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e coli ifo 3301 b subtilis atcc 6633 qbeta atcc 23 631 b1 l pneumophila atcc 33 152 p aeruginosa atcc  (ATCC)


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    ATCC e coli ifo 3301 b subtilis atcc 6633 qbeta atcc 23 631 b1 l pneumophila atcc 33 152 p aeruginosa atcc
    Summary of UV based inactivation studies.
    E Coli Ifo 3301 B Subtilis Atcc 6633 Qbeta Atcc 23 631 B1 L Pneumophila Atcc 33 152 P Aeruginosa Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1323 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/e coli ifo 3301 b subtilis atcc 6633 qbeta atcc 23 631 b1 l pneumophila atcc 33 152 p aeruginosa atcc/product/ATCC
    Average 99 stars, based on 1323 article reviews
    e coli ifo 3301 b subtilis atcc 6633 qbeta atcc 23 631 b1 l pneumophila atcc 33 152 p aeruginosa atcc - by Bioz Stars, 2026-04
    99/100 stars

    Images

    1) Product Images from "A critical review of ultra-violet light emitting diodes as a one water disinfection technology"

    Article Title: A critical review of ultra-violet light emitting diodes as a one water disinfection technology

    Journal: Water Research X

    doi: 10.1016/j.wroa.2024.100271

    Summary of UV based inactivation studies.
    Figure Legend Snippet: Summary of UV based inactivation studies.

    Techniques Used:

    Reported Inactivation Constants for E. coli Species. Shapes Represent Lamp Source and Colour Represent Measured Incident Intensity of the System. Note That Composition and Depth of the Matrix Will Dictate Delivered Dose.
    Figure Legend Snippet: Reported Inactivation Constants for E. coli Species. Shapes Represent Lamp Source and Colour Represent Measured Incident Intensity of the System. Note That Composition and Depth of the Matrix Will Dictate Delivered Dose.

    Techniques Used:

    Summary table for UV LED flow-through studies.
    Figure Legend Snippet: Summary table for UV LED flow-through studies.

    Techniques Used:



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    Panel A) wild type Qβ phages; Panel B) Qβ-FMDV VP1 G-H loop phages; Panel C) Qβ-GFP rescued phages from <t>E.</t> <t>coli</t> SURE (expression host with F + ) over-expressing A1-GFP protein infected with wild type Qβ. Panel D) QβΔA1 phages. All at very low multiplicity of infection (MOI), and all plates are exactly 1 day (24 hours) old when photographed.
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    Image Search Results


    Summary of UV based inactivation studies.

    Journal: Water Research X

    Article Title: A critical review of ultra-violet light emitting diodes as a one water disinfection technology

    doi: 10.1016/j.wroa.2024.100271

    Figure Lengend Snippet: Summary of UV based inactivation studies.

    Article Snippet: Synthetic , CB , 253.7 (LP) 265 280 300 , E. coli IFO 3301 B. subtilis ATCC 6633 QBeta ATCC 23,631 B1 L. pneumophila ATCC 33,152 P. aeruginosa ATCC 10,145 , ( ) .

    Techniques:

    Reported Inactivation Constants for E. coli Species. Shapes Represent Lamp Source and Colour Represent Measured Incident Intensity of the System. Note That Composition and Depth of the Matrix Will Dictate Delivered Dose.

    Journal: Water Research X

    Article Title: A critical review of ultra-violet light emitting diodes as a one water disinfection technology

    doi: 10.1016/j.wroa.2024.100271

    Figure Lengend Snippet: Reported Inactivation Constants for E. coli Species. Shapes Represent Lamp Source and Colour Represent Measured Incident Intensity of the System. Note That Composition and Depth of the Matrix Will Dictate Delivered Dose.

    Article Snippet: Synthetic , CB , 253.7 (LP) 265 280 300 , E. coli IFO 3301 B. subtilis ATCC 6633 QBeta ATCC 23,631 B1 L. pneumophila ATCC 33,152 P. aeruginosa ATCC 10,145 , ( ) .

    Techniques:

    Summary table for UV LED flow-through studies.

    Journal: Water Research X

    Article Title: A critical review of ultra-violet light emitting diodes as a one water disinfection technology

    doi: 10.1016/j.wroa.2024.100271

    Figure Lengend Snippet: Summary table for UV LED flow-through studies.

    Article Snippet: Synthetic , CB , 253.7 (LP) 265 280 300 , E. coli IFO 3301 B. subtilis ATCC 6633 QBeta ATCC 23,631 B1 L. pneumophila ATCC 33,152 P. aeruginosa ATCC 10,145 , ( ) .

    Techniques:

    Panel A) wild type Qβ phages; Panel B) Qβ-FMDV VP1 G-H loop phages; Panel C) Qβ-GFP rescued phages from E. coli SURE (expression host with F + ) over-expressing A1-GFP protein infected with wild type Qβ. Panel D) QβΔA1 phages. All at very low multiplicity of infection (MOI), and all plates are exactly 1 day (24 hours) old when photographed.

    Journal: PLoS ONE

    Article Title: In Vitro Evolution and Affinity-Maturation with Coliphage Qβ Display

    doi: 10.1371/journal.pone.0113069

    Figure Lengend Snippet: Panel A) wild type Qβ phages; Panel B) Qβ-FMDV VP1 G-H loop phages; Panel C) Qβ-GFP rescued phages from E. coli SURE (expression host with F + ) over-expressing A1-GFP protein infected with wild type Qβ. Panel D) QβΔA1 phages. All at very low multiplicity of infection (MOI), and all plates are exactly 1 day (24 hours) old when photographed.

    Article Snippet: The E. coli bacteriophage Q-β ATCC 23631-B1 was used as a positive wild type (wt) control in experiments.

    Techniques: Expressing, Infection

    A) A population of phages displaying the library of interest (here randomized VP1 G-H loop) was added to the well of a plate pre-coated with the desired target (in this case, mAb SD6 covalently immobilized with F c region). B) Indicator E coli are added to the well after phages having low-affinity to the target are removed. C) High-affinity phage bound to target can infect E. coli Q13 by adsorbing and injecting its RNA via the F + pilus. D) Phages newly obtained after indicator E. coli infection were transferred to new wells containing the immobilized target for the next round of biopanning.

    Journal: PLoS ONE

    Article Title: In Vitro Evolution and Affinity-Maturation with Coliphage Qβ Display

    doi: 10.1371/journal.pone.0113069

    Figure Lengend Snippet: A) A population of phages displaying the library of interest (here randomized VP1 G-H loop) was added to the well of a plate pre-coated with the desired target (in this case, mAb SD6 covalently immobilized with F c region). B) Indicator E coli are added to the well after phages having low-affinity to the target are removed. C) High-affinity phage bound to target can infect E. coli Q13 by adsorbing and injecting its RNA via the F + pilus. D) Phages newly obtained after indicator E. coli infection were transferred to new wells containing the immobilized target for the next round of biopanning.

    Article Snippet: The E. coli bacteriophage Q-β ATCC 23631-B1 was used as a positive wild type (wt) control in experiments.

    Techniques: Infection

    Table adapted from Drake <xref ref-type= [29] ." width="100%" height="100%">

    Journal: PLoS ONE

    Article Title: In Vitro Evolution and Affinity-Maturation with Coliphage Qβ Display

    doi: 10.1371/journal.pone.0113069

    Figure Lengend Snippet: Table adapted from Drake [29] .

    Article Snippet: The E. coli bacteriophage Q-β ATCC 23631-B1 was used as a positive wild type (wt) control in experiments.

    Techniques: