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polyclonal rabbit anti-mouse socs3  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc polyclonal rabbit anti-mouse socs3
    IL-6 production by cDC1 and cDC2 regulates differential IDO1 expression (A) Gene expression microarray analysis of cDC1 and cDC2 untreated or treated with LPS (250 ng/mL) for 24 h. Bright blue (lowest) to bright red (highest). (B) Heatmap of cytokines in supernatants from cDC1 and cDC2 cultures treated as (A) (n = 2). (C) IL-6-fold induction in LPS (250 ng/mL) stimulated cDC1 and cDC2 over the untreated control (n = 3). (D) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 3). (E) <t>SOCS3</t> immunoblot in cDC1 and cDC2 treated as depicted for 24 h (n = 3). (F) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 4). (G) Analysis of skin reactivity is presented as change in footpad weight. n = 6 mice per group (n = 2). (H) EAE score of mixed bone marrow chimeras with bone marrow of indicated genotypes. 6 mice per group, n = 2. Data are shown as means ± SD. ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, two-way ANOVA followed by Bonferroni multiple comparison test (C and H) or Tukey’s multiple comparison test (G). β-Actin used as loading control (D–F). Please also see <xref ref-type=Figure S4 . " width="250" height="auto" />
    Polyclonal Rabbit Anti Mouse Socs3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+socs3+antibody/socs3+antibody/pmc09220322-67-0-5
    Average 90 stars, based on 1 article reviews
    polyclonal rabbit anti-mouse socs3 - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Indoleamine 2,3-dioxygenase 1 activation in mature cDC1 promotes tolerogenic education of inflammatory cDC2 via metabolic communication"

    Article Title: Indoleamine 2,3-dioxygenase 1 activation in mature cDC1 promotes tolerogenic education of inflammatory cDC2 via metabolic communication

    Journal: Immunity

    doi: 10.1016/j.immuni.2022.05.013

    IL-6 production by cDC1 and cDC2 regulates differential IDO1 expression (A) Gene expression microarray analysis of cDC1 and cDC2 untreated or treated with LPS (250 ng/mL) for 24 h. Bright blue (lowest) to bright red (highest). (B) Heatmap of cytokines in supernatants from cDC1 and cDC2 cultures treated as (A) (n = 2). (C) IL-6-fold induction in LPS (250 ng/mL) stimulated cDC1 and cDC2 over the untreated control (n = 3). (D) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 3). (E) SOCS3 immunoblot in cDC1 and cDC2 treated as depicted for 24 h (n = 3). (F) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 4). (G) Analysis of skin reactivity is presented as change in footpad weight. n = 6 mice per group (n = 2). (H) EAE score of mixed bone marrow chimeras with bone marrow of indicated genotypes. 6 mice per group, n = 2. Data are shown as means ± SD. ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, two-way ANOVA followed by Bonferroni multiple comparison test (C and H) or Tukey’s multiple comparison test (G). β-Actin used as loading control (D–F). Please also see <xref ref-type=Figure S4 . " title="... depicted for 48 h (n = 3). (E) SOCS3 immunoblot in cDC1 and cDC2 treated as depicted ..." property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: IL-6 production by cDC1 and cDC2 regulates differential IDO1 expression (A) Gene expression microarray analysis of cDC1 and cDC2 untreated or treated with LPS (250 ng/mL) for 24 h. Bright blue (lowest) to bright red (highest). (B) Heatmap of cytokines in supernatants from cDC1 and cDC2 cultures treated as (A) (n = 2). (C) IL-6-fold induction in LPS (250 ng/mL) stimulated cDC1 and cDC2 over the untreated control (n = 3). (D) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 3). (E) SOCS3 immunoblot in cDC1 and cDC2 treated as depicted for 24 h (n = 3). (F) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 4). (G) Analysis of skin reactivity is presented as change in footpad weight. n = 6 mice per group (n = 2). (H) EAE score of mixed bone marrow chimeras with bone marrow of indicated genotypes. 6 mice per group, n = 2. Data are shown as means ± SD. ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, two-way ANOVA followed by Bonferroni multiple comparison test (C and H) or Tukey’s multiple comparison test (G). β-Actin used as loading control (D–F). Please also see Figure S4 .

    Techniques Used: Expressing, Gene Expression, Microarray, Control, Western Blot, Comparison


    Figure Legend Snippet:

    Techniques Used: Produced, Virus, Subcloning, Recombinant, Electron Microscopy, Protease Inhibitor, Purification, Adjuvant, Modification, Selection, Western Blot, In Situ, Enzyme-linked Immunosorbent Assay, Reverse Transcription, SYBR Green Assay, Bradford Protein Assay, Control, Retroviral, Mouse Assay, Sequencing, Real-time Polymerase Chain Reaction, Cloning, Software

    Related Articles

    Incubation:

    Article Title: Inactivation of Socs3 in the Hypothalamus Enhances the Hindbrain Response to Endogenous Satiety Signals via Oxytocin Signaling
    Article Snippet: .. Membranes were then blocked in 20 m m Tris buffer, pH 7.4, containing 5% bovine serum albumin and 0.1% Tween 20 and incubated with a rabbit polyclonal anti-Socs3 antibody (1:1000; Cell Signaling Technology) overnight at 4°C. .. Membranes were then washed three times and incubated 2 h with anti-rabbit horseradish peroxidase (HRP)-conjugated secondary antibodies (1:2000; DAKO), washed again, developed by enhanced chemiluminescence (ECL substrate; Pierce), and exposed to Kodak BioMax films.

    Article Title: Inactivation of Socs3 in the Hypothalamus Enhances the Hindbrain Response to Endogenous Satiety Signals via Oxytocin Signaling
    Article Snippet: .. Membranes were then blocked in 20 mM Tris buffer, pH 7.4, containing 5% bovine serum albumin and 0.1% Tween 20 and incubated with a rabbit polyclonal anti-Socs3 antibody (1:1000; Cell Signaling Technology) overnight at 4°C. .. Membranes were then washed three times and incubated 2 h with anti-rabbit horseradish peroxidase (HRP)conjugated secondary antibodies (1:2000; DAKO), washed again, devel- oped by enhanced chemiluminescence (ECL substrate; Pierce), and exposed to Kodak BioMax films.

    Article Title: Allomyrina Dichotoma Larvae Regulate Food Intake and Body Weight in High Fat Diet-Induced Obese Mice Through mTOR and Mapk Signaling Pathways
    Article Snippet: Equal amounts of protein were separated by 8% or 12% SDS-PAGE and transferred to PVDF membranes (Bio-rad, Hercules, CA, USA). .. Membranes were blocked with 5% skim milk and sequentially incubated with primary antibodies (mouse monoclonal anti-CHOP antibody (1:1000; Cell Signaling Technology, Danvers, MA, USA); rabbit polyclonal anti-phospho-eIF2α antibody (1:1000; Cell Signaling Technology, Danvers, MA, USA); rabbit polyclonal anti-eIF2α antibody (1:1000; Cell Signaling Technology, Danvers, MA, USA); mouse monoclonal anti-Ero1L antibody (1:1000; Abnova, Taipei, Taiwan); mouse monoclonal anti-PDI antibody (1:1000; Enzo Life Sciences, Inc., Plymouth Meeting, PA, USA); rabbit monoclonal anti-phospho-Stat3 (Tyr705) (1:1000; Cell Signaling Technology, Danvers, MA, USA); mouse monoclonal anti-Stat3 (1:1000; Cell Signaling Technology, Danvers, MA, USA); rabbit polyclonal anti-SOCS3 antibody (1:1000; Cell Signaling Technology, Danvers, MA, USA); α-tubulin antibody (1:2000; Sigma-Aldrich, St Louis, MO, USA), and HRP-conjugated secondary antibody (1:10,000; anti-mouse and rabbit-IgG antibody; Amersham Biosceinces, Piscataway, NJ, USA )), followed by detection using an ECL detection kit (Invitrogen, Waltham, MA, USA). .. Total RNA was extracted from tissue or cells with an RNeasy Mini Kit (Qiagen, Hilden, Germany), according to the manufacturer’s instructions.

    other:

    Article Title: Inactivation of Socs3 in the Hypothalamus Enhances the Hindbrain Response to Endogenous Satiety Signals via Oxytocin Signaling
    Article Snippet: Membranes were then washed three times and incubated 2 h with anti-rabbit horseradish peroxidase (HRP)-conjugated secondary antibodies (1:2000; DAKO), washed again, developed by enhanced chemiluminescence (ECL substrate; Pierce), and exposed to Kodak BioMax films.



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    Image Search Results


    PCV2 infection upregulated the mRNA and protein levels of SOCS3 in PK-15 cells. ( a ) PK-15 cells were inoculated with PCV2 at a MOI of 1.0 or mock-infected for 0, 12, 24, and 48 h and analyzed by qRT-PCR measurements of the SOCS3 mRNA. ( b ) Immunoblotting with anti-SOCS3 and anti-β-actin antibodies to measure the SOCS3 protein at 0, 12, 24, and 48 hpi, respectively. Data are presented as mean ± SD ( n = 3). * p < 0.05, *** p < 0.001 vs. control.

    Journal: Viruses

    Article Title: PCV2 Infection Upregulates SOCS3 Expression to Facilitate Viral Replication in PK-15 Cells

    doi: 10.3390/v17081081

    Figure Lengend Snippet: PCV2 infection upregulated the mRNA and protein levels of SOCS3 in PK-15 cells. ( a ) PK-15 cells were inoculated with PCV2 at a MOI of 1.0 or mock-infected for 0, 12, 24, and 48 h and analyzed by qRT-PCR measurements of the SOCS3 mRNA. ( b ) Immunoblotting with anti-SOCS3 and anti-β-actin antibodies to measure the SOCS3 protein at 0, 12, 24, and 48 hpi, respectively. Data are presented as mean ± SD ( n = 3). * p < 0.05, *** p < 0.001 vs. control.

    Article Snippet: Immunoblotting was performed using a rabbit polyclonal anti-SOCS3 antibody (Proteintech; 1:1000 dilution) incubated overnight at 4 °C, followed by incubation with a HRP-conjugated goat anti-rabbit secondary antibody (Servicebio; 1:3000 dilution) for 1 h at room temperature.

    Techniques: Infection, Quantitative RT-PCR, Western Blot, Control

    SOCS3 expression facilitates PCV2 replication. ( a ) Fluorescence imaging of PK-15 cells transfected with varying concentrations of Cy3-labeled siRNA. ( b ) SOCS3 mRNA expression levels and ( c ) corresponding knockdown efficiency at different time points post-siRNA transfection. ( d ) Fluorescence visualization of HEK-293T cells at distinct time intervals following lentiviral vector transduction. ( e ) Fluorescence patterns of SOCS3-stably transfected cells and blank controls after 10 consecutive passages. ( f ) Relative SOCS3 mRNA expression levels in stably transfected cells. ( g ) Cell viability analysis of SOCS3-silenced and overexpressing cell lines. ( h ) Protein expression profiles in SOCS3-knockdown and overexpression models. ( i ) Absolute quantitative PCR analysis of PCV2 viral copy numbers in wild-type PK-15, si-NC, and si-SOCS3-2 cells infected with PCV2 (MOI = 1) at indicated time points. ( j ) PCV2 viral load quantification in wild-type PK-15, PK-15-pCDH, and PK-15-SOCS3 cells post-infection. ( k ) Indirect immunofluorescence detection of PCV2 infection status across experimental groups. Data are presented as mean ± SD ( n = 3). *** p < 0.001 vs. control.

