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lysogeny broth lb medium  (Thermo Fisher)


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    Thermo Fisher lysogeny broth lb medium
    Lysogeny Broth Lb Medium, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lb+broth+medium/Ampicillin/pm42337800-79-20-27
    Average 99 stars, based on 1 article reviews
    lysogeny broth lb medium - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Bacteria:

    Article Title: Action of 3-Hydroxy-3-Methylglutaryl-CoA Reductase Inhibitors on ABCA-1 protein (ATP-Binding Cassette Transporter-1) in endothelial cells stimulated with uremic serum.
    Article Snippet: The bacteria were then plated on LB Agar medium (Luria Bertani) (Sigma-Aldrich, USA) supplemented with 100 μg/mL ampicillin (Gibco, USA) and incubated for 24 h at 37oC with 5% CO2 saturation. .. After colony growth, bacteria were cultured in LB Broth medium supplemented with 100 μg/mL ampicillin and incubated at 37oC with shaking at 120 rpm for 24 h. Plasmid DNA was then extracted and purified using the QIAprep Spin kit (Qiagen, Germany), quantified using a Nanodrop, and stored at −20oC. ..

    Article Title: Interfacial water confers transcription factors with dinucleotide specificity.
    Article Snippet: The pETG20A_SPB vectors with BARHL2 and its mutant sequences (GenScript) were expressed in Rosetta(DE3)pLysS E. coli strain (Millipore). .. In brief, the bacteria were grown overnight at 37 °C in LB Broth medium (Gibco) with carbenicillin (0.1 mg ml−1) and chloramphenicol (34 μg ml−1) and then transferred to the induction medium consisting of the previous medium with additional reagents at the following final concentrations: 1 mM MgSO4, metal mixture (50 μM FeCl3, 20 μM CaCl3, 10 μM each of MgCl2 and ZnSO4, 2 μM each of CoCl2, CuCl2, NiCl2, Na2MoO4, Na2SeO3 and H3BO3), 60 μM HCl, NPS (50 mM KH2PO4, 50 mM Na2HPO4, 25 mM (NH4)2SO4) and 5052 (0.5% glycerol, 0.05% glucose and 0.2% alpha-lactose)94. ..

    Article Title: Oligonucleotide agonists targeting progranulin
    Article Snippet: GRN 5′ UTR Luciferase Reporter Constructs The GRN 5′ UTR sequence (SEQ ID #690) was cloned into the psiCHECK2 plasmid (Promega) immediately in front of the renilla luciferase ATG site using the Q5 site-directed mutagenesis kit (New England Biolabs) according to manufacturer's instruction. .. 5′ UTR sequence from nucleotide number 38 to 256 according to Homo sapiens granulin precursor (GRN), RefSeq NM_002087.3 (SEQ ID NO 1): SEQ 690 ID#GGCGAGAGGAAGCAGGGAGGAGAGTGATTTGAGTAGAAAAGAAACAC AGCATTCCAGGCTGGCCCCACCTCTATATTGATAAGTAGCCAATGGGAGC GGGTAGCCCTGATCCCTGGCCAATGGAAACTGAGGTAGGCGGGTCATCGC GCTGGGGTCTGTAGTCTGAGCGCTACCCGGTTGCTGCTGCCCAAGGACCG CGGAGTCGGACGCAGGCAGACC For the site-directed mutagenesis and insertion of the GRN 5′ UTR the following primers were used: Forward primer SEQ ID NO 691 5′-ATGGAAACTGAGGTAGGCGGGTCATCGCGCTGGGGTCTGTAGTCTGA GCGCTACCCGGTTGCTGCTGCCCAAGGACCGCGGAGTCGGACGCAGGCAG ACCATGGCTTCCAAGGTGTACGACCCCGAGC-3′ and reverse primer SEQ ID NO 692 5′-TGGCCAGGGATCAGGGCTACCCGCTCCCATTGGCTACTTATCAATAT AGAGGTGGGGCCAGCCTGGAATGCTGTGTTTCTTTTCTACTCAAATCACT CTCCTCCCTGCTTCCTCTCGCCGGCTAGCCTATAGTGAGTCGTATTAAGT AC After transformation of chemical competent bacteria (One Shot TOP10 Chemically Competent E. coli, Thermofisher) and overnight growth on LB agar plates containing ampicillin (imMedia Growth Medium, agar, ampicillin, Thermofisher), single colonies were selected and further grown overnight with constant shaking at 37 Degrees Celcius in LB broth medium containing ampicillin (50 μg/mL) (Thermofisher). .. Final mini- and midi-prep plasmid purifications were done according to vendors instruction (Qiagen).

    Article Title: Oligonucleotide agonists targeting progranulin
    Article Snippet: SEQ ID#2: GGGACAGTACTGAAGACTCTGCAGCCCTCGGGACCCCACTCGGAGGGTGC CCTCTGCTCAGGCCTCCCTAGACCTCCCCCTAACCAAATTCTCCCTGGAC CCCATTCTGAGCTCCCCATCACCATGGGAGGTGGGGCCTCAATCTAAGGC CTTCCCTGTCAGAAGGGGGTTGTGGCAAAAGCCACATTACAAGCTGCCAT CCCCTCCCCGTTTCAGTGGACCCTGTGGCCAGGTGCTTTTCCCTATCCAC AGGGGTGTTTGTGTGTGTGCGCGTGTGCGTTTCAATAAAGTTTGTACACT TTCTTAA Double stranded DNA fragment (gBlock, Integrated DNA technologies) containing the GRN 3′ UTR (SEQ ID #2) flanked by XhoI and NotI sites was cut by XhoI and NotI enzymes (New England Biolabs) according to vendors protocol and ligated using T4 Ligase (New England Biolabs) into the previously XhoI/NotI cut psiCHECK2 plasmid. .. After transformation of chemical competent bacteria (One Shot® TOP10 Chemically Competent E. coli, Thermofisher) and overnight growth on LB agar plates containing ampicillin (imMedia Growth Medium, agar, ampicillin, Thermofisher), single colonies were selected and further grown overnight with constant shaking at 37 Degrees Celcius in LB broth medium containing ampicillin (50 μg/mL) (Thermofisher). .. Final mini- and midiprep plasmid purifications were done according to vendors instruction (Qiagen).

    Cell Culture:

    Article Title: Action of 3-Hydroxy-3-Methylglutaryl-CoA Reductase Inhibitors on ABCA-1 protein (ATP-Binding Cassette Transporter-1) in endothelial cells stimulated with uremic serum.
    Article Snippet: The bacteria were then plated on LB Agar medium (Luria Bertani) (Sigma-Aldrich, USA) supplemented with 100 μg/mL ampicillin (Gibco, USA) and incubated for 24 h at 37oC with 5% CO2 saturation. .. After colony growth, bacteria were cultured in LB Broth medium supplemented with 100 μg/mL ampicillin and incubated at 37oC with shaking at 120 rpm for 24 h. Plasmid DNA was then extracted and purified using the QIAprep Spin kit (Qiagen, Germany), quantified using a Nanodrop, and stored at −20oC. ..

    Incubation:

    Article Title: Action of 3-Hydroxy-3-Methylglutaryl-CoA Reductase Inhibitors on ABCA-1 protein (ATP-Binding Cassette Transporter-1) in endothelial cells stimulated with uremic serum.
    Article Snippet: The bacteria were then plated on LB Agar medium (Luria Bertani) (Sigma-Aldrich, USA) supplemented with 100 μg/mL ampicillin (Gibco, USA) and incubated for 24 h at 37oC with 5% CO2 saturation. .. After colony growth, bacteria were cultured in LB Broth medium supplemented with 100 μg/mL ampicillin and incubated at 37oC with shaking at 120 rpm for 24 h. Plasmid DNA was then extracted and purified using the QIAprep Spin kit (Qiagen, Germany), quantified using a Nanodrop, and stored at −20oC. ..

    Article Title: Significance of zinc-solubilizing plant growth-promoting rhizobacterial strains in nutrient acquisition, enhancement of growth, yield, and oil content of canola ( Brassica napus L.)
    Article Snippet: .. Each strain cultures were incubated in 5 ml of LB broth medium at 28°C for 48 h, after which 20 μl of culture cells were placed in salt minimal media enriched with and without L-tryptophan (5 mg L −1 ) at 28°C for 48 h on an orbital shaker (Thermo Scientific TM , MaxQ TM , 40,000 ® ). ..

    Plasmid Preparation:

    Article Title: Action of 3-Hydroxy-3-Methylglutaryl-CoA Reductase Inhibitors on ABCA-1 protein (ATP-Binding Cassette Transporter-1) in endothelial cells stimulated with uremic serum.
    Article Snippet: The bacteria were then plated on LB Agar medium (Luria Bertani) (Sigma-Aldrich, USA) supplemented with 100 μg/mL ampicillin (Gibco, USA) and incubated for 24 h at 37oC with 5% CO2 saturation. .. After colony growth, bacteria were cultured in LB Broth medium supplemented with 100 μg/mL ampicillin and incubated at 37oC with shaking at 120 rpm for 24 h. Plasmid DNA was then extracted and purified using the QIAprep Spin kit (Qiagen, Germany), quantified using a Nanodrop, and stored at −20oC. ..

    Purification:

    Article Title: Action of 3-Hydroxy-3-Methylglutaryl-CoA Reductase Inhibitors on ABCA-1 protein (ATP-Binding Cassette Transporter-1) in endothelial cells stimulated with uremic serum.
    Article Snippet: The bacteria were then plated on LB Agar medium (Luria Bertani) (Sigma-Aldrich, USA) supplemented with 100 μg/mL ampicillin (Gibco, USA) and incubated for 24 h at 37oC with 5% CO2 saturation. .. After colony growth, bacteria were cultured in LB Broth medium supplemented with 100 μg/mL ampicillin and incubated at 37oC with shaking at 120 rpm for 24 h. Plasmid DNA was then extracted and purified using the QIAprep Spin kit (Qiagen, Germany), quantified using a Nanodrop, and stored at −20oC. ..

    Article Title: Completely noninvasive multi-analyte monitoring system for cell culture processes
    Article Snippet: .. The LB broth medium was prepared by suspending 20 g of LB broth powder (Thermo Fisher Scientific, Waltham, MA, USA) in 1 L purified water. ..

    Control:

    Article Title: Biological amelioration of water stress in rapeseed ( Brassica napus L.) by exopolysaccharides‐producing Pseudomonas protegens ML15
    Article Snippet: .. An overnight liquid culture of each isolate (2%, v/v) was inoculated into LB broth medium supplemented with and without the addition of PEG‐6000 (ThermoFisher; 24% w/v) to induce drought stress, with the medium without PEG‐6000 serving as the control. ..

    Article Title: Biological amelioration of water stress in rapeseed (Brassica napus L.) by exopolysaccharides-producing Pseudomonas protegens ML15.
    Article Snippet: .. An overnight liquid culture of each isolate (2%, v/v) was inoculated into LB broth medium supplemented with and without the addition of PEG-6000 (ThermoFisher; 24% w/v) to induce drought stress, with the medium without PEG-6000 serving as the control. ..

    Sequencing:

