e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), <t>E.</t> <t>coli</t> <t>BL21</t> <t>(DE3)</t> ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection"

    Article Title: Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection

    Journal: Journal of Nanobiotechnology

    doi: 10.1186/s12951-024-02553-x

    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    Figure Legend Snippet: Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant

    Techniques Used: Membrane, Generated, SDS Page

    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), <t>E.</t> <t>coli</t> <t>BL21</t> <t>(DE3)</t> ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection"

    Article Title: Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection

    Journal: Journal of Nanobiotechnology

    doi: 10.1186/s12951-024-02553-x

    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    Figure Legend Snippet: Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant

    Techniques Used: Membrane, Generated, SDS Page

    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), <t>E.</t> <t>coli</t> <t>BL21</t> <t>(DE3)</t> ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 86 stars, based on 1 article reviews
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    e coli bl21 de3 - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection"

    Article Title: Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection

    Journal: Journal of Nanobiotechnology

    doi: 10.1186/s12951-024-02553-x

    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    Figure Legend Snippet: Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant

    Techniques Used: Membrane, Generated, SDS Page

    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), <t>E.</t> <t>coli</t> <t>BL21</t> <t>(DE3)</t> ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/e coli bl21 de3/product/ATCC
    Average 86 stars, based on 1 article reviews
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    Images

    1) Product Images from "Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection"

    Article Title: Outer membrane vesicles generated by an exogenous bacteriophage lysin and protection against Acinetobacter baumannii infection

    Journal: Journal of Nanobiotechnology

    doi: 10.1186/s12951-024-02553-x

    Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant
    Figure Legend Snippet: Outer membrane vesicles generated natively (nOMVs) and by LysP53 (LOMVs). A – F TEM images of nOMVs and LOMVs from A. baumannii WHG40137 ( A and D ), E. coli BL21 (DE3) ( B and E ), and S. Enteritidis ATCC 13076 ( C and F ); G – I SDS-PAGE analysis of protein compositions of nOMVs and LOMVs from A. baumannii WHG40137 ( G ), E. coli BL21 (DE3) ( H ) and S. Enteritidis ATCC 13076 ( I ); J Protein yields of nOMVs and LOMVs. **P < 0.01, ****P < 0.0001, and ns not significant

    Techniques Used: Membrane, Generated, SDS Page

    e coli strain bl21 de3  (ATCC)


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    ATCC e coli strain bl21 de3
    E Coli Strain Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    e coli bl21 de3 codonplus ril competent cells  (ATCC)


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    ATCC e coli bl21 de3 codonplus ril competent cells
    E Coli Bl21 De3 Codonplus Ril Competent Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    e coli bl21 de3  (ATCC)


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    ATCC e coli bl21 de3
    Post-translational modifications required for the production of holo-c-type cytochromes (Cytc) in <t>E.</t> <t>coli</t> – . Transcription and translation of the Cytc encoding gene and mRNA take place in the cytoplasm while co-factor integration and folding occur in the periplasm. The signal peptide of the apo-protein leads to translocation into the periplasm via the general secretory (Sec) translocation pathway . Heme is synthesized in the cytoplasm from δ-aminolevulinic acid (δ-ALA), transported into the periplasm and delivered to the apo-Cytc via CcmC, CcmE, and CcmF. CcmF catalyzes the covalent attachment of heme to the cysteine residues of the Cytc binding motif. CcmA and CcmB are predicted to be transporter proteins. However, it is unclear what substrate they transport. CcmD stabilizes CcmE in the membrane. Electrons required for the formation of the thioether bonds are delivered to the apo-Cytc via CcmH, CcmG, and DsbD. After integration of heme c and folding, holo-Cytc remains soluble in the periplasm or is integrated into a membrane.
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Vibrio natriegens as a superior host for the production of c-type cytochromes and difficult-to-express redox proteins"

    Article Title: Vibrio natriegens as a superior host for the production of c-type cytochromes and difficult-to-express redox proteins