    Journal: Viruses

    Article Title: PCV2 Infection Upregulates SOCS3 Expression to Facilitate Viral Replication in PK-15 Cells

    doi: 10.3390/v17081081

    Figure Lengend Snippet: SOCS3 expression facilitates PCV2 replication. ( a ) Fluorescence imaging of PK-15 cells transfected with varying concentrations of Cy3-labeled siRNA. ( b ) SOCS3 mRNA expression levels and ( c ) corresponding knockdown efficiency at different time points post-siRNA transfection. ( d ) Fluorescence visualization of HEK-293T cells at distinct time intervals following lentiviral vector transduction. ( e ) Fluorescence patterns of SOCS3-stably transfected cells and blank controls after 10 consecutive passages. ( f ) Relative SOCS3 mRNA expression levels in stably transfected cells. ( g ) Cell viability analysis of SOCS3-silenced and overexpressing cell lines. ( h ) Protein expression profiles in SOCS3-knockdown and overexpression models. ( i ) Absolute quantitative PCR analysis of PCV2 viral copy numbers in wild-type PK-15, si-NC, and si-SOCS3-2 cells infected with PCV2 (MOI = 1) at indicated time points. ( j ) PCV2 viral load quantification in wild-type PK-15, PK-15-pCDH, and PK-15-SOCS3 cells post-infection. ( k ) Indirect immunofluorescence detection of PCV2 infection status across experimental groups. Data are presented as mean ± SD ( n = 3). *** p < 0.001 vs. control.

    Article Snippet: Immunoblotting was performed using a rabbit polyclonal anti-SOCS3 antibody (Proteintech; 1:1000 dilution) incubated overnight at 4 °C, followed by incubation with a HRP-conjugated goat anti-rabbit secondary antibody (Servicebio; 1:3000 dilution) for 1 h at room temperature.

    Techniques: Expressing, Fluorescence, Imaging, Transfection, Labeling, Knockdown, Plasmid Preparation, Transduction, Stable Transfection, Over Expression, Real-time Polymerase Chain Reaction, Infection, Immunofluorescence, Control

    Effects of SOCS3 on PCV2-induced IFN-β and TNF-α mRNA expressions. ( a ) SOCS3 silencing suppresses IFN-β production in PCV2-infected host cells while ( b ) enhancing TNF-α expression. Relative quantitative PCR analysis of IFN-β and TNF-α mRNA levels in wild-type PK-15, si-NC, and si-SOCS3-2 cells infected with PCV2 (MOI = 1) at indicated time points. ( c ) SOCS3 overexpression promotes IFN-β production in PCV2-infected host cells, whereas ( d ) it inhibits TNF-α expression. Relative quantitative PCR analysis of IFN-β and TNF-α mRNA levels in wild-type PK-15, PK-15-pCDH, and PK-15-SOCS3 cells post-PCV2 infection (MOI = 1). Data are presented as mean ± SD ( n = 3). ** p < 0.01, *** p < 0.001 vs. control.

    Journal: Viruses

    Article Title: PCV2 Infection Upregulates SOCS3 Expression to Facilitate Viral Replication in PK-15 Cells

    doi: 10.3390/v17081081

    Figure Lengend Snippet: Effects of SOCS3 on PCV2-induced IFN-β and TNF-α mRNA expressions. ( a ) SOCS3 silencing suppresses IFN-β production in PCV2-infected host cells while ( b ) enhancing TNF-α expression. Relative quantitative PCR analysis of IFN-β and TNF-α mRNA levels in wild-type PK-15, si-NC, and si-SOCS3-2 cells infected with PCV2 (MOI = 1) at indicated time points. ( c ) SOCS3 overexpression promotes IFN-β production in PCV2-infected host cells, whereas ( d ) it inhibits TNF-α expression. Relative quantitative PCR analysis of IFN-β and TNF-α mRNA levels in wild-type PK-15, PK-15-pCDH, and PK-15-SOCS3 cells post-PCV2 infection (MOI = 1). Data are presented as mean ± SD ( n = 3). ** p < 0.01, *** p < 0.001 vs. control.

    Article Snippet: Immunoblotting was performed using a rabbit polyclonal anti-SOCS3 antibody (Proteintech; 1:1000 dilution) incubated overnight at 4 °C, followed by incubation with a HRP-conjugated goat anti-rabbit secondary antibody (Servicebio; 1:3000 dilution) for 1 h at room temperature.

