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biotinylated anti il 12 c17 8  (Vector Laboratories)


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    Structured Review

    Vector Laboratories biotinylated anti il 12 c17 8
    Selective production of <t>IL-12p40</t> by the large intestine of diarrhea-induced mice. In A, large intestinal tissues from diarrhea-induced mice were immunostained with anti-IL-12p40 mAb, anti-IL-12p35 mAb, or control IgG. Control non-disease mice section gave no signal above background (data not shown). In B-1, IL-12p40-specific mRNA was expressed selectively in the large intestine of mice with allergic diarrhea. In B-2, quantitive real-time PCR analysis of IL-12p40- and p35-specific mRNA expression was performed. The ratio was obtained as the level of IL-12p40 or p35 expression in non-treated mice as a scale of one. The detailed information for the expression of this ratio is described in the Materials and Methods section. In C-E, IL-12p40 was detected in MØ and DC and epithelial cells in the large intestine. The serial sections of the large intestine from diarrhea-induced mice were stained with anti-IL-12p40 mAb and anti-CD11b mAb (C), with anti-IL-12p40 mAb and anti-CD11c mAb (D). The arrows point to double-positive cells. Large intestinal epithelial cells were stained with anti-IL-12p40 mAb (E).
    Biotinylated Anti Il 12 C17 8, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 9457 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/biotinylated anti il 12 c17 8/product/Vector Laboratories
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    1) Product Images from "Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea"

    Article Title: Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea

    Journal:

    doi:

    Selective production of IL-12p40 by the large intestine of diarrhea-induced mice. In A, large intestinal tissues from diarrhea-induced mice were immunostained with anti-IL-12p40 mAb, anti-IL-12p35 mAb, or control IgG. Control non-disease mice section gave no signal above background (data not shown). In B-1, IL-12p40-specific mRNA was expressed selectively in the large intestine of mice with allergic diarrhea. In B-2, quantitive real-time PCR analysis of IL-12p40- and p35-specific mRNA expression was performed. The ratio was obtained as the level of IL-12p40 or p35 expression in non-treated mice as a scale of one. The detailed information for the expression of this ratio is described in the Materials and Methods section. In C-E, IL-12p40 was detected in MØ and DC and epithelial cells in the large intestine. The serial sections of the large intestine from diarrhea-induced mice were stained with anti-IL-12p40 mAb and anti-CD11b mAb (C), with anti-IL-12p40 mAb and anti-CD11c mAb (D). The arrows point to double-positive cells. Large intestinal epithelial cells were stained with anti-IL-12p40 mAb (E).
    Figure Legend Snippet: Selective production of IL-12p40 by the large intestine of diarrhea-induced mice. In A, large intestinal tissues from diarrhea-induced mice were immunostained with anti-IL-12p40 mAb, anti-IL-12p35 mAb, or control IgG. Control non-disease mice section gave no signal above background (data not shown). In B-1, IL-12p40-specific mRNA was expressed selectively in the large intestine of mice with allergic diarrhea. In B-2, quantitive real-time PCR analysis of IL-12p40- and p35-specific mRNA expression was performed. The ratio was obtained as the level of IL-12p40 or p35 expression in non-treated mice as a scale of one. The detailed information for the expression of this ratio is described in the Materials and Methods section. In C-E, IL-12p40 was detected in MØ and DC and epithelial cells in the large intestine. The serial sections of the large intestine from diarrhea-induced mice were stained with anti-IL-12p40 mAb and anti-CD11b mAb (C), with anti-IL-12p40 mAb and anti-CD11c mAb (D). The arrows point to double-positive cells. Large intestinal epithelial cells were stained with anti-IL-12p40 mAb (E).

    Techniques Used: Real-time Polymerase Chain Reaction, Expressing, Staining

    Induction of IL-12p40 homodimer in the large but not small intestine of diarrhea-induced mice. Large and small intestinal tissue extracts were subjected to immunopreciptation and Western blotting analysis using anti-IL-12p40 (C17.8) mAb under non-reducing conditions (A). The captions above the figure indicate the experimental mouse group receiving different in vivo treatments. Thus, the samples were obtained from SC/PO mice treated with C17.8 or control antibodies. Further, the samples were isolated from mice treated with PO only, SC only, or non-treated mice. The arrow points to IL-12p40 homodimer expression in the large intestine of diarrhea-induced mice. The data represent four independent experiments. In B, at the indicated times after oral administration of OVA, large intestinal tissue extracts isolated from diarrhea-induced mice were assayed for IL-12p40 by the same method as in A. In C, the large intestinal tissue extracts of diarrhea-induced mice were subjected to Western blotting with anti-IL-12p35 Ab as well as anti-IL-12p40. IL-12p70 protein was used as a positive control for the IL-12p35 detection system. As negative control, immunoprecipitation was performed without the tissue specimens (Ab only). The data represent three different experiments.
    Figure Legend Snippet: Induction of IL-12p40 homodimer in the large but not small intestine of diarrhea-induced mice. Large and small intestinal tissue extracts were subjected to immunopreciptation and Western blotting analysis using anti-IL-12p40 (C17.8) mAb under non-reducing conditions (A). The captions above the figure indicate the experimental mouse group receiving different in vivo treatments. Thus, the samples were obtained from SC/PO mice treated with C17.8 or control antibodies. Further, the samples were isolated from mice treated with PO only, SC only, or non-treated mice. The arrow points to IL-12p40 homodimer expression in the large intestine of diarrhea-induced mice. The data represent four independent experiments. In B, at the indicated times after oral administration of OVA, large intestinal tissue extracts isolated from diarrhea-induced mice were assayed for IL-12p40 by the same method as in A. In C, the large intestinal tissue extracts of diarrhea-induced mice were subjected to Western blotting with anti-IL-12p35 Ab as well as anti-IL-12p40. IL-12p70 protein was used as a positive control for the IL-12p35 detection system. As negative control, immunoprecipitation was performed without the tissue specimens (Ab only). The data represent three different experiments.

    Techniques Used: Western Blot, In Vivo, Isolation, Expressing, Positive Control, Negative Control, Immunoprecipitation

    Inhibition of allergic diarrhea disease by the treatment with anti-IL-12p40 mAb. In A, anti-IL-12p40 mAb (C17.8) treatment (thin dashed line) delayed the development of allergic diarrhea when compared with the rat IgG-treated group (solid line). Statistical differences were determined by Wilcoxon rank-sum test and are indicated by **, P < 0.01. Mice with SC only were used as controls (thick dashed line). In B, left, body weight was recovered in allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). In B, right, OVA-specific IgE Abs were reduced in the serum of allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). The data are expressed as the mean of ± SE and are representative of five independent experiments. Statistical differences between anti-IL-12p40 mAb and control rat IgG-treated mice are indicated as **, P < 0.01.
    Figure Legend Snippet: Inhibition of allergic diarrhea disease by the treatment with anti-IL-12p40 mAb. In A, anti-IL-12p40 mAb (C17.8) treatment (thin dashed line) delayed the development of allergic diarrhea when compared with the rat IgG-treated group (solid line). Statistical differences were determined by Wilcoxon rank-sum test and are indicated by **, P < 0.01. Mice with SC only were used as controls (thick dashed line). In B, left, body weight was recovered in allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). In B, right, OVA-specific IgE Abs were reduced in the serum of allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). The data are expressed as the mean of ± SE and are representative of five independent experiments. Statistical differences between anti-IL-12p40 mAb and control rat IgG-treated mice are indicated as **, P < 0.01.

    Techniques Used: Inhibition

    In vivo treatment with anti-IL-12p40 (C17.8) reduced the predominant antigen-specific Th2 type responses by large intestinal mononuclear cells isolated from diarrhea-induced mice. The mononuclear cells isolated from the large intestine (1.5 × 105 cells/well) were cultured with OVA (1 mg/ml) for 3 days. Culture supernatants were harvested and then assayed for IL-4, IL-13, IL-5, and eotaxin by ELISA assay. These data are expressed as the mean ± SE and are representative of three independent experiments. The statistical differences between anti-IL-12p40 mAb and control antibody treated mice are indicated as **, P < 0.01.
    Figure Legend Snippet: In vivo treatment with anti-IL-12p40 (C17.8) reduced the predominant antigen-specific Th2 type responses by large intestinal mononuclear cells isolated from diarrhea-induced mice. The mononuclear cells isolated from the large intestine (1.5 × 105 cells/well) were cultured with OVA (1 mg/ml) for 3 days. Culture supernatants were harvested and then assayed for IL-4, IL-13, IL-5, and eotaxin by ELISA assay. These data are expressed as the mean ± SE and are representative of three independent experiments. The statistical differences between anti-IL-12p40 mAb and control antibody treated mice are indicated as **, P < 0.01.

    Techniques Used: In Vivo, Isolation, Cell Culture, Enzyme-linked Immunosorbent Assay

    Suppression of allergic diarrhea development in IL-12p40 KO mice. In A, the incidence of allergic diarrhea was reduced in the IL-12p40 KO mice when compared with wild-type mice immunized subcutaneously and then given OVA repeatedly by the oral route (SC/PO). In B, the large intestinal LP mononuclear cells from IL-12p40 KO mice did not produce IL-4. Mononuclear cells isolated from the large intestine were restimulated with OVA for the assessment of IL-4 synthesis as described in Figure 4A. The data are expressed as the mean ± SE and represent three different experiments.
    Figure Legend Snippet: Suppression of allergic diarrhea development in IL-12p40 KO mice. In A, the incidence of allergic diarrhea was reduced in the IL-12p40 KO mice when compared with wild-type mice immunized subcutaneously and then given OVA repeatedly by the oral route (SC/PO). In B, the large intestinal LP mononuclear cells from IL-12p40 KO mice did not produce IL-4. Mononuclear cells isolated from the large intestine were restimulated with OVA for the assessment of IL-4 synthesis as described in Figure 4A. The data are expressed as the mean ± SE and represent three different experiments.

    Techniques Used: Isolation



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    Selective production of <t>IL-12p40</t> by the large intestine of diarrhea-induced mice. In A, large intestinal tissues from diarrhea-induced mice were immunostained with anti-IL-12p40 mAb, anti-IL-12p35 mAb, or control IgG. Control non-disease mice section gave no signal above background (data not shown). In B-1, IL-12p40-specific mRNA was expressed selectively in the large intestine of mice with allergic diarrhea. In B-2, quantitive real-time PCR analysis of IL-12p40- and p35-specific mRNA expression was performed. The ratio was obtained as the level of IL-12p40 or p35 expression in non-treated mice as a scale of one. The detailed information for the expression of this ratio is described in the Materials and Methods section. In C-E, IL-12p40 was detected in MØ and DC and epithelial cells in the large intestine. The serial sections of the large intestine from diarrhea-induced mice were stained with anti-IL-12p40 mAb and anti-CD11b mAb (C), with anti-IL-12p40 mAb and anti-CD11c mAb (D). The arrows point to double-positive cells. Large intestinal epithelial cells were stained with anti-IL-12p40 mAb (E).
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    Image Search Results


    Selective production of IL-12p40 by the large intestine of diarrhea-induced mice. In A, large intestinal tissues from diarrhea-induced mice were immunostained with anti-IL-12p40 mAb, anti-IL-12p35 mAb, or control IgG. Control non-disease mice section gave no signal above background (data not shown). In B-1, IL-12p40-specific mRNA was expressed selectively in the large intestine of mice with allergic diarrhea. In B-2, quantitive real-time PCR analysis of IL-12p40- and p35-specific mRNA expression was performed. The ratio was obtained as the level of IL-12p40 or p35 expression in non-treated mice as a scale of one. The detailed information for the expression of this ratio is described in the Materials and Methods section. In C-E, IL-12p40 was detected in MØ and DC and epithelial cells in the large intestine. The serial sections of the large intestine from diarrhea-induced mice were stained with anti-IL-12p40 mAb and anti-CD11b mAb (C), with anti-IL-12p40 mAb and anti-CD11c mAb (D). The arrows point to double-positive cells. Large intestinal epithelial cells were stained with anti-IL-12p40 mAb (E).

    Journal:

    Article Title: Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea

    doi:

    Figure Lengend Snippet: Selective production of IL-12p40 by the large intestine of diarrhea-induced mice. In A, large intestinal tissues from diarrhea-induced mice were immunostained with anti-IL-12p40 mAb, anti-IL-12p35 mAb, or control IgG. Control non-disease mice section gave no signal above background (data not shown). In B-1, IL-12p40-specific mRNA was expressed selectively in the large intestine of mice with allergic diarrhea. In B-2, quantitive real-time PCR analysis of IL-12p40- and p35-specific mRNA expression was performed. The ratio was obtained as the level of IL-12p40 or p35 expression in non-treated mice as a scale of one. The detailed information for the expression of this ratio is described in the Materials and Methods section. In C-E, IL-12p40 was detected in MØ and DC and epithelial cells in the large intestine. The serial sections of the large intestine from diarrhea-induced mice were stained with anti-IL-12p40 mAb and anti-CD11b mAb (C), with anti-IL-12p40 mAb and anti-CD11c mAb (D). The arrows point to double-positive cells. Large intestinal epithelial cells were stained with anti-IL-12p40 mAb (E).

