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hsp27 g31 mab  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc hsp27 g31 mab
    The primary antibodies used for immunohistochemistry and Western blot analysis.
    Hsp27 G31 Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 218 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/g31/HSP27+Mouse+mAb/pmc10377083-19-2-12
    Average 95 stars, based on 218 article reviews
    hsp27 g31 mab - by Bioz Stars, 2026-09
    95/100 stars

    Images

    1) Product Images from "Pro-Calcifying Role of Enzymatically Modified LDL (eLDL) in Aortic Valve Sclerosis via Induction of IL-6 and IL-33"

    Article Title: Pro-Calcifying Role of Enzymatically Modified LDL (eLDL) in Aortic Valve Sclerosis via Induction of IL-6 and IL-33

    Journal: Biomolecules

    doi: 10.3390/biom13071091

    The primary antibodies used for immunohistochemistry and Western blot analysis.
    Figure Legend Snippet: The primary antibodies used for immunohistochemistry and Western blot analysis.

    Techniques Used: Immunohistochemistry, Western Blot

    p38 MAPK and eLDL in human aortic valves. ( A ) Detection of rapidly phosphorylated p38 MAPK upon treatment of VICs/myofibroblasts with eLDL. Cells were exposed to 10 or 20 µg/mL eLDL for 30 min. Cells without treatment served as control. Phosphorylated p38 MAPK and total p38 MAPK in whole-cell lysates were sequentially detected by Western blot analysis on the same membrane. Blots were re-probed with β-actin antibody to confirm equal loading. ( B ) WB quantification of the phosphorylation of p38 MAPK. ( C ) Expression of p38 MAPK isoforms in VICs/myofibroblasts. Relative mRNA levels for p38 subtypes quantified in VICs/myofibroblasts from 10 different patients using real-time PCR. Expression levels are given as RQ of target genes (p38α/MAPK14, p38β/MAPK11, p38γ/MAPK12, p38δ/MAPK13) normalized to the reference gene GAPDH. ( D ) Representative immunohistochemical staining of aortic valves sections stained with ( a ), anti-p38; ( b ), anti-phospho-p38; ( c ), anti-Hsp27; ( d ), anti-phospho-Hsp27. The fibrosa with the aortic side of the valve is on top.
    Figure Legend Snippet: p38 MAPK and eLDL in human aortic valves. ( A ) Detection of rapidly phosphorylated p38 MAPK upon treatment of VICs/myofibroblasts with eLDL. Cells were exposed to 10 or 20 µg/mL eLDL for 30 min. Cells without treatment served as control. Phosphorylated p38 MAPK and total p38 MAPK in whole-cell lysates were sequentially detected by Western blot analysis on the same membrane. Blots were re-probed with β-actin antibody to confirm equal loading. ( B ) WB quantification of the phosphorylation of p38 MAPK. ( C ) Expression of p38 MAPK isoforms in VICs/myofibroblasts. Relative mRNA levels for p38 subtypes quantified in VICs/myofibroblasts from 10 different patients using real-time PCR. Expression levels are given as RQ of target genes (p38α/MAPK14, p38β/MAPK11, p38γ/MAPK12, p38δ/MAPK13) normalized to the reference gene GAPDH. ( D ) Representative immunohistochemical staining of aortic valves sections stained with ( a ), anti-p38; ( b ), anti-phospho-p38; ( c ), anti-Hsp27; ( d ), anti-phospho-Hsp27. The fibrosa with the aortic side of the valve is on top.

    Techniques Used: Control, Western Blot, Membrane, Phospho-proteomics, Expressing, Real-time Polymerase Chain Reaction, Immunohistochemical staining, Staining

    Related Articles

    Phospho-proteomics:

    Article Title: Noninvasive Physical Plasma as Innovative and Tissue-Preserving Therapy for Women Positive for Cervical Intraepithelial Neoplasia
    Article Snippet: .. The following primary antibodies were used: pH 3-specific antibody: 9701, Cell Signaling Technology(Danvers, MA, USA), 1:200; Cyclin B1-specific antibody: ab32053 (Y160), Abcam, 1:200; protein kinase B (pAKT)-specific antibody: 12,178 (D5G4), Cell Signaling Technology, 1:200; heat shock protein 27 (HSP27)-specific antibody: 2402 (G31), Cell Signaling Technology, 1:200; Bcl2-family member Bim (Bim)-specific antibody: 2819, Cell Signaling Technology, 1:200; Caspase 9 (Casp9)-specific antibody: 9502, Cell Signaling Technology, 1:200; p53 phosphorylation (pp53)-specific antibody: 9284, Cell Signaling Technology, 1:200; p53 binding protein 1 (53BP1)-specific antibody: 4937, Cell Signaling Technology, 1:200. ..

    Binding Assay:

    Article Title: Noninvasive Physical Plasma as Innovative and Tissue-Preserving Therapy for Women Positive for Cervical Intraepithelial Neoplasia
    Article Snippet: .. The following primary antibodies were used: pH 3-specific antibody: 9701, Cell Signaling Technology(Danvers, MA, USA), 1:200; Cyclin B1-specific antibody: ab32053 (Y160), Abcam, 1:200; protein kinase B (pAKT)-specific antibody: 12,178 (D5G4), Cell Signaling Technology, 1:200; heat shock protein 27 (HSP27)-specific antibody: 2402 (G31), Cell Signaling Technology, 1:200; Bcl2-family member Bim (Bim)-specific antibody: 2819, Cell Signaling Technology, 1:200; Caspase 9 (Casp9)-specific antibody: 9502, Cell Signaling Technology, 1:200; p53 phosphorylation (pp53)-specific antibody: 9284, Cell Signaling Technology, 1:200; p53 binding protein 1 (53BP1)-specific antibody: 4937, Cell Signaling Technology, 1:200. ..



