biotinylated anti-rabbit immunoglobulin Search Results


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  • 99
    Vector Laboratories biotinylated anti rabbit immunoglobulins
    Biotinylated Anti Rabbit Immunoglobulins, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 49 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biogenex biotinylated anti rabbit immunoglobulin
    Biotinylated Anti Rabbit Immunoglobulin, supplied by Biogenex, used in various techniques. Bioz Stars score: 89/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies biotinylated anti rabbit immunoglobulins
    Biotinylated Anti Rabbit Immunoglobulins, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 79 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Jackson Immuno biotinylated anti rabbit immunoglobulin
    Biotinylated Anti Rabbit Immunoglobulin, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 90/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    GE Healthcare biotinylated anti rabbit immunoglobulin
    Biotinylated Anti Rabbit Immunoglobulin, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 91/100, based on 226 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies pig anti rabbit biotinylated immunoglobulins
    Pig Anti Rabbit Biotinylated Immunoglobulins, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Abcam biotinylated chicken anti rabbit immunoglobulin
    Biotinylated Chicken Anti Rabbit Immunoglobulin, supplied by Abcam, used in various techniques. Bioz Stars score: 92/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies polyclonal rabbit anti rat immunoglobulin biotinylated ab
    Polyclonal Rabbit Anti Rat Immunoglobulin Biotinylated Ab, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies biotinylated swine anti rabbit immunoglobulin
    D11-mediated effects on the transcriptional activity of NF-κB. a Cells were treated as described in Fig. 4 and Additional file 4 : Figure S4. Subcellular localization of NF-κB was detected by immunofluorescence staining of cells with rabbit monoclonal anti-NF-κB antibody (green fluorescence, Alexa Fluor 488). Nuclei were visualized by DAPI staining. NC, negative control refers to cells stained with <t>biotinylated</t> secondary antibody and Alexa Fluor 488 streptavidin, only. Original magnification: 400x. b NF-κB transcriptional activity was determined as described in Materials and methods. The indicated cell lines were treated as described in Fig. 4 . Asterisks denote statistical significant differences in TNFα-induced NF-κB activity in the absence or presence of D11 ( N = 6, *, P
    Biotinylated Swine Anti Rabbit Immunoglobulin, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 46 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies biotinylated goat anti rabbit immunoglobulin
    D11-mediated effects on the transcriptional activity of NF-κB. a Cells were treated as described in Fig. 4 and Additional file 4 : Figure S4. Subcellular localization of NF-κB was detected by immunofluorescence staining of cells with rabbit monoclonal anti-NF-κB antibody (green fluorescence, Alexa Fluor 488). Nuclei were visualized by DAPI staining. NC, negative control refers to cells stained with <t>biotinylated</t> secondary antibody and Alexa Fluor 488 streptavidin, only. Original magnification: 400x. b NF-κB transcriptional activity was determined as described in Materials and methods. The indicated cell lines were treated as described in Fig. 4 . Asterisks denote statistical significant differences in TNFα-induced NF-κB activity in the absence or presence of D11 ( N = 6, *, P
    Biotinylated Goat Anti Rabbit Immunoglobulin, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 89/100, based on 87 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies biotinylated rabbit anti mouse immunoglobulins
    Double antibody capture ELISA demonstrating the specific binding of <t>biotinylated</t> MoAb 3B9 (○) to βA4[1–42] (b) but not βA4[1–40] (a) or βA4[1–43] (c). Biotinylated isotype control ET-1 MoAb (▪) exhibited no binding.
    Biotinylated Rabbit Anti Mouse Immunoglobulins, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 86 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Jackson Immuno biotinylated rabbit anti goat immunoglobulins
    Double antibody capture ELISA demonstrating the specific binding of <t>biotinylated</t> MoAb 3B9 (○) to βA4[1–42] (b) but not βA4[1–40] (a) or βA4[1–43] (c). Biotinylated isotype control ET-1 MoAb (▪) exhibited no binding.
    Biotinylated Rabbit Anti Goat Immunoglobulins, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 85/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies biotinylated rabbit anti rat immunoglobulins
    Double antibody capture ELISA demonstrating the specific binding of <t>biotinylated</t> MoAb 3B9 (○) to βA4[1–42] (b) but not βA4[1–40] (a) or βA4[1–43] (c). Biotinylated isotype control ET-1 MoAb (▪) exhibited no binding.
    Biotinylated Rabbit Anti Rat Immunoglobulins, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 91/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    GE Healthcare biotinylated donkey anti rabbit immunoglobulin
    Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and <t>biotinylated</t> protein standards (Amersham) (c) are indicated (lanes M).
    Biotinylated Donkey Anti Rabbit Immunoglobulin, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 88/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Vector Laboratories biotinylated anti rabbit immunoglobulin antiserum
    Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and <t>biotinylated</t> protein standards (Amersham) (c) are indicated (lanes M).
    Biotinylated Anti Rabbit Immunoglobulin Antiserum, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biogenex biotinylated goat anti rabbit immunoglobulin
    Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and <t>biotinylated</t> protein standards (Amersham) (c) are indicated (lanes M).
    Biotinylated Goat Anti Rabbit Immunoglobulin, supplied by Biogenex, used in various techniques. Bioz Stars score: 89/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher biotinylated goat anti rabbit immunoglobulins
    Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and <t>biotinylated</t> protein standards (Amersham) (c) are indicated (lanes M).
    Biotinylated Goat Anti Rabbit Immunoglobulins, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 64 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies biotinylated rabbit anti goat immunoglobulins
    Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and <t>biotinylated</t> protein standards (Amersham) (c) are indicated (lanes M).
    Biotinylated Rabbit Anti Goat Immunoglobulins, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    D11-mediated effects on the transcriptional activity of NF-κB. a Cells were treated as described in Fig. 4 and Additional file 4 : Figure S4. Subcellular localization of NF-κB was detected by immunofluorescence staining of cells with rabbit monoclonal anti-NF-κB antibody (green fluorescence, Alexa Fluor 488). Nuclei were visualized by DAPI staining. NC, negative control refers to cells stained with biotinylated secondary antibody and Alexa Fluor 488 streptavidin, only. Original magnification: 400x. b NF-κB transcriptional activity was determined as described in Materials and methods. The indicated cell lines were treated as described in Fig. 4 . Asterisks denote statistical significant differences in TNFα-induced NF-κB activity in the absence or presence of D11 ( N = 6, *, P

