alexa fluor 568-conjugated goat anti-rabbit igg antibody Search Results


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  • 99
    Thermo Fisher alexa fluor 568 conjugated goat anti rabbit igg secondary antibody
    Alexa Fluor 568 Conjugated Goat Anti Rabbit Igg Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/alexa fluor 568 conjugated goat anti rabbit igg secondary antibody/product/Thermo Fisher
    Average 99 stars, based on 20 article reviews
    Price from $9.99 to $1999.99
    alexa fluor 568 conjugated goat anti rabbit igg secondary antibody - by Bioz Stars, 2020-05
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    88
    Thermo Fisher alexa fluor 568 conjugated goat anti rabbit igg antibody
    Adherence and invasion of A. baumannii ATCC19606 T and isogenic AbOmpA - mutant in epithelial cells . (A). Adherence of A. baumannii to epithelial cells. NCI-H292 cells were infected with A. baumannii strains at an MOI of 100 for 1 h. Actin was stained with <t>Alexa</t> Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). (B). NCI-H292 and HEp-2 cells were infected with A. baumannii at an MOI of 100 for 5 h. Invasion efficiency was expressed as the number of bacteria per well using the gentamicin protection assay. Results represent the mean and standard deviation of three separate experiments on separately days. * P
    Alexa Fluor 568 Conjugated Goat Anti Rabbit Igg Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 193 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/alexa fluor 568 conjugated goat anti rabbit igg antibody/product/Thermo Fisher
    Average 88 stars, based on 193 article reviews
    Price from $9.99 to $1999.99
    alexa fluor 568 conjugated goat anti rabbit igg antibody - by Bioz Stars, 2020-05
    88/100 stars
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    96
    Abcam goat anti rabbit 568 conjugated secondary antibody
    Adherence and invasion of A. baumannii ATCC19606 T and isogenic AbOmpA - mutant in epithelial cells . (A). Adherence of A. baumannii to epithelial cells. NCI-H292 cells were infected with A. baumannii strains at an MOI of 100 for 1 h. Actin was stained with <t>Alexa</t> Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). (B). NCI-H292 and HEp-2 cells were infected with A. baumannii at an MOI of 100 for 5 h. Invasion efficiency was expressed as the number of bacteria per well using the gentamicin protection assay. Results represent the mean and standard deviation of three separate experiments on separately days. * P
    Goat Anti Rabbit 568 Conjugated Secondary Antibody, supplied by Abcam, used in various techniques. Bioz Stars score: 96/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti rabbit 568 conjugated secondary antibody/product/Abcam
    Average 96 stars, based on 7 article reviews
    Price from $9.99 to $1999.99
    goat anti rabbit 568 conjugated secondary antibody - by Bioz Stars, 2020-05
    96/100 stars
      Buy from Supplier

    99
    Thermo Fisher goat anti rabbit igg secondary antibody conjugated to alexa fluor 568
    Adherence and invasion of A. baumannii ATCC19606 T and isogenic AbOmpA - mutant in epithelial cells . (A). Adherence of A. baumannii to epithelial cells. NCI-H292 cells were infected with A. baumannii strains at an MOI of 100 for 1 h. Actin was stained with <t>Alexa</t> Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). (B). NCI-H292 and HEp-2 cells were infected with A. baumannii at an MOI of 100 for 5 h. Invasion efficiency was expressed as the number of bacteria per well using the gentamicin protection assay. Results represent the mean and standard deviation of three separate experiments on separately days. * P
    Goat Anti Rabbit Igg Secondary Antibody Conjugated To Alexa Fluor 568, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti rabbit igg secondary antibody conjugated to alexa fluor 568/product/Thermo Fisher
    Average 99 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    goat anti rabbit igg secondary antibody conjugated to alexa fluor 568 - by Bioz Stars, 2020-05
    99/100 stars
      Buy from Supplier

