt
         5101 aaaaatgaag ttttaaatca atctaaagta tatatgagta aacttggtct gacagcggcc
         5161 gcaaatgcta aaccactgca gtggttacca gtgcttgatc agtgaggcac cgatctcagc
         5221 gatctgccta tttcgttcgt ccatagtggc ctgactcccc gtcgtgtaga tcactacgat
         5281 tcgtgagggc ttaccatcag gccccagcgc agcaatgatg ccgcgagagc cgcgttcacc
         5341 ggcccccgat ttgtcagcaa tgaaccagcc agcagggagg gccgagcgaa gaagtggtcc
         5401 tgctactttg tccgcctcca tccagtctat gagctgctgt cgtgatgcta gagtaagaag
         5461 ttcgccagtg agtagtttcc gaagagttgt ggccattgct actggcatcg tggtatcacg
         5521 ctcgtcgttc ggtatggctt cgttcaactc tggttcccag cggtcaagcc gggtcacatg
         5581 atcacccata ttatgaagaa atgcagtcag ctccttaggg cctccgatcg ttgtcagaag
         5641 taagttggcc gcggtgttgt cgctcatggt aatggcagca ctacacaatt ctcttaccgt
         5701 catgccatcc gtaagatgct tttccgtgac cggcgagtac tcaaccaagt cgttttgtga
         5761 gtagtgtata cggcgaccaa gctgctcttg cccggcgtct atacgggaca acaccgcgcc
         5821 acatagcagt actttgaaag tgctcatcat cgggaatcgt tcttcggggc ggaaagactc
         5881 aaggatcttg ccgctattga gatccagttc gatatagccc actcttgcac ccagttgatc
         5941 ttcagcatct tttactttca ccagcgtttc ggggtgtgca aaaacaggca agcaaaatgc
         6001 cgcaaagaag ggaatgagtg cgacacgaaa atgttggatg ctcat
    //

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