peroxidase conjugated anti rabbit  (Boster Bio)


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    Boster Bio peroxidase conjugated anti rabbit
    Peroxidase Conjugated Anti Rabbit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/peroxidase conjugated anti rabbit/product/Boster Bio
    Average 94 stars, based on 7 article reviews
    Price from $9.99 to $1999.99
    peroxidase conjugated anti rabbit - by Bioz Stars, 2022-08
    94/100 stars

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  • 94
    Boster Bio hrp conjugated anti rabbit igg sabc kit
    Immunohistochemistry (IHC) staining of PSCK isozymes in various tissues after bacterial infection. The size bars indicate 30 μm for A, B and E; 150 μm for C and D. CMN, cardiac myocytes nuclear; FbN, fibroblast nuclear; MF, Myocardial fiber; KC, Kupffer's cells; HN, Hepatocyte nuclear; RP, red pulp; WP, white pulp; CA, central artery; SN, splenic nodule; PLS; periarterial lymphatic sheath; PCT, proximal convoluted tubule; DCT, distal convoluted tubule; G, glomus; IV, interlobular veins; SMF, skeletal muscle fiber. The primary antibody was used as CK-B (1:100), CK-M (1:100) and CK-S (1:100). The sections were incubated with Rabbit <t>IgG</t> <t>SABC</t> Kit (Boster, Wuhan, China, SA1022). Reaction products were visualized by addition of chromogenic substrate 0.1% diaminobenzidine solution (Sigma-Aldrich, St. Louis, MO, USA) in 0.1% hydrogen peroxide in PBS and the slides counterstained with Harris hematoxylin lightly. The slides finally were examined by light microscopy (Nikon 80i, Tokyo, Japan). Negative controls were performed with diluent normal rabbit serum (1:500) instead of the primary antibody.
    Hrp Conjugated Anti Rabbit Igg Sabc Kit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hrp conjugated anti rabbit igg sabc kit/product/Boster Bio
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hrp conjugated anti rabbit igg sabc kit - by Bioz Stars, 2022-08
    94/100 stars
      Buy from Supplier

    86
    Boster Bio hrp conjugated spa
    Identification the binding of pIgG or hIgG to IBPs of S. suis 2 by Far-western blot. SDS-PAGE ( a , c ) and Far-western blot analysis ( b , d ) of the S. suis 2 recombinant IBPs. Recombinant proteins (Enolase, LysM, Pyk, LDH, FBA, KAR) and casein were subjected to SDS-PAGE, then transferred onto PVDF membranes and incubated with pIgG or hIgG. Bound pIgG or hIgG was recognized with <t>HRP</t> conjugated <t>SPA.</t> Casein was used as a negative control for non-specific binding to IgG
    Hrp Conjugated Spa, supplied by Boster Bio, 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/hrp conjugated spa/product/Boster Bio
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hrp conjugated spa - by Bioz Stars, 2022-08
    86/100 stars
      Buy from Supplier

    94
    Boster Bio peroxidase conjugated goat anti rabbit immunoglobulin g igg
    Anti-IFN-γ reduces acute brain injury in aging ICH rats. (A) The neurological deficit scores of 22-month-old ICH rats after treatment with anti-IFN-γ antibody or normal <t>IgG</t> ( n = 12). (B) The mortality of aging ICH rats after treatment with anti-IFN-γ antibody or normal IgG ( n = 20). (C) Level of brain water contents in perihematomal brain tissues in 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG ( n = 4). (D) Hematoxylin and eosin (H E) staining of perihematomal brain tissue derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 200 μm at the top and 100 μm at the bottom. (E) Fluoro-Jade B (FJB) staining and quantification of degenerative neural cells in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with an anti-IFN-γ antibody or normal IgG. Scale bars, 100 μm at the top and 50 μm at the bottom. (F) TUNEL assay and quantification of apoptotic neural cells in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 100 μm at the top and 50 μm at the bottom. (G) Nissl staining and quantification of Nissl bodies in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 200 μm at the top and 50 μm at the bottom. The bar graphs show the mean ± SEM. p -value determined using the Student's t -test. * p
    Peroxidase Conjugated Goat Anti Rabbit Immunoglobulin G Igg, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/peroxidase conjugated goat anti rabbit immunoglobulin g igg/product/Boster Bio
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    peroxidase conjugated goat anti rabbit immunoglobulin g igg - by Bioz Stars, 2022-08
    94/100 stars
      Buy from Supplier