    Journal: Scientific Reports

    doi: 10.1038/s41598-024-54097-7

    Post-translational modifications required for the production of holo-c-type cytochromes (Cytc) in E. coli – . Transcription and translation of the Cytc encoding gene and mRNA take place in the cytoplasm while co-factor integration and folding occur in the periplasm. The signal peptide of the apo-protein leads to translocation into the periplasm via the general secretory (Sec) translocation pathway . Heme is synthesized in the cytoplasm from δ-aminolevulinic acid (δ-ALA), transported into the periplasm and delivered to the apo-Cytc via CcmC, CcmE, and CcmF. CcmF catalyzes the covalent attachment of heme to the cysteine residues of the Cytc binding motif. CcmA and CcmB are predicted to be transporter proteins. However, it is unclear what substrate they transport. CcmD stabilizes CcmE in the membrane. Electrons required for the formation of the thioether bonds are delivered to the apo-Cytc via CcmH, CcmG, and DsbD. After integration of heme c and folding, holo-Cytc remains soluble in the periplasm or is integrated into a membrane.
    Figure Legend Snippet: Post-translational modifications required for the production of holo-c-type cytochromes (Cytc) in E. coli – . Transcription and translation of the Cytc encoding gene and mRNA take place in the cytoplasm while co-factor integration and folding occur in the periplasm. The signal peptide of the apo-protein leads to translocation into the periplasm via the general secretory (Sec) translocation pathway . Heme is synthesized in the cytoplasm from δ-aminolevulinic acid (δ-ALA), transported into the periplasm and delivered to the apo-Cytc via CcmC, CcmE, and CcmF. CcmF catalyzes the covalent attachment of heme to the cysteine residues of the Cytc binding motif. CcmA and CcmB are predicted to be transporter proteins. However, it is unclear what substrate they transport. CcmD stabilizes CcmE in the membrane. Electrons required for the formation of the thioether bonds are delivered to the apo-Cytc via CcmH, CcmG, and DsbD. After integration of heme c and folding, holo-Cytc remains soluble in the periplasm or is integrated into a membrane.

    Techniques Used: Translocation Assay, Synthesized, Binding Assay, Membrane

    Comparison of the chromosomal ccm operon organization in V. natriegens and E. coli . The ccm genes (cytochrome c maturation; red) in V. natriegens form a separate operon on chromosome 1, while the nap genes (green), encoding a periplasmic nitrate reductase , are distributed across chromosome 2. Chromosomal promoter prediction revealed a potential promoter region upstream of ccmA . A RpoD16 binding site was predicted in this region, suggesting that the ccm genes are expressed during exponential aerobic growth. In E. coli the ccm genes are part of the aeg46.5 operon together with the nap genes. Expression of all genes in this operon is only activated under anaerobic conditions . A fumarate nitrate regulator (FNR) binding site was predicted in the promoter region upstream of napF .
    Figure Legend Snippet: Comparison of the chromosomal ccm operon organization in V. natriegens and E. coli . The ccm genes (cytochrome c maturation; red) in V. natriegens form a separate operon on chromosome 1, while the nap genes (green), encoding a periplasmic nitrate reductase , are distributed across chromosome 2. Chromosomal promoter prediction revealed a potential promoter region upstream of ccmA . A RpoD16 binding site was predicted in this region, suggesting that the ccm genes are expressed during exponential aerobic growth. In E. coli the ccm genes are part of the aeg46.5 operon together with the nap genes. Expression of all genes in this operon is only activated under anaerobic conditions . A fumarate nitrate regulator (FNR) binding site was predicted in the promoter region upstream of napF .

    Techniques Used: Comparison, Binding Assay, Expressing

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    ATCC e coli bl21 de3
    E Coli Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC e coli strain bl21 de3
    E Coli Strain Bl21 De3, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC e coli bl21 de3 codonplus ril competent cells
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