    Article Title: Oligonucleotide agonists targeting progranulin
    Article Snippet: GRN 5′ UTR Luciferase Reporter Constructs The GRN 5′ UTR sequence (SEQ ID #690) was cloned into the psiCHECK2 plasmid (Promega) immediately in front of the renilla luciferase ATG site using the Q5 site-directed mutagenesis kit (New England Biolabs) according to manufacturer's instruction. .. 5′ UTR sequence from nucleotide number 38 to 256 according to Homo sapiens granulin precursor (GRN), RefSeq NM_002087.3 (SEQ ID NO 1): SEQ 690 ID#GGCGAGAGGAAGCAGGGAGGAGAGTGATTTGAGTAGAAAAGAAACAC AGCATTCCAGGCTGGCCCCACCTCTATATTGATAAGTAGCCAATGGGAGC GGGTAGCCCTGATCCCTGGCCAATGGAAACTGAGGTAGGCGGGTCATCGC GCTGGGGTCTGTAGTCTGAGCGCTACCCGGTTGCTGCTGCCCAAGGACCG CGGAGTCGGACGCAGGCAGACC For the site-directed mutagenesis and insertion of the GRN 5′ UTR the following primers were used: Forward primer SEQ ID NO 691 5′-ATGGAAACTGAGGTAGGCGGGTCATCGCGCTGGGGTCTGTAGTCTGA GCGCTACCCGGTTGCTGCTGCCCAAGGACCGCGGAGTCGGACGCAGGCAG ACCATGGCTTCCAAGGTGTACGACCCCGAGC-3′ and reverse primer SEQ ID NO 692 5′-TGGCCAGGGATCAGGGCTACCCGCTCCCATTGGCTACTTATCAATAT AGAGGTGGGGCCAGCCTGGAATGCTGTGTTTCTTTTCTACTCAAATCACT CTCCTCCCTGCTTCCTCTCGCCGGCTAGCCTATAGTGAGTCGTATTAAGT AC After transformation of chemical competent bacteria (One Shot TOP10 Chemically Competent E. coli, Thermofisher) and overnight growth on LB agar plates containing ampicillin (imMedia Growth Medium, agar, ampicillin, Thermofisher), single colonies were selected and further grown overnight with constant shaking at 37 Degrees Celcius in LB broth medium containing ampicillin (50 μg/mL) (Thermofisher). .. Final mini- and midi-prep plasmid purifications were done according to vendors instruction (Qiagen).

    Mutagenesis:

    Article Title: Oligonucleotide agonists targeting progranulin
    Article Snippet: GRN 5′ UTR Luciferase Reporter Constructs The GRN 5′ UTR sequence (SEQ ID #690) was cloned into the psiCHECK2 plasmid (Promega) immediately in front of the renilla luciferase ATG site using the Q5 site-directed mutagenesis kit (New England Biolabs) according to manufacturer's instruction. .. 5′ UTR sequence from nucleotide number 38 to 256 according to Homo sapiens granulin precursor (GRN), RefSeq NM_002087.3 (SEQ ID NO 1): SEQ 690 ID#GGCGAGAGGAAGCAGGGAGGAGAGTGATTTGAGTAGAAAAGAAACAC AGCATTCCAGGCTGGCCCCACCTCTATATTGATAAGTAGCCAATGGGAGC GGGTAGCCCTGATCCCTGGCCAATGGAAACTGAGGTAGGCGGGTCATCGC GCTGGGGTCTGTAGTCTGAGCGCTACCCGGTTGCTGCTGCCCAAGGACCG CGGAGTCGGACGCAGGCAGACC For the site-directed mutagenesis and insertion of the GRN 5′ UTR the following primers were used: Forward primer SEQ ID NO 691 5′-ATGGAAACTGAGGTAGGCGGGTCATCGCGCTGGGGTCTGTAGTCTGA GCGCTACCCGGTTGCTGCTGCCCAAGGACCGCGGAGTCGGACGCAGGCAG ACCATGGCTTCCAAGGTGTACGACCCCGAGC-3′ and reverse primer SEQ ID NO 692 5′-TGGCCAGGGATCAGGGCTACCCGCTCCCATTGGCTACTTATCAATAT AGAGGTGGGGCCAGCCTGGAATGCTGTGTTTCTTTTCTACTCAAATCACT CTCCTCCCTGCTTCCTCTCGCCGGCTAGCCTATAGTGAGTCGTATTAAGT AC After transformation of chemical competent bacteria (One Shot TOP10 Chemically Competent E. coli, Thermofisher) and overnight growth on LB agar plates containing ampicillin (imMedia Growth Medium, agar, ampicillin, Thermofisher), single colonies were selected and further grown overnight with constant shaking at 37 Degrees Celcius in LB broth medium containing ampicillin (50 μg/mL) (Thermofisher). .. Final mini- and midi-prep plasmid purifications were done according to vendors instruction (Qiagen).