    91
    Millipore alexa fluor 568 conjugated goat anti rabbit igg
    Adherence and invasion of A. baumannii ATCC19606 T and isogenic AbOmpA - mutant in epithelial cells . (A). Adherence of A. baumannii to epithelial cells. NCI-H292 cells were infected with A. baumannii strains at an MOI of 100 for 1 h. Actin was stained with <t>Alexa</t> Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). (B). NCI-H292 and HEp-2 cells were infected with A. baumannii at an MOI of 100 for 5 h. Invasion efficiency was expressed as the number of bacteria per well using the gentamicin protection assay. Results represent the mean and standard deviation of three separate experiments on separately days. * P
    Alexa Fluor 568 Conjugated Goat Anti Rabbit Igg, supplied by Millipore, used in various techniques. Bioz Stars score: 91/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/alexa fluor 568 conjugated goat anti rabbit igg/product/Millipore
    Average 91 stars, based on 7 article reviews
    Price from $9.99 to $1999.99
    alexa fluor 568 conjugated goat anti rabbit igg - by Bioz Stars, 2020-05
    91/100 stars
      Buy from Supplier

    90
    Thermo Fisher goat anti rabbit igg alexa fluor 568 conjugate
    Validation of UQCRC1 expression by immunofluorescence staining. Frozen sections from stage I and III GC ( A ) and their adjacent normal gastric tissues ( B ) were incubated with antibody against human UQCRC1, followed by goat anti-rabbit <t>IgG–Alexa</t> Fluor® 568 conjugate. Nuclei are stained with DAPI (blue).
    Goat Anti Rabbit Igg Alexa Fluor 568 Conjugate, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti rabbit igg alexa fluor 568 conjugate/product/Thermo Fisher
    Average 90 stars, based on 11 article reviews
    Price from $9.99 to $1999.99
    goat anti rabbit igg alexa fluor 568 conjugate - by Bioz Stars, 2020-05
    90/100 stars
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    Image Search Results


    Adherence and invasion of A. baumannii ATCC19606 T and isogenic AbOmpA - mutant in epithelial cells . (A). Adherence of A. baumannii to epithelial cells. NCI-H292 cells were infected with A. baumannii strains at an MOI of 100 for 1 h. Actin was stained with Alexa Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). (B). NCI-H292 and HEp-2 cells were infected with A. baumannii at an MOI of 100 for 5 h. Invasion efficiency was expressed as the number of bacteria per well using the gentamicin protection assay. Results represent the mean and standard deviation of three separate experiments on separately days. * P

    Journal: BMC Microbiology

    Article Title: Acinetobacter baumannii invades epithelial cells and outer membrane protein A mediates interactions with epithelial cells

    doi: 10.1186/1471-2180-8-216

    Figure Lengend Snippet: Adherence and invasion of A. baumannii ATCC19606 T and isogenic AbOmpA - mutant in epithelial cells . (A). Adherence of A. baumannii to epithelial cells. NCI-H292 cells were infected with A. baumannii strains at an MOI of 100 for 1 h. Actin was stained with Alexa Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). (B). NCI-H292 and HEp-2 cells were infected with A. baumannii at an MOI of 100 for 5 h. Invasion efficiency was expressed as the number of bacteria per well using the gentamicin protection assay. Results represent the mean and standard deviation of three separate experiments on separately days. * P

    Article Snippet: A. baumannii was labeled with polyclonal anti-rabbit AbOmpA antibody (1:1,000), followed by Alexa Fluor® 568-conjugated goat anti-rabbit IgG antibody (Molecular Probes).

    Techniques: Mutagenesis, Infection, Staining, Standard Deviation

    Invasion of A. baumannii in epithelial cells . (A) NCI-H292 cells were infected with A. baumannii ATCC 19606 T at an MOI of 100 up to 7 h. The colony-forming units were enumerated to measure the time-course of invasion. The result represents the mean ± standard deviation in duplicate wells and repeated a minimum of three separate times on separate days. (B) NCI-H292, HEp-2, and HeLa cells were infected with A. baumannii strains at an MOI of 100 for 5 h. (C) NCI-H292 cells were infected with A. baumannii 05KA103 at an MOI of 100 for 5 h. Actin was stained with Alexa Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). The analytical sectioning was performed from the top to the bottom of the cells. The figure represents a single section of the cells. (D). NCI-H292 cells were infected with A. baumannii ATCC 19606 T at an MOI of 100 for 5 h. Actin filaments have wrap-around-bacteria (white arrow). Red arrow indicates the extracellular bacteria. The figure represents all projection of sections in one picture.