    Article Snippet: After electrophoresis, proteins were transferred to a polyvinylidene difluoride microporous membrane (PVDF Immobilon; Millipore, Bedford, MA) and the membrane was reacted with biotinylated anti-IL-12 (C17.8) followed by incubation with biotin-streptavidin complex (ABC-AP Kit; Vector Laboratories, Inc.).

    Techniques: Real-time Polymerase Chain Reaction, Expressing, Staining

    Induction of IL-12p40 homodimer in the large but not small intestine of diarrhea-induced mice. Large and small intestinal tissue extracts were subjected to immunopreciptation and Western blotting analysis using anti-IL-12p40 (C17.8) mAb under non-reducing conditions (A). The captions above the figure indicate the experimental mouse group receiving different in vivo treatments. Thus, the samples were obtained from SC/PO mice treated with C17.8 or control antibodies. Further, the samples were isolated from mice treated with PO only, SC only, or non-treated mice. The arrow points to IL-12p40 homodimer expression in the large intestine of diarrhea-induced mice. The data represent four independent experiments. In B, at the indicated times after oral administration of OVA, large intestinal tissue extracts isolated from diarrhea-induced mice were assayed for IL-12p40 by the same method as in A. In C, the large intestinal tissue extracts of diarrhea-induced mice were subjected to Western blotting with anti-IL-12p35 Ab as well as anti-IL-12p40. IL-12p70 protein was used as a positive control for the IL-12p35 detection system. As negative control, immunoprecipitation was performed without the tissue specimens (Ab only). The data represent three different experiments.

    Journal:

    Article Title: Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea

    doi:

    Figure Lengend Snippet: Induction of IL-12p40 homodimer in the large but not small intestine of diarrhea-induced mice. Large and small intestinal tissue extracts were subjected to immunopreciptation and Western blotting analysis using anti-IL-12p40 (C17.8) mAb under non-reducing conditions (A). The captions above the figure indicate the experimental mouse group receiving different in vivo treatments. Thus, the samples were obtained from SC/PO mice treated with C17.8 or control antibodies. Further, the samples were isolated from mice treated with PO only, SC only, or non-treated mice. The arrow points to IL-12p40 homodimer expression in the large intestine of diarrhea-induced mice. The data represent four independent experiments. In B, at the indicated times after oral administration of OVA, large intestinal tissue extracts isolated from diarrhea-induced mice were assayed for IL-12p40 by the same method as in A. In C, the large intestinal tissue extracts of diarrhea-induced mice were subjected to Western blotting with anti-IL-12p35 Ab as well as anti-IL-12p40. IL-12p70 protein was used as a positive control for the IL-12p35 detection system. As negative control, immunoprecipitation was performed without the tissue specimens (Ab only). The data represent three different experiments.

    Article Snippet: After electrophoresis, proteins were transferred to a polyvinylidene difluoride microporous membrane (PVDF Immobilon; Millipore, Bedford, MA) and the membrane was reacted with biotinylated anti-IL-12 (C17.8) followed by incubation with biotin-streptavidin complex (ABC-AP Kit; Vector Laboratories, Inc.).

    Techniques: Western Blot, In Vivo, Isolation, Expressing, Positive Control, Negative Control, Immunoprecipitation

    Inhibition of allergic diarrhea disease by the treatment with anti-IL-12p40 mAb. In A, anti-IL-12p40 mAb (C17.8) treatment (thin dashed line) delayed the development of allergic diarrhea when compared with the rat IgG-treated group (solid line). Statistical differences were determined by Wilcoxon rank-sum test and are indicated by **, P < 0.01. Mice with SC only were used as controls (thick dashed line). In B, left, body weight was recovered in allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). In B, right, OVA-specific IgE Abs were reduced in the serum of allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). The data are expressed as the mean of ± SE and are representative of five independent experiments. Statistical differences between anti-IL-12p40 mAb and control rat IgG-treated mice are indicated as **, P < 0.01.

