pGL4.42[luc2P/HRE/Hygro]载体

pGL4.42[luc2P/HRE/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

      pGL4.42[luc2P/HRE/Hygro]

    • 库存

      20

    • 供应商

      泽叶生物

    pGL4.42载体基本信息

    出品公司: ZYbscience
    载体名称: pGL4.42 ; pGL4.42[luc2P/HRE/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: Minimal Promotor
    载体大小: 6080 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: pGL4.42[luc2P/HRE/Hygro]载体是信号通路报告载体;含氧缺乏应答元件HRE;含萤火 虫荧光素酶报告基因luc2P。
    产品目录号: ZY4001
    稳定性: 稳表达
    组成型/诱导型: 组成型
    病毒/非病毒: 非病毒

    pGL4.42载体质粒图谱和多克隆位点信息

    pGL4.42载体图谱



    pGL4.42 载体特征

    pGL4.42载体简介

    pGL4.42载体介绍
    The pGL4.42[luc2P/HRE/Hygro] Vector contains four copies of a hypoxia response element (HRE) 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 pGL4.42[luc2P/HRE/Hygro] Vector is used to measure
    activation of the HRE in HEK293 cells upon treatment with 1,10-phenanthroline. 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 (DMEM/FBS;
    Life Technologies Cat.# 16000) and 1X NEAA (Life Technologies Cat.# 11140)
     Opti-MEM I (Life Technologies Cat.# 31985)
     FuGENE HD Transfection Reagent (Cat.# E2311)
     DMSO (Sigma Cat.# D2650)
     1,10-phenanthroline (Sigma Cat.# 131377))
     Dual-Glo Luciferase Assay System (Cat.# E2940)
     HEK293 cells
     pGL4.75[hRluc/CMV] Vector (Cat.# E6931)
    
    实验流程
    Day 1: Reverse Transfection
    Preparation of 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. Pellet the cells by centrifugation at 233 x 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 pGL4.42[luc2P/HRE/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. Mix by
    pipetting.
    4. Plate 100μl per well into a solid, white 96-well plate (Corning Cat.# 3917).
    5. Incubate for 24 hours in a 37°C, 5% CO2 incubator.
    
    Day 2: Cell Treatment and Luminescence Measurement
    1. Dissolve 1,10-phenanthroline to a final concentration of 50mM in DMSO. Serially
    dilute this solution using DMSO to give a range of concentrated stock solutions
    (500X). Dilute each concentrated stock solution using Opti-MEM I to give a range
    of dilute stock solutions (10X). Add 10μl of the 10X stocks to each well.
    2. Incubate for 5 hours in a 37°C, 5% CO2 incubator.
    3. Remove plates from the 37°C, 5% CO2 incubator. Allow plates to cool to room
    temperature for approximately 15 minutes.
    4. Add 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).
    
    