    Journal: BMC Microbiology

    Article Title: Acinetobacter baumannii invades epithelial cells and outer membrane protein A mediates interactions with epithelial cells

    doi: 10.1186/1471-2180-8-216

    Figure Lengend Snippet: Invasion of A. baumannii in epithelial cells . (A) NCI-H292 cells were infected with A. baumannii ATCC 19606 T at an MOI of 100 up to 7 h. The colony-forming units were enumerated to measure the time-course of invasion. The result represents the mean ± standard deviation in duplicate wells and repeated a minimum of three separate times on separate days. (B) NCI-H292, HEp-2, and HeLa cells were infected with A. baumannii strains at an MOI of 100 for 5 h. (C) NCI-H292 cells were infected with A. baumannii 05KA103 at an MOI of 100 for 5 h. Actin was stained with Alexa Fluor ® 488 phalloidin (green). Bacteria were stained with polyclonal anti-rabbit AbOmpA antibody, followed by a secondary antibody Alexa Fluor ® 568 (red). The analytical sectioning was performed from the top to the bottom of the cells. The figure represents a single section of the cells. (D). NCI-H292 cells were infected with A. baumannii ATCC 19606 T at an MOI of 100 for 5 h. Actin filaments have wrap-around-bacteria (white arrow). Red arrow indicates the extracellular bacteria. The figure represents all projection of sections in one picture.

    Article Snippet: A. baumannii was labeled with polyclonal anti-rabbit AbOmpA antibody (1:1,000), followed by Alexa Fluor® 568-conjugated goat anti-rabbit IgG antibody (Molecular Probes).

    Techniques: Infection, Standard Deviation, Staining

    Flow cytometry of transfected cells stained separately for the ORF2 or ORF3 protein. HepG2/C3A and LLC-PK cells electroporated with transcripts from P6 (A), Sar55 (B), or Sar/S17 (C, D) were plated in 6 wells of a 6-well culture plate, incubated at 34.5°C, and harvested 7 (A, B) or 5 (C, D) days later. Cells in triplicate wells were stained for the ORF2 protein, followed by goat anti-human IgG labeled with Alexa Fluor 488 (open bars); cells in the other 3 wells were stained for the ORF3 protein, followed by goat anti-rabbit IgG also labeled with Alexa Fluor 488 (hatched bars). Flow cytometry was performed with the same settings for all samples. (A to C) Mean percentage of positive cells, in triplicate; (D) mean of the geometric mean fluorescence intensity in the same triplicate samples assayed for panel C. Shaded bars, ORF2; dotted bars, ORF3. Error bars indicate standard deviations. P values were determined by Student's t test; P values of less than 0.05 were statistically significant.

    Journal: Journal of Virology

    Article Title: Hepatitis E Virus Genotype 1 Infection of Swine Kidney Cells In Vitro Is Inhibited at Multiple Levels

    doi: 10.1128/JVI.02205-13

    Figure Lengend Snippet: Flow cytometry of transfected cells stained separately for the ORF2 or ORF3 protein. HepG2/C3A and LLC-PK cells electroporated with transcripts from P6 (A), Sar55 (B), or Sar/S17 (C, D) were plated in 6 wells of a 6-well culture plate, incubated at 34.5°C, and harvested 7 (A, B) or 5 (C, D) days later. Cells in triplicate wells were stained for the ORF2 protein, followed by goat anti-human IgG labeled with Alexa Fluor 488 (open bars); cells in the other 3 wells were stained for the ORF3 protein, followed by goat anti-rabbit IgG also labeled with Alexa Fluor 488 (hatched bars). Flow cytometry was performed with the same settings for all samples. (A to C) Mean percentage of positive cells, in triplicate; (D) mean of the geometric mean fluorescence intensity in the same triplicate samples assayed for panel C. Shaded bars, ORF2; dotted bars, ORF3. Error bars indicate standard deviations. P values were determined by Student's t test; P values of less than 0.05 were statistically significant.

    Article Snippet: Secondary antibodies were a mixture of Alexa Fluor 488-conjugated goat anti-human IgG (Molecular Probes) and Alexa Fluor 568-conjugated goat anti-rabbit IgG (Molecular Probes).