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: The kinase inhibitor D11 induces caspase-mediated cell death in cancer cells resistant to chemotherapeutic treatment

    doi: 10.1186/s13046-015-0234-6

    Figure Lengend Snippet: D11-mediated effects on the transcriptional activity of NF-κB. a Cells were treated as described in Fig. 4 and Additional file 4 : Figure S4. Subcellular localization of NF-κB was detected by immunofluorescence staining of cells with rabbit monoclonal anti-NF-κB antibody (green fluorescence, Alexa Fluor 488). Nuclei were visualized by DAPI staining. NC, negative control refers to cells stained with biotinylated secondary antibody and Alexa Fluor 488 streptavidin, only. Original magnification: 400x. b NF-κB transcriptional activity was determined as described in Materials and methods. The indicated cell lines were treated as described in Fig. 4 . Asterisks denote statistical significant differences in TNFα-induced NF-κB activity in the absence or presence of D11 ( N = 6, *, P

    Article Snippet: Localization of NF-κB was performed by incubating the cells with rabbit monoclonal anti-NF-κB/p65/RelA antibody (Cell Signaling Technology, Herlev, Denmark) at 4 °C overnight followed by labeling with biotinylated swine anti-rabbit immunoglobulin (Dako, Glostrup, Denmark) for 1 h at room temperature and Alexa Fluor 488-conjugated streptavidin (Life Technologies) for 30 min at room temperature.