    pGL4.42载体序列

    LOCUS       JQ858518                6080 bp    DNA     circular SYN 02-JUL-2012
    DEFINITION  Reporter vector PGL4.42 [luc2P/HRE/Hygro], complete sequence.
    ACCESSION   JQ858518
    VERSION     JQ858518.1  GI:392934102
    KEYWORDS    .
    SOURCE      Reporter vector PGL4.42 [luc2P/HRE/Hygro]
      ORGANISM  Reporter vector PGL4.42 [luc2P/HRE/Hygro]
                other sequences; artificial sequences; vectors.
    REFERENCE   1  (bases 1 to 6080)
      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..6080
                         /organism="Reporter vector PGL4.42 [luc2P/HRE/Hygro]"
                         /mol_type="other DNA"
                         /db_xref="taxon:1203012"
         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"
         misc_feature    285..360
                         /note="HRE response element"
         regulatory      406..436
                         /regulatory_class="promoter"
                         /note="minP promoter"
         gene            469..2244
                         /gene="luc2P"
                         /note="synthetic luciferase"
         CDS             469..2244
                         /gene="luc2P"
                         /note="synthetic luciferase"
                         /codon_start=1
                         /transl_table=11
                         /product="luciferase"
                         /protein_id="AFM92242.1"
                         /db_xref="GI:392934104"
                         /translation="MEDAKNIKKGPAPFYPLEDGTAGEQLHKAMKRYALVPGTIAFTD
                         AHIEVDITYAEYFEMSVRLAEAMKRYGLNTNHRIVVCSENSLQFFMPVLGALFIGVAV
                         APANDIYNERELLNSMGISQPTVVFVSKKGLQKILNVQKKLPIIQKIIIMDSKTDYQG
                         FQSMYTFVTSHLPPGFNEYDFVPESFDRDKTIALIMNSSGSTGLPKGVALPHRTACVR
                         FSHARDPIFGNQIIPDTAILSVVPFHHGFGMFTTLGYLICGFRVVLMYRFEEELFLRS
                         LQDYKIQSALLVPTLFSFFAKSTLIDKYDLSNLHEIASGGAPLSKEVGEAVAKRFHLP
                         GIRQGYGLTETTSAILITPEGDDKPGAVGKVVPFFEAKVVDLDTGKTLGVNQRGELCV
                         RGPMIMSGYVNNPEATNALIDKDGWLHSGDIAYWDEDEHFFIVDRLKSLIKYKGYQVA
                         PAELESILLQHPNIFDAGVAGLPDDDAGELPAAVVVLEHGKTMTEKEIVDYVASQVTT
                         AKKLRGGVVFVDEVPKGLTGKLDARKIREILIKAKKGGKIAVNSHGFPPEVEEQAAGT
                         LPMSCAQESGMDRHPAACASARINV"
         regulatory      2284..2505
                         /regulatory_class="polyA_signal_sequence"
                         /note="SV40 late poly(A) signal"
         regulatory      2553..2971
                         /regulatory_class="enhancer"
                         /note="SV40 enhancer and early promoter"
         CDS             2996..4033
                         /note="hygromycin resistance"
                         /codon_start=1
                         /transl_table=11
                         /product="hygromycin phosphotransferase"
                         /protein_id="AFM92243.1"
                         /db_xref="GI:392934105"
                         /translation="MKKPELTATSVEKFLIEKFDSVSDLMQLSEGEESRAFSFDVGGR
                         GYVLRVNSCADGFYKDRYVYRHFASAALPIPEVLDIGEFSESLTYCISRRAQGVTLQD
                         LPETELPAVLQPVAEAMDAIAAADLSQTSGFGPFGPQGIGQYTTWRDFICAIADPHVY
                         HWQTVMDDTVSASVAQALDELMLWAEDCPEVRHLVHADFGSNNVLTDNGRITAVIDWS
                         EAMFGDSQYEVANIFFWRPWLACMEQQTRYFERRHPELAGSPRLRAYMLRIGLDQLYQ
                         SLVDGNFDDAAWAQGRCDAIVRSGAGTVGRTQIARRSAAVWTDGCVEVLADSGNRRPS
                         TRPRAKEVGRV"
         regulatory      4057..4105
                         /regulatory_class="polyA_signal_sequence"
                         /note="synthetic poly(A) signal sequence"
         primer_bind     complement(4172..4191)
                         /note="RVprimer4 binding site"
         rep_origin      4429..4465
         gene            complement(5220..6080)
                         /gene="bla"
                         /note="AmpR"
         CDS             complement(5220..6080)
                         /gene="bla"
                         /note="AmpR"
                         /codon_start=1
                         /transl_table=11
                         /product="beta-lactamase"
                         /protein_id="AFM92241.1"
                         /db_xref="GI:392934103"
                         /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 gctcgtgact acgtgctgcc
          301 taggtgacta cgtgctgcct aggtgactac gtgctgccta ggtgactacg tgctgcctag
          361 ctcgaggata tcaagatctg gcctcggcgg ccaagcttag acactagagg gtatataatg
          421 gaagctcgac ttccagcttg gcaatccggt actgttggta aagccaccat ggaagatgcc
          481 aaaaacatta agaagggccc agcgccattc tacccactcg aagacgggac cgccggcgag
          541 cagctgcaca aagccatgaa gcgctacgcc ctggtgcccg gcaccatcgc ctttaccgac
          601 gcacatatcg aggtggacat tacctacgcc gagtacttcg agatgagcgt tcggctggca
          661 gaagctatga agcgctatgg gctgaataca aaccatcgga tcgtggtgtg cagcgagaat
          721 agcttgcagt tcttcatgcc cgtgttgggt gccctgttca tcggtgtggc tgtggcccca
          781 gctaacgaca tctacaacga gcgcgagctg ctgaacagca tgggcatcag ccagcccacc
          841 gtcgtattcg tgagcaagaa agggctgcaa aagatcctca acgtgcaaaa gaagctaccg
          901 atcatacaaa agatcatcat catggatagc aagaccgact accagggctt ccaaagcatg
          961 tacaccttcg tgacttccca tttgccaccc ggcttcaacg agtacgactt cgtgcccgag
         1021 agcttcgacc gggacaaaac catcgccctg atcatgaaca gtagtggcag taccggattg
         1081 cccaagggcg tagccctacc gcaccgcacc gcttgtgtcc gattcagtca tgcccgcgac
         1141 cccatcttcg gcaaccagat catccccgac accgctatcc tcagcgtggt gccatttcac
         1201 cacggcttcg gcatgttcac cacgctgggc tacttgatct gcggctttcg ggtcgtgctc
         1261 atgtaccgct tcgaggagga gctattcttg cgcagcttgc aagactataa gattcaatct
         1321 gccctgctgg tgcccacact atttagcttc ttcgctaaga gcactctcat cgacaagtac
         1381 gacctaagca acttgcacga gatcgccagc ggcggggcgc cgctcagcaa ggaggtaggt
         1441 gaggccgtgg ccaaacgctt ccacctacca ggcatccgcc agggctacgg cctgacagaa
         1501 acaaccagcg ccattctgat cacccccgaa ggggacgaca agcctggcgc agtaggcaag
         1561 gtggtgccct tcttcgaggc taaggtggtg gacttggaca ccggtaagac actgggtgtg
         1621 aaccagcgcg gcgagctgtg cgtccgtggc cccatgatca tgagcggcta cgttaacaac
         1681 cccgaggcta caaacgctct catcgacaag gacggctggc tgcacagcgg cgacatcgcc
         1741 tactgggacg aggacgagca cttcttcatc gtggaccggc tgaagagcct gatcaaatac
         1801 aagggctacc aggtagcccc agccgaactg gagagcatcc tgctgcaaca ccccaacatc
         1861 ttcgacgccg gggtcgccgg cctgcccgac gacgatgccg gcgagctgcc cgccgcagtc
         1921 gtcgtgctgg aacacggtaa aaccatgacc gagaaggaga tcgtggacta tgtggccagc
         1981 caggttacaa ccgccaagaa gctgcgcggt ggtgttgtgt tcgtggacga ggtgcctaaa
         2041 ggactgaccg gcaagttgga cgcccgcaag atccgcgaga ttctcattaa ggccaagaag
         2101 ggcggcaaga tcgccgtgaa ttctcacggc ttccctcccg aggtggagga gcaggccgcc
         2161 ggcaccctgc ccatgagctg cgcccaggag agcggcatgg atagacaccc tgctgcttgc
         2221 gccagcgcca ggatcaacgt ctaaggccgc gactctagag tcggggcggc cggccgcttc
         2281 gagcagacat gataagatac attgatgagt ttggacaaac cacaactaga atgcagtgaa
         2341 aaaaatgctt tatttgtgaa atttgtgatg ctattgcttt atttgtaacc attataagct
         2401 gcaataaaca agttaacaac aacaattgca ttcattttat gtttcaggtt cagggggagg
         2461 tgtgggaggt tttttaaagc aagtaaaacc tctacaaatg tggtaaaatc gataaggatc
         2521 cgtttgcgta ttgggcgctc ttccgctgat ctgcgcagca ccatggcctg aaataacctc
         2581 tgaaagagga acttggttag ctaccttctg aggcggaaag aaccagctgt ggaatgtgtg
         2641 tcagttaggg tgtggaaagt ccccaggctc cccagcaggc agaagtatgc aaagcatgca
         2701 tctcaattag tcagcaacca ggtgtggaaa gtccccaggc tccccagcag gcagaagtat
         2761 gcaaagcatg catctcaatt agtcagcaac catagtcccg cccctaactc cgcccatccc
         2821 gcccctaact ccgcccagtt ccgcccattc tccgccccat ggctgactaa ttttttttat
         2881 ttatgcagag gccgaggccg cctctgcctc tgagctattc cagaagtagt gaggaggctt
         2941 ttttggaggc ctaggctttt gcaaaaagct cgattcttct gacactagcg ccaccatgaa
         3001 gaagcccgaa ctcaccgcta ccagcgttga aaaatttctc atcgagaagt tcgacagtgt
         3061 gagcgacctg atgcagttgt cggagggcga agagagccga gccttcagct tcgatgtcgg
         3121 cggacgcggc tatgtactgc gggtgaatag ctgcgctgat ggcttctaca aagaccgcta
         3181 cgtgtaccgc cacttcgcca gcgctgcact acccatcccc gaagtgttgg acatcggcga
         3241 gttcagcgag agcctgacat actgcatcag tagacgcgcc caaggcgtta ctctccaaga
         3301 cctccccgaa acagagctgc ctgctgtgtt acagcctgtc gccgaagcta tggatgctat
         3361 tgccgccgcc gacctcagtc aaaccagcgg cttcggccca ttcgggcccc aaggcatcgg
         3421 ccagtacaca acctggcggg atttcatttg cgccattgct gatccccatg tctaccactg
         3481 gcagaccgtg atggacgaca ccgtgtccgc cagcgtagct caagccctgg acgaactgat
         3541 gctgtgggcc gaagactgtc ccgaggtgcg ccacctcgtc catgccgact tcggcagcaa
         3601 caacgtcctg accgacaacg gccgcatcac cgccgtaatc gactggtccg aagctatgtt
         3661 cggggacagt cagtacgagg tggccaacat cttcttctgg cggccctggc tggcttgcat
         3721 ggagcagcag actcgctact tcgagcgccg gcatcccgag ctggccggca gccctcgtct
         3781 gcgagcctac atgctgcgca tcggcctgga tcagctctac cagagcctcg tggacggcaa
         3841 cttcgacgat gctgcctggg ctcaaggccg ctgcgatgcc atcgtccgca gcggggccgg
         3901 caccgtcggt cgcacacaaa tcgctcgccg gagcgcagcc gtatggaccg acggctgcgt
         3961 cgaggtgctg gccgacagcg gcaaccgccg gcccagtaca cgaccgcgcg ctaaggaggt
         4021 aggtcgagtt taaactctag aaccggtcat ggccgcaata aaatatcttt attttcatta
         4081 catctgtgtg ttggtttttt gtgtgttcga actagatgct gtcgaccgat gcccttgaga
         4141 gccttcaacc cagtcagctc cttccggtgg gcgcggggca tgactatcgt cgccgcactt
         4201 atgactgtct tctttatcat gcaactcgta ggacaggtgc cggcagcgct cttccgcttc
         4261 ctcgctcact gactcgctgc gctcggtcgt tcggctgcgg cgagcggtat cagctcactc
         4321 aaaggcggta atacggttat ccacagaatc aggggataac gcaggaaaga acatgtgagc
         4381 aaaaggccag caaaaggcca ggaaccgtaa aaaggccgcg ttgctggcgt ttttccatag
         4441 gctccgcccc cctgacgagc atcacaaaaa tcgacgctca agtcagaggt ggcgaaaccc
         4501 gacaggacta taaagatacc aggcgtttcc ccctggaagc tccctcgtgc gctctcctgt
         4561 tccgaccctg ccgcttaccg gatacctgtc cgcctttctc ccttcgggaa gcgtggcgct
         4621 ttctcatagc tcacgctgta ggtatctcag ttcggtgtag gtcgttcgct ccaagctggg
         4681 ctgtgtgcac gaaccccccg ttcagcccga ccgctgcgcc ttatccggta actatcgtct
         4741 tgagtccaac ccggtaagac acgacttatc gccactggca gcagccactg gtaacaggat
         4801 tagcagagcg aggtatgtag gcggtgctac agagttcttg aagtggtggc ctaactacgg
         4861 ctacactaga agaacagtat ttggtatctg cgctctgctg aagccagtta ccttcggaaa
         4921 aagagttggt agctcttgat ccggcaaaca aaccaccgct ggtagcggtg gtttttttgt
         4981 ttgcaagcag cagattacgc gcagaaaaaa aggatctcaa gaagatcctt tgatcttttc
         5041 tacggggtct gacgctcagt ggaacgaaaa ctcacgttaa gggattttgg tcatgagatt
         5101 atcaaaaagg atcttcacct agatcctttt aaattaaaaa tgaagtttta aatcaatcta
         5161 aagtatatat gagtaaactt ggtctgacag cggccgcaaa tgctaaacca ctgcagtggt
         5221 taccagtgct tgatcagtga ggcaccgatc tcagcgatct gcctatttcg ttcgtccata
         5281 gtggcctgac tccccgtcgt gtagatcact acgattcgtg agggcttacc atcaggcccc
         5341 agcgcagcaa tgatgccgcg agagccgcgt tcaccggccc ccgatttgtc agcaatgaac
         5401 cagccagcag ggagggccga gcgaagaagt ggtcctgcta ctttgtccgc ctccatccag
         5461 tctatgagct gctgtcgtga tgctagagta agaagttcgc cagtgagtag tttccgaaga
         5521 gttgtggcca ttgctactgg catcgtggta tcacgctcgt cgttcggtat ggcttcgttc
         5581 aactctggtt cccagcggtc aagccgggtc acatgatcac ccatattatg aagaaatgca
         5641 gtcagctcct tagggcctcc gatcgttgtc agaagtaagt tggccgcggt gttgtcgctc
         5701 atggtaatgg cagcactaca caattctctt accgtcatgc catccgtaag atgcttttcc
         5761 gtgaccggcg agtactcaac caagtcgttt tgtgagtagt gtatacggcg accaagctgc
         5821 tcttgcccgg cgtctatacg ggacaacacc gcgccacata gcagtacttt gaaagtgctc
         5881 atcatcggga atcgttcttc ggggcggaaa gactcaagga tcttgccgct attgagatcc
         5941 agttcgatat agcccactct tgcacccagt tgatcttcag catcttttac tttcaccagc
         6001 gtttcggggt gtgcaaaaac aggcaagcaa aatgccgcaa agaagggaat gagtgcgaca
         6061 cgaaaatgtt ggatgctcat

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