    97
    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, 2022-08
    97/100 stars
      Buy from Supplier

    Image Search Results


    Immunohistochemistry (IHC) staining of PSCK isozymes in various tissues after bacterial infection. The size bars indicate 30 μm for A, B and E; 150 μm for C and D. CMN, cardiac myocytes nuclear; FbN, fibroblast nuclear; MF, Myocardial fiber; KC, Kupffer's cells; HN, Hepatocyte nuclear; RP, red pulp; WP, white pulp; CA, central artery; SN, splenic nodule; PLS; periarterial lymphatic sheath; PCT, proximal convoluted tubule; DCT, distal convoluted tubule; G, glomus; IV, interlobular veins; SMF, skeletal muscle fiber. The primary antibody was used as CK-B (1:100), CK-M (1:100) and CK-S (1:100). The sections were incubated with Rabbit IgG SABC Kit (Boster, Wuhan, China, SA1022). Reaction products were visualized by addition of chromogenic substrate 0.1% diaminobenzidine solution (Sigma-Aldrich, St. Louis, MO, USA) in 0.1% hydrogen peroxide in PBS and the slides counterstained with Harris hematoxylin lightly. The slides finally were examined by light microscopy (Nikon 80i, Tokyo, Japan). Negative controls were performed with diluent normal rabbit serum (1:500) instead of the primary antibody.

    Journal: International Journal of Biological Macromolecules

    Article Title: Comparative studies of the expression of creatine kinase isoforms under immune stress in Pelodiscus sinensis

    doi: 10.1016/j.ijbiomac.2020.06.036

    Figure Lengend Snippet: Immunohistochemistry (IHC) staining of PSCK isozymes in various tissues after bacterial infection. The size bars indicate 30 μm for A, B and E; 150 μm for C and D. CMN, cardiac myocytes nuclear; FbN, fibroblast nuclear; MF, Myocardial fiber; KC, Kupffer's cells; HN, Hepatocyte nuclear; RP, red pulp; WP, white pulp; CA, central artery; SN, splenic nodule; PLS; periarterial lymphatic sheath; PCT, proximal convoluted tubule; DCT, distal convoluted tubule; G, glomus; IV, interlobular veins; SMF, skeletal muscle fiber. The primary antibody was used as CK-B (1:100), CK-M (1:100) and CK-S (1:100). The sections were incubated with Rabbit IgG SABC Kit (Boster, Wuhan, China, SA1022). Reaction products were visualized by addition of chromogenic substrate 0.1% diaminobenzidine solution (Sigma-Aldrich, St. Louis, MO, USA) in 0.1% hydrogen peroxide in PBS and the slides counterstained with Harris hematoxylin lightly. The slides finally were examined by light microscopy (Nikon 80i, Tokyo, Japan). Negative controls were performed with diluent normal rabbit serum (1:500) instead of the primary antibody.

    Article Snippet: After rinsing with 0.01 M PBS, the sections were incubated with Rabbit IgG SABC Kit (Boster, Wuhan, China, SA1022).