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    Image Search Results


    The primary antibodies used for immunohistochemistry and Western blot analysis.

    Journal: Biomolecules

    Article Title: Pro-Calcifying Role of Enzymatically Modified LDL (eLDL) in Aortic Valve Sclerosis via Induction of IL-6 and IL-33

    doi: 10.3390/biom13071091

    Figure Lengend Snippet: The primary antibodies used for immunohistochemistry and Western blot analysis.

    Article Snippet: Hsp27 , HSP27 (G31) mAb , IHC-P , 1:200 , Mouse , Cell Signaling Technology.

    Techniques: Immunohistochemistry, Western Blot

    p38 MAPK and eLDL in human aortic valves. ( A ) Detection of rapidly phosphorylated p38 MAPK upon treatment of VICs/myofibroblasts with eLDL. Cells were exposed to 10 or 20 µg/mL eLDL for 30 min. Cells without treatment served as control. Phosphorylated p38 MAPK and total p38 MAPK in whole-cell lysates were sequentially detected by Western blot analysis on the same membrane. Blots were re-probed with β-actin antibody to confirm equal loading. ( B ) WB quantification of the phosphorylation of p38 MAPK. ( C ) Expression of p38 MAPK isoforms in VICs/myofibroblasts. Relative mRNA levels for p38 subtypes quantified in VICs/myofibroblasts from 10 different patients using real-time PCR. Expression levels are given as RQ of target genes (p38α/MAPK14, p38β/MAPK11, p38γ/MAPK12, p38δ/MAPK13) normalized to the reference gene GAPDH. ( D ) Representative immunohistochemical staining of aortic valves sections stained with ( a ), anti-p38; ( b ), anti-phospho-p38; ( c ), anti-Hsp27; ( d ), anti-phospho-Hsp27. The fibrosa with the aortic side of the valve is on top.

    Journal: Biomolecules

    Article Title: Pro-Calcifying Role of Enzymatically Modified LDL (eLDL) in Aortic Valve Sclerosis via Induction of IL-6 and IL-33

    doi: 10.3390/biom13071091

    Figure Lengend Snippet: p38 MAPK and eLDL in human aortic valves. ( A ) Detection of rapidly phosphorylated p38 MAPK upon treatment of VICs/myofibroblasts with eLDL. Cells were exposed to 10 or 20 µg/mL eLDL for 30 min. Cells without treatment served as control. Phosphorylated p38 MAPK and total p38 MAPK in whole-cell lysates were sequentially detected by Western blot analysis on the same membrane. Blots were re-probed with β-actin antibody to confirm equal loading. ( B ) WB quantification of the phosphorylation of p38 MAPK. ( C ) Expression of p38 MAPK isoforms in VICs/myofibroblasts. Relative mRNA levels for p38 subtypes quantified in VICs/myofibroblasts from 10 different patients using real-time PCR. Expression levels are given as RQ of target genes (p38α/MAPK14, p38β/MAPK11, p38γ/MAPK12, p38δ/MAPK13) normalized to the reference gene GAPDH. ( D ) Representative immunohistochemical staining of aortic valves sections stained with ( a ), anti-p38; ( b ), anti-phospho-p38; ( c ), anti-Hsp27; ( d ), anti-phospho-Hsp27. The fibrosa with the aortic side of the valve is on top.

    Article Snippet: Hsp27 , HSP27 (G31) mAb , IHC-P , 1:200 , Mouse , Cell Signaling Technology.

    Techniques: Control, Western Blot, Membrane, Phospho-proteomics, Expressing, Real-time Polymerase Chain Reaction, Immunohistochemical staining, Staining

    Optical micrographs of a cross-section of the entire fixed finger of the claw after polishing and the hardness at four characteristic areas were obtained via Vickers tests. The tests were performed more than five times for each site, and the site is 100–200 μm away from the outer and inner surfaces. Here, den(S) and den(M) denote small and medium denticles, and den(L1) and den(L2) denote large denticles .

    Journal: Materials

    Article Title: Mechanical Resistance and Tissue Structure of Claw Denticles of Various Sizes in the Mud Crab, Scylla serrata

    doi: 10.3390/ma16114114

    Figure Lengend Snippet: Optical micrographs of a cross-section of the entire fixed finger of the claw after polishing and the hardness at four characteristic areas were obtained via Vickers tests. The tests were performed more than five times for each site, and the site is 100–200 μm away from the outer and inner surfaces. Here, den(S) and den(M) denote small and medium denticles, and den(L1) and den(L2) denote large denticles .

    Article Snippet: The Vickers and nanoindentation tests were conducted using a Shimadzu Micro Vickers Hardness Tester, HMV-G31 (SHIMADZU, Kyoto, Japan), and an ENT-NEXUS (ELIONIX, Tokyo, Japan).

    Techniques: