hrp labeled goat anti rabbit igg  (Boster Bio)


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    Boster Bio hrp labeled goat anti rabbit igg
    Detection of binding capability between selected phages amd EtMIC3-bc1 protein. EtMIC3-bc1-coated plate was incubated with thirty selected phages. The washed plate was then successively incubated with rabbit anti-M13 polyclonal antibody and horseradish peroxidase <t>(HRP)-conjugated</t> goat anti-rabbit <t>IgG.</t> Then substrate solution (0.01% H 2 O 2 and 1 mg/mL o-phenylenediamine) was added, and the reaction was stopped with 2 M sulfuric acid. The values of optical density (OD) at 490 nm was recorded. The blank control (BC), the negative control (NC) phages from G protein of porcine Vesicular Stomatitis Virus (VSV) (stored in our lab), and the positive control (PC) phages binding to EtAMA1 protein (stored in our lab) were used. Each sample was tested in triplicate. Values represent mean ± SD. Twenty-four selected phages clones showed higher binding capability than other clones (with the number of 1, 3, 13, 19, 23, 28), blank control and netative control phages ( P
    Hrp Labeled Goat Anti Rabbit Igg, supplied by Boster Bio, used in various techniques. Bioz Stars score: 97/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hrp labeled goat anti rabbit igg/product/Boster Bio
    Average 97 stars, based on 13 article reviews
    Price from $9.99 to $1999.99
    hrp labeled goat anti rabbit igg - by Bioz Stars, 2022-09
    97/100 stars

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    1) Product Images from "Specific EtMIC3-binding peptides inhibit Eimeria tenella sporozoites entry into host cells"

    Article Title: Specific EtMIC3-binding peptides inhibit Eimeria tenella sporozoites entry into host cells

    Journal: Veterinary Research

    doi: 10.1186/s13567-020-00873-y

    Detection of binding capability between selected phages amd EtMIC3-bc1 protein. EtMIC3-bc1-coated plate was incubated with thirty selected phages. The washed plate was then successively incubated with rabbit anti-M13 polyclonal antibody and horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG. Then substrate solution (0.01% H 2 O 2 and 1 mg/mL o-phenylenediamine) was added, and the reaction was stopped with 2 M sulfuric acid. The values of optical density (OD) at 490 nm was recorded. The blank control (BC), the negative control (NC) phages from G protein of porcine Vesicular Stomatitis Virus (VSV) (stored in our lab), and the positive control (PC) phages binding to EtAMA1 protein (stored in our lab) were used. Each sample was tested in triplicate. Values represent mean ± SD. Twenty-four selected phages clones showed higher binding capability than other clones (with the number of 1, 3, 13, 19, 23, 28), blank control and netative control phages ( P
    Figure Legend Snippet: Detection of binding capability between selected phages amd EtMIC3-bc1 protein. EtMIC3-bc1-coated plate was incubated with thirty selected phages. The washed plate was then successively incubated with rabbit anti-M13 polyclonal antibody and horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG. Then substrate solution (0.01% H 2 O 2 and 1 mg/mL o-phenylenediamine) was added, and the reaction was stopped with 2 M sulfuric acid. The values of optical density (OD) at 490 nm was recorded. The blank control (BC), the negative control (NC) phages from G protein of porcine Vesicular Stomatitis Virus (VSV) (stored in our lab), and the positive control (PC) phages binding to EtAMA1 protein (stored in our lab) were used. Each sample was tested in triplicate. Values represent mean ± SD. Twenty-four selected phages clones showed higher binding capability than other clones (with the number of 1, 3, 13, 19, 23, 28), blank control and netative control phages ( P

    Techniques Used: Binding Assay, Incubation, Negative Control, Positive Control, Clone Assay

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    Boster Bio hrp labeled goat anti rabbit igg
    Detection of binding capability between selected phages amd EtMIC3-bc1 protein. EtMIC3-bc1-coated plate was incubated with thirty selected phages. The washed plate was then successively incubated with rabbit anti-M13 polyclonal antibody and horseradish peroxidase <t>(HRP)-conjugated</t> goat anti-rabbit <t>IgG.</t> Then substrate solution (0.01% H 2 O 2 and 1 mg/mL o-phenylenediamine) was added, and the reaction was stopped with 2 M sulfuric acid. The values of optical density (OD) at 490 nm was recorded. The blank control (BC), the negative control (NC) phages from G protein of porcine Vesicular Stomatitis Virus (VSV) (stored in our lab), and the positive control (PC) phages binding to EtAMA1 protein (stored in our lab) were used. Each sample was tested in triplicate. Values represent mean ± SD. Twenty-four selected phages clones showed higher binding capability than other clones (with the number of 1, 3, 13, 19, 23, 28), blank control and netative control phages ( P
    Hrp Labeled Goat Anti Rabbit Igg, supplied by Boster Bio, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hrp labeled goat anti rabbit igg/product/Boster Bio
    Average 97 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hrp labeled goat anti rabbit igg - by Bioz Stars, 2022-09
    97/100 stars
      Buy from Supplier