    Techniques: Immunohistochemistry, Staining, Infection, Incubation, Light Microscopy

    Identification the binding of pIgG or hIgG to IBPs of S. suis 2 by Far-western blot. SDS-PAGE ( a , c ) and Far-western blot analysis ( b , d ) of the S. suis 2 recombinant IBPs. Recombinant proteins (Enolase, LysM, Pyk, LDH, FBA, KAR) and casein were subjected to SDS-PAGE, then transferred onto PVDF membranes and incubated with pIgG or hIgG. Bound pIgG or hIgG was recognized with HRP conjugated SPA. Casein was used as a negative control for non-specific binding to IgG

    Journal: AMB Express

    Article Title: Identification of novel pig and human immunoglobulin G-binding proteins and characterization of the binding regions of enolase from Streptococcus suis serotype 2

    doi: 10.1186/s13568-020-01042-2

    Figure Lengend Snippet: Identification the binding of pIgG or hIgG to IBPs of S. suis 2 by Far-western blot. SDS-PAGE ( a , c ) and Far-western blot analysis ( b , d ) of the S. suis 2 recombinant IBPs. Recombinant proteins (Enolase, LysM, Pyk, LDH, FBA, KAR) and casein were subjected to SDS-PAGE, then transferred onto PVDF membranes and incubated with pIgG or hIgG. Bound pIgG or hIgG was recognized with HRP conjugated SPA. Casein was used as a negative control for non-specific binding to IgG

    Article Snippet: Subsequently, the membranes were washed three times with the washing buffer TBST and incubated with HRP conjugated SPA (Boster; 0.2 µg/ml) for 1 h at 37 °C.

    Techniques: Binding Assay, Far Western Blot, SDS Page, Recombinant, Incubation, Negative Control

    Identification the binding of pIgG or hIgG to IBPs of S. suis 2 by dot blot. Recombinant pIBPs ( a ) and hIBPs ( b ) were spotted onto the methanol-activated PVDF membranes and incubated with pIgG or hIgG. Bound pIgG or hIgG was recognized with HRP conjugated SPA. Casein was used as a negative control for non-specific binding to IgG and the membrane with HRP conjugated SPA alone were used as a blank control

    Journal: AMB Express

    Article Title: Identification of novel pig and human immunoglobulin G-binding proteins and characterization of the binding regions of enolase from Streptococcus suis serotype 2

    doi: 10.1186/s13568-020-01042-2

    Figure Lengend Snippet: Identification the binding of pIgG or hIgG to IBPs of S. suis 2 by dot blot. Recombinant pIBPs ( a ) and hIBPs ( b ) were spotted onto the methanol-activated PVDF membranes and incubated with pIgG or hIgG. Bound pIgG or hIgG was recognized with HRP conjugated SPA. Casein was used as a negative control for non-specific binding to IgG and the membrane with HRP conjugated SPA alone were used as a blank control

    Article Snippet: Subsequently, the membranes were washed three times with the washing buffer TBST and incubated with HRP conjugated SPA (Boster; 0.2 µg/ml) for 1 h at 37 °C.

    Techniques: Binding Assay, Dot Blot, Recombinant, Incubation, Negative Control

    2-DE profiles and Far-western blot to identify the affinity of pIgG and hIgG interactions with S. suis 2 cell wall and extracellular proteins. The cell wall and extracellular proteins of S. suis 2 were loaded into immobilized pH gradient strips for IEF analysis and by SDS-PAGE in the second dimension. The 2-DE gels were transferred onto PVDF membranes and incubated with pIgG or hIgG. Arrows indicate pIBPs or hIBPs detected with HRP conjugated SPA. a 2-DE gel of S. suis 2 extracellular proteins. b Far-western blot of extracellular proteins incubated with pIgG. c Far-western blot of extracellular proteins incubated with hIgG. d 2-DE gel of S. suis 2 cell wall proteins. e Far-western blot of cell wall proteins incubated with pIgG. f Far-western blot of cell wall proteins incubated with hIgG