    Techniques: Infection, Expressing, Real-time Polymerase Chain Reaction, Over Expression, Control

    The primary and secondary antibodies used in western blot assay

    Journal: Neural Regeneration Research

    Article Title: Heat shock factor 1 promotes neurite outgrowth and suppresses inflammation in the severed spinal cord of geckos

    doi: 10.4103/1673-5374.366495

    Figure Lengend Snippet: The primary and secondary antibodies used in western blot assay

    Article Snippet: Polyclonal rabbit anti-gecko SOCS3 antibody* , , , , GenScript Biotech Corp , WB.

    Techniques: Western Blot

    IL-6 production by cDC1 and cDC2 regulates differential IDO1 expression (A) Gene expression microarray analysis of cDC1 and cDC2 untreated or treated with LPS (250 ng/mL) for 24 h. Bright blue (lowest) to bright red (highest). (B) Heatmap of cytokines in supernatants from cDC1 and cDC2 cultures treated as (A) (n = 2). (C) IL-6-fold induction in LPS (250 ng/mL) stimulated cDC1 and cDC2 over the untreated control (n = 3). (D) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 3). (E) SOCS3 immunoblot in cDC1 and cDC2 treated as depicted for 24 h (n = 3). (F) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 4). (G) Analysis of skin reactivity is presented as change in footpad weight. n = 6 mice per group (n = 2). (H) EAE score of mixed bone marrow chimeras with bone marrow of indicated genotypes. 6 mice per group, n = 2. Data are shown as means ± SD. ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, two-way ANOVA followed by Bonferroni multiple comparison test (C and H) or Tukey’s multiple comparison test (G). β-Actin used as loading control (D–F). Please also see <xref ref-type=Figure S4 . " width="100%" height="100%">

    Journal: Immunity

    Article Title: Indoleamine 2,3-dioxygenase 1 activation in mature cDC1 promotes tolerogenic education of inflammatory cDC2 via metabolic communication

    doi: 10.1016/j.immuni.2022.05.013

    Figure Lengend Snippet: IL-6 production by cDC1 and cDC2 regulates differential IDO1 expression (A) Gene expression microarray analysis of cDC1 and cDC2 untreated or treated with LPS (250 ng/mL) for 24 h. Bright blue (lowest) to bright red (highest). (B) Heatmap of cytokines in supernatants from cDC1 and cDC2 cultures treated as (A) (n = 2). (C) IL-6-fold induction in LPS (250 ng/mL) stimulated cDC1 and cDC2 over the untreated control (n = 3). (D) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 3). (E) SOCS3 immunoblot in cDC1 and cDC2 treated as depicted for 24 h (n = 3). (F) IDO1 immunoblot in cDC1 and cDC2 treated as depicted for 48 h (n = 4). (G) Analysis of skin reactivity is presented as change in footpad weight. n = 6 mice per group (n = 2). (H) EAE score of mixed bone marrow chimeras with bone marrow of indicated genotypes. 6 mice per group, n = 2. Data are shown as means ± SD. ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, two-way ANOVA followed by Bonferroni multiple comparison test (C and H) or Tukey’s multiple comparison test (G). β-Actin used as loading control (D–F). Please also see Figure S4 .

    Article Snippet: Polyclonal rabbit anti-mouse SOCS3 , Cell Signaling , Cat#: 2923; RRID: AB_2255132.

    Techniques: Expressing, Gene Expression, Microarray, Control, Western Blot, Comparison

    Journal: Immunity

    Article Title: Indoleamine 2,3-dioxygenase 1 activation in mature cDC1 promotes tolerogenic education of inflammatory cDC2 via metabolic communication

    doi: 10.1016/j.immuni.2022.05.013

    Figure Lengend Snippet:

    Article Snippet: Polyclonal rabbit anti-mouse SOCS3 , Cell Signaling , Cat#: 2923; RRID: AB_2255132.

    Techniques: Produced, Virus, Subcloning, Recombinant, Electron Microscopy, Protease Inhibitor, Purification, Adjuvant, Modification, Selection, Western Blot, In Situ, Enzyme-linked Immunosorbent Assay, Reverse Transcription, SYBR Green Assay, Bradford Protein Assay, Control, Retroviral, Mouse Assay, Sequencing, Real-time Polymerase Chain Reaction, Cloning, Software