    Techniques: Flow Cytometry, Cytometry, Transfection, Staining, Incubation, Labeling, Fluorescence

    AFM immunocytochemistry identifying anti-opsin antibody binding ( A , B ). The anti-opsin antibody was used to evaluate whether AFM visualized the antibody binding because opsin is the major constituent protein that localizes to ROS. A: Immunofluorescence images of ROS labelled with the anti-opsin antibody and the secondary antibody conjugated to Alexa 568. The inset shows an enlargement of the white box. ( B ) Correlative AFM images of the green boxed area in A. Compared with the control ( C ), the anti-opsin antibodies conjugated with the secondary antibodies appear to have a complicated shape and bind heavily to disks in the ROS. The disk arrangement is also apparent behind the labelling at higher magnifications (inset). ( C ) Control AFM image incubated with non-immune IgG.

    Journal: Scientific Reports

    Article Title: A Cryosectioning Technique for the Observation of Intracellular Structures and Immunocytochemistry of Tissues in Atomic Force Microscopy (AFM)

    doi: 10.1038/s41598-017-06942-1

    Figure Lengend Snippet: AFM immunocytochemistry identifying anti-opsin antibody binding ( A , B ). The anti-opsin antibody was used to evaluate whether AFM visualized the antibody binding because opsin is the major constituent protein that localizes to ROS. A: Immunofluorescence images of ROS labelled with the anti-opsin antibody and the secondary antibody conjugated to Alexa 568. The inset shows an enlargement of the white box. ( B ) Correlative AFM images of the green boxed area in A. Compared with the control ( C ), the anti-opsin antibodies conjugated with the secondary antibodies appear to have a complicated shape and bind heavily to disks in the ROS. The disk arrangement is also apparent behind the labelling at higher magnifications (inset). ( C ) Control AFM image incubated with non-immune IgG.

    Article Snippet: Then the sections were incubated with goat anti-rabbit IgG conjugated to Alexa Fluor ® 568 (Invitrogen, Thermo Fisher Scientific, Inc.; Waltham, MA, USA) diluted 1:200 with PBS containing 1% BSA for 2 hr at room temperature.

    Techniques: Immunocytochemistry, Binding Assay, Immunofluorescence, Incubation

    Validation of UQCRC1 expression by immunofluorescence staining. Frozen sections from stage I and III GC ( A ) and their adjacent normal gastric tissues ( B ) were incubated with antibody against human UQCRC1, followed by goat anti-rabbit IgG–Alexa Fluor® 568 conjugate. Nuclei are stained with DAPI (blue).

    Journal: Scientific Reports

    Article Title: Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach

    doi: 10.1038/srep38871

    Figure Lengend Snippet: Validation of UQCRC1 expression by immunofluorescence staining. Frozen sections from stage I and III GC ( A ) and their adjacent normal gastric tissues ( B ) were incubated with antibody against human UQCRC1, followed by goat anti-rabbit IgG–Alexa Fluor® 568 conjugate. Nuclei are stained with DAPI (blue).

    Article Snippet: After washing, the sections were incubated with goat anti-rabbit IgG - Alexa Fluor® 568 conjugate (Thermo Fisher Scientific), or goat anti-mouse IgG- Alexa Fluor® 488 conjugate, followed by incubation with DAPI to stain nuclei.

    Techniques: Expressing, Immunofluorescence, Staining, Incubation

    Validation of Annexin A1 expression by immunofluorescence staining. Frozen sections from stage I and III GC ( A ) and their adjacent normal gastric tissues ( B ) were incubated with antibody against human Annexin A1, followed by goat anti-rabbit IgG - Alexa Fluor® 568 conjugate. Nuclei are stained with DAPI (blue).

    Journal: Scientific Reports

    Article Title: Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach

    doi: 10.1038/srep38871

    Figure Lengend Snippet: Validation of Annexin A1 expression by immunofluorescence staining. Frozen sections from stage I and III GC ( A ) and their adjacent normal gastric tissues ( B ) were incubated with antibody against human Annexin A1, followed by goat anti-rabbit IgG - Alexa Fluor® 568 conjugate. Nuclei are stained with DAPI (blue).

    Article Snippet: After washing, the sections were incubated with goat anti-rabbit IgG - Alexa Fluor® 568 conjugate (Thermo Fisher Scientific), or goat anti-mouse IgG- Alexa Fluor® 488 conjugate, followed by incubation with DAPI to stain nuclei.

    Techniques: Expressing, Immunofluorescence, Staining, Incubation