    Transformation Assay:

    Article Title: Oligonucleotide agonists targeting progranulin
    Article Snippet: GRN 5′ UTR Luciferase Reporter Constructs The GRN 5′ UTR sequence (SEQ ID #690) was cloned into the psiCHECK2 plasmid (Promega) immediately in front of the renilla luciferase ATG site using the Q5 site-directed mutagenesis kit (New England Biolabs) according to manufacturer's instruction. .. 5′ UTR sequence from nucleotide number 38 to 256 according to Homo sapiens granulin precursor (GRN), RefSeq NM_002087.3 (SEQ ID NO 1): SEQ 690 ID#GGCGAGAGGAAGCAGGGAGGAGAGTGATTTGAGTAGAAAAGAAACAC AGCATTCCAGGCTGGCCCCACCTCTATATTGATAAGTAGCCAATGGGAGC GGGTAGCCCTGATCCCTGGCCAATGGAAACTGAGGTAGGCGGGTCATCGC GCTGGGGTCTGTAGTCTGAGCGCTACCCGGTTGCTGCTGCCCAAGGACCG CGGAGTCGGACGCAGGCAGACC For the site-directed mutagenesis and insertion of the GRN 5′ UTR the following primers were used: Forward primer SEQ ID NO 691 5′-ATGGAAACTGAGGTAGGCGGGTCATCGCGCTGGGGTCTGTAGTCTGA GCGCTACCCGGTTGCTGCTGCCCAAGGACCGCGGAGTCGGACGCAGGCAG ACCATGGCTTCCAAGGTGTACGACCCCGAGC-3′ and reverse primer SEQ ID NO 692 5′-TGGCCAGGGATCAGGGCTACCCGCTCCCATTGGCTACTTATCAATAT AGAGGTGGGGCCAGCCTGGAATGCTGTGTTTCTTTTCTACTCAAATCACT CTCCTCCCTGCTTCCTCTCGCCGGCTAGCCTATAGTGAGTCGTATTAAGT AC After transformation of chemical competent bacteria (One Shot TOP10 Chemically Competent E. coli, Thermofisher) and overnight growth on LB agar plates containing ampicillin (imMedia Growth Medium, agar, ampicillin, Thermofisher), single colonies were selected and further grown overnight with constant shaking at 37 Degrees Celcius in LB broth medium containing ampicillin (50 μg/mL) (Thermofisher). .. Final mini- and midi-prep plasmid purifications were done according to vendors instruction (Qiagen).

    Article Title: Oligonucleotide agonists targeting progranulin
    Article Snippet: SEQ ID#2: GGGACAGTACTGAAGACTCTGCAGCCCTCGGGACCCCACTCGGAGGGTGC CCTCTGCTCAGGCCTCCCTAGACCTCCCCCTAACCAAATTCTCCCTGGAC CCCATTCTGAGCTCCCCATCACCATGGGAGGTGGGGCCTCAATCTAAGGC CTTCCCTGTCAGAAGGGGGTTGTGGCAAAAGCCACATTACAAGCTGCCAT CCCCTCCCCGTTTCAGTGGACCCTGTGGCCAGGTGCTTTTCCCTATCCAC AGGGGTGTTTGTGTGTGTGCGCGTGTGCGTTTCAATAAAGTTTGTACACT TTCTTAA Double stranded DNA fragment (gBlock, Integrated DNA technologies) containing the GRN 3′ UTR (SEQ ID #2) flanked by XhoI and NotI sites was cut by XhoI and NotI enzymes (New England Biolabs) according to vendors protocol and ligated using T4 Ligase (New England Biolabs) into the previously XhoI/NotI cut psiCHECK2 plasmid. .. After transformation of chemical competent bacteria (One Shot® TOP10 Chemically Competent E. coli, Thermofisher) and overnight growth on LB agar plates containing ampicillin (imMedia Growth Medium, agar, ampicillin, Thermofisher), single colonies were selected and further grown overnight with constant shaking at 37 Degrees Celcius in LB broth medium containing ampicillin (50 μg/mL) (Thermofisher). .. Final mini- and midiprep plasmid purifications were done according to vendors instruction (Qiagen).



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