alexa fluor 488 conjugated goat anti mouse igg antibody Search Results


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  • 99
    Thermo Fisher alexa fluor 488 conjugated goat anti mouse igg
    Alexa Fluor 488 Conjugated Goat Anti Mouse Igg, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/alexa fluor 488 conjugated goat anti mouse igg/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    alexa fluor 488 conjugated goat anti mouse igg - by Bioz Stars, 2021-06
    99/100 stars
      Buy from Supplier

    99
    Thermo Fisher goat anti mouse igg h l cross adsorbed secondary antibody
    Goat Anti Mouse Igg H L Cross Adsorbed Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti mouse igg h l cross adsorbed secondary antibody/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    goat anti mouse igg h l cross adsorbed secondary antibody - by Bioz Stars, 2021-06
    99/100 stars
      Buy from Supplier

    86
    Thermo Fisher alexa fluor 488 conjugated goat anti mouse igg antibody
    Growth characteristics of rIBVs BeauR-M41(S1) and BeauR-M41(S2) P 3 -CK on CK and Vero cells. (A and B) Chick kidney cells (A) and Vero cells (B) in 6-well plates were infected with Beau-R, M41-CK, BeauR-M41(S), BeauR-M41(S1) P 3 -CK, and BeauR-M41(S2) P 3 -CK at an MOI of 0.5. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (C to H) Vero cells were mock infected (C) or were infected with Beau-R (D), M41-CK (E), BeauR-M41(S) (F), BeauR-M41(S1) P 3 -CK (G), or BeauR-M41(S2) P 3 -CK (H). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody <t>Alexa</t> Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.
    Alexa Fluor 488 Conjugated Goat Anti Mouse Igg Antibody, supplied by Thermo Fisher, 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/alexa fluor 488 conjugated goat anti mouse igg antibody/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    alexa fluor 488 conjugated goat anti mouse igg antibody - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

    99
    Thermo Fisher goat anti mouse igg h l highly cross adsorbed secondary antibody
    Growth characteristics of rIBVs BeauR-M41(S1) and BeauR-M41(S2) P 3 -CK on CK and Vero cells. (A and B) Chick kidney cells (A) and Vero cells (B) in 6-well plates were infected with Beau-R, M41-CK, BeauR-M41(S), BeauR-M41(S1) P 3 -CK, and BeauR-M41(S2) P 3 -CK at an MOI of 0.5. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (C to H) Vero cells were mock infected (C) or were infected with Beau-R (D), M41-CK (E), BeauR-M41(S) (F), BeauR-M41(S1) P 3 -CK (G), or BeauR-M41(S2) P 3 -CK (H). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody <t>Alexa</t> Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.
    Goat Anti Mouse Igg H L Highly Cross Adsorbed Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti mouse igg h l highly cross adsorbed secondary antibody/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    goat anti mouse igg h l highly cross adsorbed secondary antibody - by Bioz Stars, 2021-06
    99/100 stars
      Buy from Supplier

    N/A
    Secondary Host Note Goat Conjugation Note Alexa Fluor 488
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    Image Search Results


    Growth characteristics of rIBVs BeauR-M41(S1) and BeauR-M41(S2) P 3 -CK on CK and Vero cells. (A and B) Chick kidney cells (A) and Vero cells (B) in 6-well plates were infected with Beau-R, M41-CK, BeauR-M41(S), BeauR-M41(S1) P 3 -CK, and BeauR-M41(S2) P 3 -CK at an MOI of 0.5. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (C to H) Vero cells were mock infected (C) or were infected with Beau-R (D), M41-CK (E), BeauR-M41(S) (F), BeauR-M41(S1) P 3 -CK (G), or BeauR-M41(S2) P 3 -CK (H). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.

    Journal: Journal of Virology

    Article Title: The S2 Subunit of Infectious Bronchitis Virus Beaudette Is a Determinant of Cellular Tropism

    doi: 10.1128/JVI.01044-18

    Figure Lengend Snippet: Growth characteristics of rIBVs BeauR-M41(S1) and BeauR-M41(S2) P 3 -CK on CK and Vero cells. (A and B) Chick kidney cells (A) and Vero cells (B) in 6-well plates were infected with Beau-R, M41-CK, BeauR-M41(S), BeauR-M41(S1) P 3 -CK, and BeauR-M41(S2) P 3 -CK at an MOI of 0.5. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (C to H) Vero cells were mock infected (C) or were infected with Beau-R (D), M41-CK (E), BeauR-M41(S) (F), BeauR-M41(S1) P 3 -CK (G), or BeauR-M41(S2) P 3 -CK (H). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.

    Article Snippet: IBV-infected cells were identified by incubation with a 1:400 dilution of mouse anti-double-stranded RNA (anti-dsRNA) J2 IgG2a monoclonal antibody (English and Scientific Consulting Bt.) and detected with Alexa Fluor 488-conjugated goat anti-mouse IgG antibody (Invitrogen) diluted 1:200.

    Techniques: Infection, Immunolabeling, Labeling

    Growth characteristics of rIBVs BeauR-S-MM and BeauR-M41-S-BSM P 3 -CK on CK and Vero cells. (A and D) Chick kidney cells (A) and Vero cells (D) in 6-well plates were infected with Beau-R, M41-CK, BeauR-M41(S), BeauR-S-MM P 3 -CK, and BeauR-M41-S-BSM P 3 -CK at an MOI of 0.5. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (B and C) Vero cells were infected with BeauR-M41-S-BSM P 3 -CK (B) and BeauR-S-MM P 3 -CK (C). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.