    93
    Boster Bio horseradish peroxidase hrp labeled rabbit anti goat igg
    Western blot analysis of C3 and Bf in zebrafish egg cytosol (lane M: molecular marker; lane H: human serum; lane Z: zebrafish egg cytosol). The egg cytosol was electrophoresed on 12% SDS-PAGE gel using the buffer system of Laemmli. The proteins separated were blotted on nitrocellulose membrane and immunostained with rabbit anti-human C3 antibody or goat anti-human Bf antibody, followed by staining with <t>HRP-labeled</t> anti-rabbit <t>IgG</t> and HRP-labeled anti-goat IgG, respectively.
    Horseradish Peroxidase Hrp Labeled Rabbit Anti Goat Igg, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/horseradish peroxidase hrp labeled rabbit anti goat igg/product/Boster Bio
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    horseradish peroxidase hrp labeled rabbit anti goat igg - by Bioz Stars, 2022-09
    93/100 stars
      Buy from Supplier

    95
    Boster Bio hrp conjugated goat anti rabbit igg sabc kit
    Western blot analysis of C3 and Bf in zebrafish egg cytosol (lane M: molecular marker; lane H: human serum; lane Z: zebrafish egg cytosol). The egg cytosol was electrophoresed on 12% SDS-PAGE gel using the buffer system of Laemmli. The proteins separated were blotted on nitrocellulose membrane and immunostained with rabbit anti-human C3 antibody or goat anti-human Bf antibody, followed by staining with <t>HRP-labeled</t> anti-rabbit <t>IgG</t> and HRP-labeled anti-goat IgG, respectively.
    Hrp Conjugated Goat Anti Rabbit Igg Sabc Kit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hrp conjugated goat anti rabbit igg sabc kit/product/Boster Bio
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hrp conjugated goat anti rabbit igg sabc kit - by Bioz Stars, 2022-09
    95/100 stars
      Buy from Supplier

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    Detection of binding capability between selected phages amd EtMIC3-bc1 protein. EtMIC3-bc1-coated plate was incubated with thirty selected phages. The washed plate was then successively incubated with rabbit anti-M13 polyclonal antibody and horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG. Then substrate solution (0.01% H 2 O 2 and 1 mg/mL o-phenylenediamine) was added, and the reaction was stopped with 2 M sulfuric acid. The values of optical density (OD) at 490 nm was recorded. The blank control (BC), the negative control (NC) phages from G protein of porcine Vesicular Stomatitis Virus (VSV) (stored in our lab), and the positive control (PC) phages binding to EtAMA1 protein (stored in our lab) were used. Each sample was tested in triplicate. Values represent mean ± SD. Twenty-four selected phages clones showed higher binding capability than other clones (with the number of 1, 3, 13, 19, 23, 28), blank control and netative control phages ( P

    Journal: Veterinary Research

    Article Title: Specific EtMIC3-binding peptides inhibit Eimeria tenella sporozoites entry into host cells

    doi: 10.1186/s13567-020-00873-y

    Figure Lengend Snippet: Detection of binding capability between selected phages amd EtMIC3-bc1 protein. EtMIC3-bc1-coated plate was incubated with thirty selected phages. The washed plate was then successively incubated with rabbit anti-M13 polyclonal antibody and horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG. Then substrate solution (0.01% H 2 O 2 and 1 mg/mL o-phenylenediamine) was added, and the reaction was stopped with 2 M sulfuric acid. The values of optical density (OD) at 490 nm was recorded. The blank control (BC), the negative control (NC) phages from G protein of porcine Vesicular Stomatitis Virus (VSV) (stored in our lab), and the positive control (PC) phages binding to EtAMA1 protein (stored in our lab) were used. Each sample was tested in triplicate. Values represent mean ± SD. Twenty-four selected phages clones showed higher binding capability than other clones (with the number of 1, 3, 13, 19, 23, 28), blank control and netative control phages ( P

    Article Snippet: After washing, the plate was incubated with rabbit anti-EtMIC3 polyclonal antisera (60 μg/mL) diluted at 1:1000, reacted with 100 μL of HRP-labeled goat anti-rabbit IgG (1:5000) (Boster, Wuhan, China).

    Techniques: Binding Assay, Incubation, Negative Control, Positive Control, Clone Assay

    Western blot analysis of C3 and Bf in zebrafish egg cytosol (lane M: molecular marker; lane H: human serum; lane Z: zebrafish egg cytosol). The egg cytosol was electrophoresed on 12% SDS-PAGE gel using the buffer system of Laemmli. The proteins separated were blotted on nitrocellulose membrane and immunostained with rabbit anti-human C3 antibody or goat anti-human Bf antibody, followed by staining with HRP-labeled anti-rabbit IgG and HRP-labeled anti-goat IgG, respectively.

    Journal: PLoS ONE

    Article Title: Complement Activity in the Egg Cytosol of Zebrafish Danio rerio: Evidence for the Defense Role of Maternal Complement Components

    doi: 10.1371/journal.pone.0001463

    Figure Lengend Snippet: Western blot analysis of C3 and Bf in zebrafish egg cytosol (lane M: molecular marker; lane H: human serum; lane Z: zebrafish egg cytosol). The egg cytosol was electrophoresed on 12% SDS-PAGE gel using the buffer system of Laemmli. The proteins separated were blotted on nitrocellulose membrane and immunostained with rabbit anti-human C3 antibody or goat anti-human Bf antibody, followed by staining with HRP-labeled anti-rabbit IgG and HRP-labeled anti-goat IgG, respectively.

    Article Snippet: Goat anti-human C1q antibody, Rabbit anti-mouse C4 antibody and horseradish peroxidase (HRP)-labeled rabbit anti-goat IgG were from Boster (China), and HRP-labeled goat anti-rabbit IgG from Zhongshan (China).

    Techniques: Western Blot, Marker, SDS Page, Staining, Labeling