ccl 34  (ATCC)


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    ATCC ccl 34
    Ccl 34, 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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    madin darby canine kidney mdck ccl 34 cells  (ATCC)


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    ATCC madin darby canine kidney mdck ccl 34 cells
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    cell lines madin darby canine kidney mdck cells atcc ccl 34 oligonucleotides primers  (ATCC)


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    ATCC cell lines madin darby canine kidney mdck cells atcc ccl 34 oligonucleotides primers
    Cell Lines Madin Darby Canine Kidney Mdck Cells Atcc Ccl 34 Oligonucleotides Primers, 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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    mdck cells ccl 34  (ATCC)


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    ATCC mdck cells ccl 34
    a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK <t>CCL-34</t> cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.
    Mdck Cells Ccl 34, 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 "Neu5Gc binding loss of subtype H7 influenza A virus facilitates adaptation to gallinaceous poultry following transmission from waterbirds but restricts spillback"

    Article Title: Neu5Gc binding loss of subtype H7 influenza A virus facilitates adaptation to gallinaceous poultry following transmission from waterbirds but restricts spillback

    Journal: bioRxiv

    doi: 10.1101/2024.01.02.573990

    a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK CCL-34 cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.
    Figure Legend Snippet: a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK CCL-34 cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.

    Techniques Used: Generated, Infection

    mdck ccl 34 cells  (ATCC)


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    ATCC mdck ccl 34 cells
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    ccl 34 software  (ATCC)


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    ATCC ccl 34 software
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    mdck cells ccl 34  (ATCC)


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    ATCC mdck cells ccl 34
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    ccl 34  (ATCC)


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    ATCC ccl 34
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    ccl 34  (ATCC)


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    ATCC ccl 34
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    ccl 34  (ATCC)


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    ATCC ccl 34
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    ATCC ccl 34
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    ATCC cell lines madin darby canine kidney mdck cells atcc ccl 34 oligonucleotides primers
    Cell Lines Madin Darby Canine Kidney Mdck Cells Atcc Ccl 34 Oligonucleotides Primers, 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 mdck cells ccl 34
    a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK <t>CCL-34</t> cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.
    Mdck Cells Ccl 34, 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 mdck ccl 34 cells
    a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK <t>CCL-34</t> cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.
    Mdck Ccl 34 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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    ATCC ccl 34 software
    a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK <t>CCL-34</t> cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.
    Ccl 34 Software, 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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    a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK CCL-34 cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.

    Journal: bioRxiv

    Article Title: Neu5Gc binding loss of subtype H7 influenza A virus facilitates adaptation to gallinaceous poultry following transmission from waterbirds but restricts spillback

    doi: 10.1101/2024.01.02.573990

    Figure Lengend Snippet: a) Growth kinetics of H7 influenza A viruses and mutants in MDCK-wt and MDCK-Gc cells. All viruses had HA genes from H7 viruses and the other seven from PR8, and three mutants were generated using the HA gene of Ck/WX13 as a template. Supernatants were collected at 12-, 24-, 48-, and 72-hours post-infection (hpi) and titrated by TCID50 in MDCK CCL-34 cells. Two-way repeated measures ANOVA were used to compare time-course growth data of H7 viruses among different cells. Statistical comparisons were shown as follows: not significantly different as n.s. (P > 0.05); P ≤ 0.05 as *; P < 0.01 as **; P < 0.001 as ***; and P < 0.0001 as ****. (b) HA amino acid polymorphisms detected in the seed viruses and the viruses from the 5th passage in MDCK-wt and MDCK-Gc cells. The viruses rgCk/WX13 and rgMall/NJ10, which have an HA gene from rgCk/WX13 and rgMall/NJ10, respectively, and other seven genes from PR8 were passaged five times in MDCK-wt and MDCK-Gc cells. The two most abundant nonsynonymous mutations in the HA protein were plotted to visualize adaptive amino acid substitutions caused by cell passages. The location of the RBS in the HA protein was marked green.

    Article Snippet: The MDCK cells (CCL-34) were obtained from American Type Culture Collection (ATCC).

    Techniques: Generated, Infection