    Journal: Journal of Virology

    Article Title: The S2 Subunit of Infectious Bronchitis Virus Beaudette Is a Determinant of Cellular Tropism

    doi: 10.1128/JVI.01044-18

    Figure Lengend Snippet: Growth characteristics of rIBVs BeauR-S-MM and BeauR-M41-S-BSM P 3 -CK on CK and Vero cells. (A and D) Chick kidney cells (A) and Vero cells (D) in 6-well plates were infected with Beau-R, M41-CK, BeauR-M41(S), BeauR-S-MM P 3 -CK, and BeauR-M41-S-BSM P 3 -CK at an MOI of 0.5. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (B and C) Vero cells were infected with BeauR-M41-S-BSM P 3 -CK (B) and BeauR-S-MM P 3 -CK (C). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.

    Article Snippet: IBV-infected cells were identified by incubation with a 1:400 dilution of mouse anti-double-stranded RNA (anti-dsRNA) J2 IgG2a monoclonal antibody (English and Scientific Consulting Bt.) and detected with Alexa Fluor 488-conjugated goat anti-mouse IgG antibody (Invitrogen) diluted 1:200.

    Techniques: Infection, Immunolabeling, Labeling

    Growth characteristics of rIBVs with modified S2 subunits on CK and Vero cells. (A and B) Chick kidney cells (A) and Vero cells (B) in 6-well plates were infected with Beau-R, BeauR-M41(S), BeauR-M41-S-BSM P 3 -CK, BeauR-M41-S-BSM-N 617 S P 3 -CK, BeauR-M41-S-BSM-L 578 F-N 617 S P 3 -CK, BeauR-M41-S-BSM-I 1000 V P 3 -CK, BeauR-M41-S-BSM-L 857 F-I 1000 V P 3 -CK, BeauR-M41-S-BSM-N 826 S-L 857 F-I 1000 V P 3 -CK, and BeauR-M41-S-BSM-L 578 F-N 617 S-N 826 S-L 857 F-I 1000 V P 3 -CK at an MOI of 0.05. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (C to H) Vero cells were infected with BeauR-M41-S-BSM-N 617 S P 3 -CK (C), BeauR-M41-S-BSM-L 578 F-N 617 S P 3 -CK (D), BeauR-M41-S-BSM-I 1000 V P 3 -CK (E), BeauR-M41-S-BSM-N 826 S-L 857 F-I 1000 V P 3 -CK (F), BeauR-M41-S-BSM-N 826 S-L 857 F-I 1000 V P 3 -CK (G), and BeauR-M41-S-BSM-L 578 F-N 617 S-N 826 S-L 857 F-I 1000 V P 3 -CK (H). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.

    Journal: Journal of Virology

    Article Title: The S2 Subunit of Infectious Bronchitis Virus Beaudette Is a Determinant of Cellular Tropism

    doi: 10.1128/JVI.01044-18

    Figure Lengend Snippet: Growth characteristics of rIBVs with modified S2 subunits on CK and Vero cells. (A and B) Chick kidney cells (A) and Vero cells (B) in 6-well plates were infected with Beau-R, BeauR-M41(S), BeauR-M41-S-BSM P 3 -CK, BeauR-M41-S-BSM-N 617 S P 3 -CK, BeauR-M41-S-BSM-L 578 F-N 617 S P 3 -CK, BeauR-M41-S-BSM-I 1000 V P 3 -CK, BeauR-M41-S-BSM-L 857 F-I 1000 V P 3 -CK, BeauR-M41-S-BSM-N 826 S-L 857 F-I 1000 V P 3 -CK, and BeauR-M41-S-BSM-L 578 F-N 617 S-N 826 S-L 857 F-I 1000 V P 3 -CK at an MOI of 0.05. The supernatant was harvested at 1, 12, 24, 48, and 72 h postinfection and titrated on CK cells. Three replicates were performed, and the averages were taken. Error bars indicate the standard error of the mean. (C to H) Vero cells were infected with BeauR-M41-S-BSM-N 617 S P 3 -CK (C), BeauR-M41-S-BSM-L 578 F-N 617 S P 3 -CK (D), BeauR-M41-S-BSM-I 1000 V P 3 -CK (E), BeauR-M41-S-BSM-N 826 S-L 857 F-I 1000 V P 3 -CK (F), BeauR-M41-S-BSM-N 826 S-L 857 F-I 1000 V P 3 -CK (G), and BeauR-M41-S-BSM-L 578 F-N 617 S-N 826 S-L 857 F-I 1000 V P 3 -CK (H). Infected cells were fixed at 24 h postinfection and immunolabeled with mouse anti-dsRNA and secondary antibody Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (green; Invitrogen). Nuclei were labeled with DAPI (blue). Bars, 50 μm.

    Article Snippet: IBV-infected cells were identified by incubation with a 1:400 dilution of mouse anti-double-stranded RNA (anti-dsRNA) J2 IgG2a monoclonal antibody (English and Scientific Consulting Bt.) and detected with Alexa Fluor 488-conjugated goat anti-mouse IgG antibody (Invitrogen) diluted 1:200.

    Techniques: Modification, Infection, Immunolabeling, Labeling