    Journal: AMB Express

    Article Title: Identification of novel pig and human immunoglobulin G-binding proteins and characterization of the binding regions of enolase from Streptococcus suis serotype 2

    doi: 10.1186/s13568-020-01042-2

    Figure Lengend Snippet: 2-DE profiles and Far-western blot to identify the affinity of pIgG and hIgG interactions with S. suis 2 cell wall and extracellular proteins. The cell wall and extracellular proteins of S. suis 2 were loaded into immobilized pH gradient strips for IEF analysis and by SDS-PAGE in the second dimension. The 2-DE gels were transferred onto PVDF membranes and incubated with pIgG or hIgG. Arrows indicate pIBPs or hIBPs detected with HRP conjugated SPA. a 2-DE gel of S. suis 2 extracellular proteins. b Far-western blot of extracellular proteins incubated with pIgG. c Far-western blot of extracellular proteins incubated with hIgG. d 2-DE gel of S. suis 2 cell wall proteins. e Far-western blot of cell wall proteins incubated with pIgG. f Far-western blot of cell wall proteins incubated with hIgG

    Article Snippet: Subsequently, the membranes were washed three times with the washing buffer TBST and incubated with HRP conjugated SPA (Boster; 0.2 µg/ml) for 1 h at 37 °C.

    Techniques: Far Western Blot, Electrofocusing, SDS Page, Incubation

    Anti-IFN-γ reduces acute brain injury in aging ICH rats. (A) The neurological deficit scores of 22-month-old ICH rats after treatment with anti-IFN-γ antibody or normal IgG ( n = 12). (B) The mortality of aging ICH rats after treatment with anti-IFN-γ antibody or normal IgG ( n = 20). (C) Level of brain water contents in perihematomal brain tissues in 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG ( n = 4). (D) Hematoxylin and eosin (H E) staining of perihematomal brain tissue derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 200 μm at the top and 100 μm at the bottom. (E) Fluoro-Jade B (FJB) staining and quantification of degenerative neural cells in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with an anti-IFN-γ antibody or normal IgG. Scale bars, 100 μm at the top and 50 μm at the bottom. (F) TUNEL assay and quantification of apoptotic neural cells in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 100 μm at the top and 50 μm at the bottom. (G) Nissl staining and quantification of Nissl bodies in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 200 μm at the top and 50 μm at the bottom. The bar graphs show the mean ± SEM. p -value determined using the Student's t -test. * p

    Journal: Frontiers in Neuroscience

    Article Title: Redistribution of Histone Marks on Inflammatory Genes Associated With Intracerebral Hemorrhage-Induced Acute Brain Injury in Aging Rats

    doi: 10.3389/fnins.2022.639656

    Figure Lengend Snippet: Anti-IFN-γ reduces acute brain injury in aging ICH rats. (A) The neurological deficit scores of 22-month-old ICH rats after treatment with anti-IFN-γ antibody or normal IgG ( n = 12). (B) The mortality of aging ICH rats after treatment with anti-IFN-γ antibody or normal IgG ( n = 20). (C) Level of brain water contents in perihematomal brain tissues in 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG ( n = 4). (D) Hematoxylin and eosin (H E) staining of perihematomal brain tissue derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 200 μm at the top and 100 μm at the bottom. (E) Fluoro-Jade B (FJB) staining and quantification of degenerative neural cells in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with an anti-IFN-γ antibody or normal IgG. Scale bars, 100 μm at the top and 50 μm at the bottom. (F) TUNEL assay and quantification of apoptotic neural cells in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 100 μm at the top and 50 μm at the bottom. (G) Nissl staining and quantification of Nissl bodies in perihematomal brain tissues derived from 22-month-old ICH rats 3 days after treatment with anti-IFN-γ antibody or normal IgG. Scale bars, 200 μm at the top and 50 μm at the bottom. The bar graphs show the mean ± SEM. p -value determined using the Student's t -test. * p

    Article Snippet: On the following day, the sections were washed with PBS three times and then incubated with horseradish peroxidase-conjugated goat anti-rabbit immunoglobulin G (IgG) (Boster, Beijing, China) at a dilution of 1:500 for 1 h at 37°C.

    Techniques: Staining, Derivative Assay, TUNEL Assay

    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