    Techniques: Activity Assay, Immunofluorescence, Staining, Fluorescence, Negative Control

    Double antibody capture ELISA demonstrating the specific binding of biotinylated MoAb 3B9 (○) to βA4[1–42] (b) but not βA4[1–40] (a) or βA4[1–43] (c). Biotinylated isotype control ET-1 MoAb (▪) exhibited no binding.

    Journal: Clinical and Experimental Immunology

    Article Title: Identification of structural variations in the carboxyl terminus of Alzheimer's disease-associated ?A4[1-42] amyloid using a monoclonal antibody

    doi: 10.1046/j.1365-2249.2001.01209.x

    Figure Lengend Snippet: Double antibody capture ELISA demonstrating the specific binding of biotinylated MoAb 3B9 (○) to βA4[1–42] (b) but not βA4[1–40] (a) or βA4[1–43] (c). Biotinylated isotype control ET-1 MoAb (▪) exhibited no binding.

    Article Snippet: The sections were then washed three times for 5 min per wash in TBS pH 7·4 and incubated with 50 μl of biotinylated rabbit anti-mouse immunoglobulins (1:500 in TBS containing 20% (v/v) swine serum; Dako Corp., Carpinteria, CA) for a further 30 min at room temperature.

    Techniques: Enzyme-linked Immunosorbent Assay, Binding Assay

    Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and biotinylated protein standards (Amersham) (c) are indicated (lanes M).

    Journal: Journal of Virology

    Article Title: The Gene Encoding the Nucleocapsid Protein of Gill-Associated Nidovirus of Penaeus monodon Prawns Is Located Upstream of the Glycoprotein Gene

    doi: 10.1128/JVI.78.16.8935-8941.2004

    Figure Lengend Snippet: Western blot of uninfected and GAV-infected P. monodon tissues carried out with antiserum to E. coli -expressed GST-ORF2 fusion protein (a) and KLH-linked peptide PN1 (b and c). (a and b) LO (lanes 1 and 2) and gill tissues (lanes 3 and 4) from an uninfected prawn (lanes 1 and 3) and a GAV-infected prawn (lanes 2 and 4). Three proteins smaller than the ORF2 protein detected in LO tissue are indicated (◂). (c) GAV-infected gill tissue (lane 1) and the E. coli -expressed His 6 -ORF2 fusion protein (lane 2). Proteins were separated by SDS-PAGE in 12% (a and b) or 15% (c) polyacrylamide gels. The molecular masses (in kilodaltons) of prestained protein standards (Bio-Rad) (a and b) and biotinylated protein standards (Amersham) (c) are indicated (lanes M).

    Article Snippet: Western blotting was performed using a 1:200 dilution of rabbit antibody in 5% skim milk powder, and detection was carried out using a 1:1,000 dilution of biotinylated donkey anti-rabbit immunoglobulin (Amersham), a 1:1,000 dilution of streptavidin-biotin-horseradish peroxidase conjugate (Amersham), and 4-chloro-1-naphthol ( ).

    Techniques: Western Blot, Infection, SDS Page

    (a) Structural proteins (gp116, gp64, and p20) of purified YHV (lane 1) detected by staining with Coomassie blue. (b) Western blot of purified YHV (lane 1) and GAV-infected gill tissues (lane 2) with GAV GST-ORF2 antiserum. Proteins were resolved in a 12% polyacrylamide gel. Lanes M contain protein standards (a) and biotinylated protein standards (Amersham) (b), with molecular masses (in kilodaltons) indicated.

    Journal: Journal of Virology

    Article Title: The Gene Encoding the Nucleocapsid Protein of Gill-Associated Nidovirus of Penaeus monodon Prawns Is Located Upstream of the Glycoprotein Gene

    doi: 10.1128/JVI.78.16.8935-8941.2004

    Figure Lengend Snippet: (a) Structural proteins (gp116, gp64, and p20) of purified YHV (lane 1) detected by staining with Coomassie blue. (b) Western blot of purified YHV (lane 1) and GAV-infected gill tissues (lane 2) with GAV GST-ORF2 antiserum. Proteins were resolved in a 12% polyacrylamide gel. Lanes M contain protein standards (a) and biotinylated protein standards (Amersham) (b), with molecular masses (in kilodaltons) indicated.

