e. coli xl1-blue cells Search Results


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  • 96
    Stratagene e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Agilent technologies e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Thermo Fisher e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene competent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Agilent technologies competent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Millipore competent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Thermo Fisher electrocompetent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene electrocompetent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Millipore e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene supercompetent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Thermo Fisher competent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene ultracompetent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Agilent technologies electrocompetent e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene log phase e coli xl1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
    Log Phase E Coli Xl1 Blue Cells, supplied by Stratagene, used in various techniques. Bioz Stars score: 79/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Stratagene e coli xl1 blue p2 cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Agilent technologies e coli xl1 blue supercompetent cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene e coli xl1 blue mrf cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene e coli xl1 blue mrf host cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
    E Coli Xl1 Blue Mrf Host Cells, supplied by Stratagene, used in various techniques. Bioz Stars score: 78/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Stratagene competent e coli xl1 blue mrf cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
    Competent E Coli Xl1 Blue Mrf Cells, supplied by Stratagene, used in various techniques. Bioz Stars score: 80/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Stratagene electrocompetent e coli xl1 blue mrf cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Agilent technologies e coli xl1 blue electroporation competent cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    TaKaRa infected e coli xl1 blue bacterial cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Millipore e coli xl1 blue supercompetent cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
    E Coli Xl1 Blue Supercompetent Cells, supplied by Millipore, used in various techniques. Bioz Stars score: 81/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies e coli xl1 blue chemical competent cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene e coli xl1 blue strain
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Becton Dickinson e coli xl1 blue
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Agilent technologies xl1 blue e scheri chia coli competent cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    TaKaRa log phase xl1 blue e coli cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene chemical competent e coli xl 1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene e coli strain xl1 blue mrf cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Stratagene heat competent e coli xl 1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    TaKaRa e coli xl 1 blue cells
    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli <t>XL1</t> Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.
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    Image Search Results


    Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli XL1 Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.

    Journal: Immunology

    Article Title: Phage display of human antibodies from a patient suffering from coeliac disease and selection of isotype-specific scFv against gliadin

    doi: 10.1046/j.1365-2567.2003.01728.x

    Figure Lengend Snippet: Isotype-specific phage enrichment during subsequent rounds of affinity selection. The number of phage was determined as colony-forming units (CFU) after infection of freshly grown Escherichia coli XL1 Blue cells. Notably, the absolute number of eluted phage significantly depends on the isotype library used for screening.

    Article Snippet: Nine different isotype-specific ligation mixtures were used for transformation of E. coli XL1 Blue cells (Stratagene, LaJolla, CA) yielding libraries containing between 1 × 107 and 5 × 108 primary clones.

    Techniques: Selection, Infection

    Low-temperature growth of E. coli transformants harboring the icdII gene. (Upper panel) E. coli XL1-Blue was transformed with pMSF8 or pMS42. (Lower panel) E. coli DEK2004 was used as the host and transformed with the indicated plasmid. pBluescript was used as a vector. E. coli transformants harboring each plasmid were streaked on MOPS-succinate or MOPS-succinate-yeast extract agar plates and incubated at 10 or 15°C. Photographs were taken 2 weeks after the inoculation.

    Journal: Journal of Bacteriology

    Article Title: cis-Acting Elements Responsible for Low-Temperature-Inducible Expression of the Gene Coding for the Thermolabile Isocitrate Dehydrogenase Isozyme of a Psychrophilic Bacterium, Vibrio sp. Strain ABE-1

    doi:

    Figure Lengend Snippet: Low-temperature growth of E. coli transformants harboring the icdII gene. (Upper panel) E. coli XL1-Blue was transformed with pMSF8 or pMS42. (Lower panel) E. coli DEK2004 was used as the host and transformed with the indicated plasmid. pBluescript was used as a vector. E. coli transformants harboring each plasmid were streaked on MOPS-succinate or MOPS-succinate-yeast extract agar plates and incubated at 10 or 15°C. Photographs were taken 2 weeks after the inoculation.

    Article Snippet: E. coli DEK2004, a mutant defective in icd (a gift from Peter Thorsness), or E. coli XL1-Blue (Stratagene) was used as a host for transformation by icd genes.

    Techniques: Transformation Assay, Plasmid Preparation, Incubation

    Growth of E. coli transformants harboring 5′-deleted icdII or an icdII-icdI fusion gene. (A) E. coli DEK2004 was transformed with vector [pBluescript KS(+)] (○), pMS42 (▿), pIS202 (▴), or pMSF8 (▵). (B) E. coli DEK2004 was transformed with pTS601 (⧫), pTS602 (◊), or pSS512 (□). As a control, E. coli XL1-Blue, which has its own icd gene, was also transformed with the vector (●). Other symbols are the same as in panel A. Each transformant, precultured in LB medium at 37°C for 16 h, was inoculated in fresh LB medium and cultured at 15 or 37°C. (C) Specific activity of IDH determined with crude extract prepared from each transformant. Details of assay conditions are described in Materials and Methods. Note the thermolability of IDH-II at 37°C.

    Journal: Journal of Bacteriology

    Article Title: cis-Acting Elements Responsible for Low-Temperature-Inducible Expression of the Gene Coding for the Thermolabile Isocitrate Dehydrogenase Isozyme of a Psychrophilic Bacterium, Vibrio sp. Strain ABE-1

    doi:

    Figure Lengend Snippet: Growth of E. coli transformants harboring 5′-deleted icdII or an icdII-icdI fusion gene. (A) E. coli DEK2004 was transformed with vector [pBluescript KS(+)] (○), pMS42 (▿), pIS202 (▴), or pMSF8 (▵). (B) E. coli DEK2004 was transformed with pTS601 (⧫), pTS602 (◊), or pSS512 (□). As a control, E. coli XL1-Blue, which has its own icd gene, was also transformed with the vector (●). Other symbols are the same as in panel A. Each transformant, precultured in LB medium at 37°C for 16 h, was inoculated in fresh LB medium and cultured at 15 or 37°C. (C) Specific activity of IDH determined with crude extract prepared from each transformant. Details of assay conditions are described in Materials and Methods. Note the thermolability of IDH-II at 37°C.

    Article Snippet: E. coli DEK2004, a mutant defective in icd (a gift from Peter Thorsness), or E. coli XL1-Blue (Stratagene) was used as a host for transformation by icd genes.

    Techniques: Transformation Assay, Plasmid Preparation, Cell Culture, Activity Assay