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rabbit polyclonal antibody against pig ppar γ  (Bio-Rad)


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    Structured Review

    Bio-Rad rabbit polyclonal antibody against pig ppar γ
    Immunohistochemical staining for peroxisome proliferator-activated receptor gamma <t>(PPAR-γ)</t> expression in the vascular smooth muscle cells (VSMCs) in each group. The immunohistochemical staining was conducted 90 days after stenting. A: Normal control group, B: Stenting group, C: Stenting plus rosiglitazone (ROSI) treatment group. PPAR-γ-positive VSMCs are shown by their nuclear brown staining (×100).
    Rabbit Polyclonal Antibody Against Pig Ppar γ, supplied by Bio-Rad, 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/product/rabbit+polyclonal+antibody+against+pig+ppar+%CE%B3/Rabbit+anti+Pig+Interferon+Gamma/pmc06965304-123-21-28
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal antibody against pig ppar γ - by Bioz Stars, 2026-09
    86/100 stars

    Images

    1) Product Images from "Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model"

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model

    Journal: International Journal of Clinical and Experimental Pathology

    doi:

    Immunohistochemical staining for peroxisome proliferator-activated receptor gamma (PPAR-γ) expression in the vascular smooth muscle cells (VSMCs) in each group. The immunohistochemical staining was conducted 90 days after stenting. A: Normal control group, B: Stenting group, C: Stenting plus rosiglitazone (ROSI) treatment group. PPAR-γ-positive VSMCs are shown by their nuclear brown staining (×100).
    Figure Legend Snippet: Immunohistochemical staining for peroxisome proliferator-activated receptor gamma (PPAR-γ) expression in the vascular smooth muscle cells (VSMCs) in each group. The immunohistochemical staining was conducted 90 days after stenting. A: Normal control group, B: Stenting group, C: Stenting plus rosiglitazone (ROSI) treatment group. PPAR-γ-positive VSMCs are shown by their nuclear brown staining (×100).

    Techniques Used: Immunohistochemical staining, Staining, Expressing, Control

    Western blot assay for the expression of minipig carotid artery peroxisome proliferator-activated receptor gamma (PPAR-γ) and smooth muscle 22-alpha (SM22α). The carotid artery tissues were harvested and the total protein was extracted for the western blot analysis by using anti-PPAR-γ, anti-SM22α, and anti-β-actin primary antibodies. The immunocomplexes were detected using horseradish peroxidase-conjugated secondary antibodies, followed by enhanced chemiluminescence. The relative molecular masses of the target proteins are indicated.
    Figure Legend Snippet: Western blot assay for the expression of minipig carotid artery peroxisome proliferator-activated receptor gamma (PPAR-γ) and smooth muscle 22-alpha (SM22α). The carotid artery tissues were harvested and the total protein was extracted for the western blot analysis by using anti-PPAR-γ, anti-SM22α, and anti-β-actin primary antibodies. The immunocomplexes were detected using horseradish peroxidase-conjugated secondary antibodies, followed by enhanced chemiluminescence. The relative molecular masses of the target proteins are indicated.

    Techniques Used: Western Blot, Expressing

    Related Articles

    Immunohistochemical staining:

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model
    Article Snippet: .. After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining. ..

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model
    Article Snippet: .. Immunohistochemistry and western blotting After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining. ..

    Staining:

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model
    Article Snippet: .. After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining. ..

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model
    Article Snippet: .. Immunohistochemistry and western blotting After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining. ..

    Immunohistochemistry:

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model
    Article Snippet: .. Immunohistochemistry and western blotting After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining. ..

    Western Blot:

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model
    Article Snippet: .. Immunohistochemistry and western blotting After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining. ..



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    Bio-Rad rabbit polyclonal antibody against pig ppar γ
    Immunohistochemical staining for peroxisome proliferator-activated receptor gamma <t>(PPAR-γ)</t> expression in the vascular smooth muscle cells (VSMCs) in each group. The immunohistochemical staining was conducted 90 days after stenting. A: Normal control group, B: Stenting group, C: Stenting plus rosiglitazone (ROSI) treatment group. PPAR-γ-positive VSMCs are shown by their nuclear brown staining (×100).
    Rabbit Polyclonal Antibody Against Pig Ppar γ, supplied by Bio-Rad, 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/product/rabbit+polyclonal+antibody+against+pig+ppar+%CE%B3/Rabbit+anti+Pig+Interferon+Gamma/pmc06965304-123-21-28
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal antibody against pig ppar γ - by Bioz Stars, 2026-09
    86/100 stars
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    Immunohistochemical staining for peroxisome proliferator-activated receptor gamma (PPAR-γ) expression in the vascular smooth muscle cells (VSMCs) in each group. The immunohistochemical staining was conducted 90 days after stenting. A: Normal control group, B: Stenting group, C: Stenting plus rosiglitazone (ROSI) treatment group. PPAR-γ-positive VSMCs are shown by their nuclear brown staining (×100).

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model

    doi:

    Figure Lengend Snippet: Immunohistochemical staining for peroxisome proliferator-activated receptor gamma (PPAR-γ) expression in the vascular smooth muscle cells (VSMCs) in each group. The immunohistochemical staining was conducted 90 days after stenting. A: Normal control group, B: Stenting group, C: Stenting plus rosiglitazone (ROSI) treatment group. PPAR-γ-positive VSMCs are shown by their nuclear brown staining (×100).

    Article Snippet: After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining.

    Techniques: Immunohistochemical staining, Staining, Expressing, Control

    Western blot assay for the expression of minipig carotid artery peroxisome proliferator-activated receptor gamma (PPAR-γ) and smooth muscle 22-alpha (SM22α). The carotid artery tissues were harvested and the total protein was extracted for the western blot analysis by using anti-PPAR-γ, anti-SM22α, and anti-β-actin primary antibodies. The immunocomplexes were detected using horseradish peroxidase-conjugated secondary antibodies, followed by enhanced chemiluminescence. The relative molecular masses of the target proteins are indicated.

    Journal: International Journal of Clinical and Experimental Pathology

    Article Title: Decreased PPAR-γ expression after internal carotid artery stenting is associated with vascular lesions induced by smooth muscle cell proliferation and systemic inflammation in a minipig model

    doi:

    Figure Lengend Snippet: Western blot assay for the expression of minipig carotid artery peroxisome proliferator-activated receptor gamma (PPAR-γ) and smooth muscle 22-alpha (SM22α). The carotid artery tissues were harvested and the total protein was extracted for the western blot analysis by using anti-PPAR-γ, anti-SM22α, and anti-β-actin primary antibodies. The immunocomplexes were detected using horseradish peroxidase-conjugated secondary antibodies, followed by enhanced chemiluminescence. The relative molecular masses of the target proteins are indicated.

    Article Snippet: After deparaffinization and hydration, the specimens were blocked with 0.3% H 2 O 2 at room temperature for 15 min. A rabbit polyclonal antibody against pig-PPAR-γ (2.5 μg/ml, ABD Serotec, USA) was used for immunohistochemical staining.

    Techniques: Western Blot, Expressing