    Journal:

    Article Title: Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea

    doi:

    Figure Lengend Snippet: Inhibition of allergic diarrhea disease by the treatment with anti-IL-12p40 mAb. In A, anti-IL-12p40 mAb (C17.8) treatment (thin dashed line) delayed the development of allergic diarrhea when compared with the rat IgG-treated group (solid line). Statistical differences were determined by Wilcoxon rank-sum test and are indicated by **, P < 0.01. Mice with SC only were used as controls (thick dashed line). In B, left, body weight was recovered in allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). In B, right, OVA-specific IgE Abs were reduced in the serum of allergic diarrhea mice treated with anti-IL-12p40 mAb (C17.8). The data are expressed as the mean of ± SE and are representative of five independent experiments. Statistical differences between anti-IL-12p40 mAb and control rat IgG-treated mice are indicated as **, P < 0.01.

    Article Snippet: After electrophoresis, proteins were transferred to a polyvinylidene difluoride microporous membrane (PVDF Immobilon; Millipore, Bedford, MA) and the membrane was reacted with biotinylated anti-IL-12 (C17.8) followed by incubation with biotin-streptavidin complex (ABC-AP Kit; Vector Laboratories, Inc.).

    Techniques: Inhibition

    In vivo treatment with anti-IL-12p40 (C17.8) reduced the predominant antigen-specific Th2 type responses by large intestinal mononuclear cells isolated from diarrhea-induced mice. The mononuclear cells isolated from the large intestine (1.5 × 105 cells/well) were cultured with OVA (1 mg/ml) for 3 days. Culture supernatants were harvested and then assayed for IL-4, IL-13, IL-5, and eotaxin by ELISA assay. These data are expressed as the mean ± SE and are representative of three independent experiments. The statistical differences between anti-IL-12p40 mAb and control antibody treated mice are indicated as **, P < 0.01.

    Journal:

    Article Title: Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea

    doi:

    Figure Lengend Snippet: In vivo treatment with anti-IL-12p40 (C17.8) reduced the predominant antigen-specific Th2 type responses by large intestinal mononuclear cells isolated from diarrhea-induced mice. The mononuclear cells isolated from the large intestine (1.5 × 105 cells/well) were cultured with OVA (1 mg/ml) for 3 days. Culture supernatants were harvested and then assayed for IL-4, IL-13, IL-5, and eotaxin by ELISA assay. These data are expressed as the mean ± SE and are representative of three independent experiments. The statistical differences between anti-IL-12p40 mAb and control antibody treated mice are indicated as **, P < 0.01.

    Article Snippet: After electrophoresis, proteins were transferred to a polyvinylidene difluoride microporous membrane (PVDF Immobilon; Millipore, Bedford, MA) and the membrane was reacted with biotinylated anti-IL-12 (C17.8) followed by incubation with biotin-streptavidin complex (ABC-AP Kit; Vector Laboratories, Inc.).

    Techniques: In Vivo, Isolation, Cell Culture, Enzyme-linked Immunosorbent Assay

    Suppression of allergic diarrhea development in IL-12p40 KO mice. In A, the incidence of allergic diarrhea was reduced in the IL-12p40 KO mice when compared with wild-type mice immunized subcutaneously and then given OVA repeatedly by the oral route (SC/PO). In B, the large intestinal LP mononuclear cells from IL-12p40 KO mice did not produce IL-4. Mononuclear cells isolated from the large intestine were restimulated with OVA for the assessment of IL-4 synthesis as described in Figure 4A. The data are expressed as the mean ± SE and represent three different experiments.

    Journal:

    Article Title: Pathological Role of Large Intestinal IL-12p40 for the Induction of Th2-Type Allergic Diarrhea

    doi:

    Figure Lengend Snippet: Suppression of allergic diarrhea development in IL-12p40 KO mice. In A, the incidence of allergic diarrhea was reduced in the IL-12p40 KO mice when compared with wild-type mice immunized subcutaneously and then given OVA repeatedly by the oral route (SC/PO). In B, the large intestinal LP mononuclear cells from IL-12p40 KO mice did not produce IL-4. Mononuclear cells isolated from the large intestine were restimulated with OVA for the assessment of IL-4 synthesis as described in Figure 4A. The data are expressed as the mean ± SE and represent three different experiments.

    Article Snippet: After electrophoresis, proteins were transferred to a polyvinylidene difluoride microporous membrane (PVDF Immobilon; Millipore, Bedford, MA) and the membrane was reacted with biotinylated anti-IL-12 (C17.8) followed by incubation with biotin-streptavidin complex (ABC-AP Kit; Vector Laboratories, Inc.).

    Techniques: Isolation