    Article Snippet: Western blotting was performed using a 1:200 dilution of rabbit antibody in 5% skim milk powder, and detection was carried out using a 1:1,000 dilution of biotinylated donkey anti-rabbit immunoglobulin (Amersham), a 1:1,000 dilution of streptavidin-biotin-horseradish peroxidase conjugate (Amersham), and 4-chloro-1-naphthol ( ).

    Techniques: Purification, Staining, Western Blot, Infection

    Western blot of native ORF2 in GAV-infected LO and gill tissues compared to His 6 -ORF2 and N-terminally truncated His 6 -ORF2 fusion proteins expressed in E. coli . (a) GAV-infected gill tissue (lane 1) and LO tissue (lane 6) and IPTG-induced E. coli cultures transformed with pQE-ORF2 (lane 2), pQE-ORF2-M 11 (lane 3), pQE-ORF2-M 61 (lane 4), and pQE10 (lane 5) were resolved in a 15% polyacrylamide gel and immunodetected with KLH-PN1 peptide antiserum. Lane M contains biotinylated protein standards. (b and c) GAV-infected gill (lane 1) and IPTG-induced E. coli cultures transformed with pQE-ORF2 (lane 2), pQE10 (lane 3), pQE-ORF2-M 11 (lane 4), and pQE-ORF2-M 61 (lane 5) resolved in a 12% polyacrylamide gel and immunodetected using antiserum to GST-ORF2 (b) or KLH-PN1 peptide (c). Lanes M contain BenchMark prestained protein ladders (Invitrogen). The predominant His 6 -ORF2 fusion proteins (◂) and minor larger and smaller His 6 -ORF2 fusion protein forms that were also immunodetected (◃) are indicated.

    Journal: Journal of Virology

    Article Title: The Gene Encoding the Nucleocapsid Protein of Gill-Associated Nidovirus of Penaeus monodon Prawns Is Located Upstream of the Glycoprotein Gene

    doi: 10.1128/JVI.78.16.8935-8941.2004

    Figure Lengend Snippet: Western blot of native ORF2 in GAV-infected LO and gill tissues compared to His 6 -ORF2 and N-terminally truncated His 6 -ORF2 fusion proteins expressed in E. coli . (a) GAV-infected gill tissue (lane 1) and LO tissue (lane 6) and IPTG-induced E. coli cultures transformed with pQE-ORF2 (lane 2), pQE-ORF2-M 11 (lane 3), pQE-ORF2-M 61 (lane 4), and pQE10 (lane 5) were resolved in a 15% polyacrylamide gel and immunodetected with KLH-PN1 peptide antiserum. Lane M contains biotinylated protein standards. (b and c) GAV-infected gill (lane 1) and IPTG-induced E. coli cultures transformed with pQE-ORF2 (lane 2), pQE10 (lane 3), pQE-ORF2-M 11 (lane 4), and pQE-ORF2-M 61 (lane 5) resolved in a 12% polyacrylamide gel and immunodetected using antiserum to GST-ORF2 (b) or KLH-PN1 peptide (c). Lanes M contain BenchMark prestained protein ladders (Invitrogen). The predominant His 6 -ORF2 fusion proteins (◂) and minor larger and smaller His 6 -ORF2 fusion protein forms that were also immunodetected (◃) are indicated.

    Article Snippet: Western blotting was performed using a 1:200 dilution of rabbit antibody in 5% skim milk powder, and detection was carried out using a 1:1,000 dilution of biotinylated donkey anti-rabbit immunoglobulin (Amersham), a 1:1,000 dilution of streptavidin-biotin-horseradish peroxidase conjugate (Amersham), and 4-chloro-1-naphthol ( ).

    Techniques: Western Blot, Infection, Transformation Assay