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e coli bacteriophage qβ  (ATCC)


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    Structured Review

    ATCC e coli bacteriophage qβ
    E Coli Bacteriophage Qβ, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/e coli bacteriophage qβ/product/ATCC
    Average 93 stars, based on 73 article reviews
    e coli bacteriophage qβ - by Bioz Stars, 2026-02
    93/100 stars

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    Morphology of <t>Qβ</t> and recombinant phage derivatives. Panel 1: Phage plaques on the lawn of E. coli Q13. (P1) Wild <t>type</t> <t>Qβ;</t> (P2) QβF1; (P3) QβF2; (P4) QβF3; (P5) QβF4; and (P6) QβF5. All of the recombinant phages conserved their infectivity by inducing E. coli Q13 lysis (formation of clear zones or plaques). A mixture of plaques of different sizes was also found in the plates containing the recombinant phages compared to the wild type. Panel 2: Negative stain electron microgram of phages. (A) Wild type Qβ; (B) QβF1; (C) QβF2; (D) QβF3; (E) QβF4; and (F) QβF5. Nickeled gold of 10 nm (black dots) was used for detection. The scale bars on the micrographs are 50 nm. The size of the recombinant phages was almost identical to the wild type.
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    Morphology of <t>Qβ</t> and recombinant phage derivatives. Panel 1: Phage plaques on the lawn of E. coli Q13. (P1) Wild <t>type</t> <t>Qβ;</t> (P2) QβF1; (P3) QβF2; (P4) QβF3; (P5) QβF4; and (P6) QβF5. All of the recombinant phages conserved their infectivity by inducing E. coli Q13 lysis (formation of clear zones or plaques). A mixture of plaques of different sizes was also found in the plates containing the recombinant phages compared to the wild type. Panel 2: Negative stain electron microgram of phages. (A) Wild type Qβ; (B) QβF1; (C) QβF2; (D) QβF3; (E) QβF4; and (F) QβF5. Nickeled gold of 10 nm (black dots) was used for detection. The scale bars on the micrographs are 50 nm. The size of the recombinant phages was almost identical to the wild type.
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    Morphology of <t>Qβ</t> and recombinant phage derivatives. Panel 1: Phage plaques on the lawn of E. coli Q13. (P1) Wild <t>type</t> <t>Qβ;</t> (P2) QβF1; (P3) QβF2; (P4) QβF3; (P5) QβF4; and (P6) QβF5. All of the recombinant phages conserved their infectivity by inducing E. coli Q13 lysis (formation of clear zones or plaques). A mixture of plaques of different sizes was also found in the plates containing the recombinant phages compared to the wild type. Panel 2: Negative stain electron microgram of phages. (A) Wild type Qβ; (B) QβF1; (C) QβF2; (D) QβF3; (E) QβF4; and (F) QβF5. Nickeled gold of 10 nm (black dots) was used for detection. The scale bars on the micrographs are 50 nm. The size of the recombinant phages was almost identical to the wild type.
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    ATCC l pneumophila atcc 33 152 p aeruginosa atcc 10 145 v parahaemolyticus nbrc 12 711 e coli ifo 3301 b subtilis atcc 6633 f calicivirus atcc vr 782 qbeta atcc 23 631 b1 ms2 atcc
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    Summary of UV based inactivation studies.
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    Morphology of Qβ and recombinant phage derivatives. Panel 1: Phage plaques on the lawn of E. coli Q13. (P1) Wild type Qβ; (P2) QβF1; (P3) QβF2; (P4) QβF3; (P5) QβF4; and (P6) QβF5. All of the recombinant phages conserved their infectivity by inducing E. coli Q13 lysis (formation of clear zones or plaques). A mixture of plaques of different sizes was also found in the plates containing the recombinant phages compared to the wild type. Panel 2: Negative stain electron microgram of phages. (A) Wild type Qβ; (B) QβF1; (C) QβF2; (D) QβF3; (E) QβF4; and (F) QβF5. Nickeled gold of 10 nm (black dots) was used for detection. The scale bars on the micrographs are 50 nm. The size of the recombinant phages was almost identical to the wild type.

    Journal: ACS Omega

    Article Title: Mapping Immunological, Host Receptor Binding Determinants, and Cathepsin Cleavage Site of EBOV Glycoprotein Utilizing the Qubevirus Platform

    doi: 10.1021/acsomega.5c00408

    Figure Lengend Snippet: Morphology of Qβ and recombinant phage derivatives. Panel 1: Phage plaques on the lawn of E. coli Q13. (P1) Wild type Qβ; (P2) QβF1; (P3) QβF2; (P4) QβF3; (P5) QβF4; and (P6) QβF5. All of the recombinant phages conserved their infectivity by inducing E. coli Q13 lysis (formation of clear zones or plaques). A mixture of plaques of different sizes was also found in the plates containing the recombinant phages compared to the wild type. Panel 2: Negative stain electron microgram of phages. (A) Wild type Qβ; (B) QβF1; (C) QβF2; (D) QβF3; (E) QβF4; and (F) QβF5. Nickeled gold of 10 nm (black dots) was used for detection. The scale bars on the micrographs are 50 nm. The size of the recombinant phages was almost identical to the wild type.

    Article Snippet: The wild type Qβ phage was obtained from ATCC (American Type Culture Collection) number: 23631-B1.

    Techniques: Recombinant, Infection, Lysis, Staining

    Binding activity of Ebola glycoprotein identified on the RNA Qβ phage platform to anti-EBOV GP antibody. (A) Recombinant phages QβF1, QβF2, QβF3, and QβF4 were subjected to immunoblotting assay (dot blot) with anti-EBOV GP antibody in comparison with the wild type Qβ (WT). (B) Quantitative ELISA of the anti-EBOV GP antibody with the immunogenic fractions on Qβ phage.

    Journal: ACS Omega

    Article Title: Mapping Immunological, Host Receptor Binding Determinants, and Cathepsin Cleavage Site of EBOV Glycoprotein Utilizing the Qubevirus Platform

    doi: 10.1021/acsomega.5c00408

    Figure Lengend Snippet: Binding activity of Ebola glycoprotein identified on the RNA Qβ phage platform to anti-EBOV GP antibody. (A) Recombinant phages QβF1, QβF2, QβF3, and QβF4 were subjected to immunoblotting assay (dot blot) with anti-EBOV GP antibody in comparison with the wild type Qβ (WT). (B) Quantitative ELISA of the anti-EBOV GP antibody with the immunogenic fractions on Qβ phage.

    Article Snippet: The wild type Qβ phage was obtained from ATCC (American Type Culture Collection) number: 23631-B1.

    Techniques: Binding Assay, Activity Assay, Recombinant, Western Blot, Dot Blot, Comparison, Enzyme-linked Immunosorbent Assay

    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:

    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 , 265 280 300 , L. pneumophila ATCC 33,152 P. aeruginosa ATCC 10,145 V. parahaemolyticus NBRC 12,711 E. coli IFO 3301 B. subtilis ATCC 6633 F. calicivirus ATCC VR-782 QBeta ATCC 23,631 B1 MS2 ATCC 15,597 B1 , ( ) .

    Techniques: