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primary rabbit polyclonal antibody against trpm8  (Danaher Inc)


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    Structured Review

    Danaher Inc primary rabbit polyclonal antibody against trpm8
    (A) <t>TRPM8</t> mRNA expression by semi-quantitative PCR in superior mesenteric artery with endothelium removed (n = 3). C, control; P1, 1 μL prostate RT reaction; P2, 2 μL prostate RT reaction, Me, 2 μL mesenteric artery RT reaction. (B) Western blot analysis of TRPM8 protein expression in rat vascular tissue. Molecular weight of TRPM8 was 125 KDa. Bottom panel: β actin used to demonstrate protein loading (at 42kDa).
    Primary Rabbit Polyclonal Antibody Against Trpm8, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 20243 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+rabbit+polyclonal+antibody+against+trpm8/Rabbit+Polyclonal+Anti-JAK2+(phospho+Y1007)+antibody/pmc04657920-50-30-38
    Average 99 stars, based on 20243 article reviews
    primary rabbit polyclonal antibody against trpm8 - by Bioz Stars, 2026-10
    99/100 stars

    Images

    1) Product Images from "TRPM8 Channel Activation Induced by Monoterpenoid Rotundifolone Underlies Mesenteric Artery Relaxation"

    Article Title: TRPM8 Channel Activation Induced by Monoterpenoid Rotundifolone Underlies Mesenteric Artery Relaxation

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0143171

    (A) TRPM8 mRNA expression by semi-quantitative PCR in superior mesenteric artery with endothelium removed (n = 3). C, control; P1, 1 μL prostate RT reaction; P2, 2 μL prostate RT reaction, Me, 2 μL mesenteric artery RT reaction. (B) Western blot analysis of TRPM8 protein expression in rat vascular tissue. Molecular weight of TRPM8 was 125 KDa. Bottom panel: β actin used to demonstrate protein loading (at 42kDa).
    Figure Legend Snippet: (A) TRPM8 mRNA expression by semi-quantitative PCR in superior mesenteric artery with endothelium removed (n = 3). C, control; P1, 1 μL prostate RT reaction; P2, 2 μL prostate RT reaction, Me, 2 μL mesenteric artery RT reaction. (B) Western blot analysis of TRPM8 protein expression in rat vascular tissue. Molecular weight of TRPM8 was 125 KDa. Bottom panel: β actin used to demonstrate protein loading (at 42kDa).

    Techniques Used: Expressing, Real-time Polymerase Chain Reaction, Western Blot, Molecular Weight

    Related Articles

    Membrane:

    Article Title: TRPM8 Channel Activation Induced by Monoterpenoid Rotundifolone Underlies Mesenteric Artery Relaxation
    Article Snippet: The protein samples were denatured and separated on a denaturing SDS/7.5% polyacrylamide gel, then transferred to a nitrocellulose membrane (PerkinElmer Inc, Waltham, Massachusetts, USA). .. The membrane was blocked with 5% (wt/vol) milk in TBS containing 0.1% Tween 20 (TBST) for 1 h at room temperature, followed by overnight incubation at 4°C with the specific primary rabbit polyclonal antibody against TRPM8 (1:1000 dilution; Abcam, Cambridge, Massachusetts, United States). .. After washing, the membrane was incubated with peroxidase-conjugated goat-anti-rabbit secondary antibody (1:3000 dilution; Abcam, Cambridge, Massachusetts, United States) at room temperature for 2 h. Protein loading was confirmed and normalized by comparing to β-actin levels.

    Incubation:

    Article Title: TRPM8 Channel Activation Induced by Monoterpenoid Rotundifolone Underlies Mesenteric Artery Relaxation
    Article Snippet: The protein samples were denatured and separated on a denaturing SDS/7.5% polyacrylamide gel, then transferred to a nitrocellulose membrane (PerkinElmer Inc, Waltham, Massachusetts, USA). .. The membrane was blocked with 5% (wt/vol) milk in TBS containing 0.1% Tween 20 (TBST) for 1 h at room temperature, followed by overnight incubation at 4°C with the specific primary rabbit polyclonal antibody against TRPM8 (1:1000 dilution; Abcam, Cambridge, Massachusetts, United States). .. After washing, the membrane was incubated with peroxidase-conjugated goat-anti-rabbit secondary antibody (1:3000 dilution; Abcam, Cambridge, Massachusetts, United States) at room temperature for 2 h. Protein loading was confirmed and normalized by comparing to β-actin levels.



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    primary rabbit polyclonal antibody against trpm8  (Danaher Inc)
    99
    Danaher Inc primary rabbit polyclonal antibody against trpm8
    (A) <t>TRPM8</t> mRNA expression by semi-quantitative PCR in superior mesenteric artery with endothelium removed (n = 3). C, control; P1, 1 μL prostate RT reaction; P2, 2 μL prostate RT reaction, Me, 2 μL mesenteric artery RT reaction. (B) Western blot analysis of TRPM8 protein expression in rat vascular tissue. Molecular weight of TRPM8 was 125 KDa. Bottom panel: β actin used to demonstrate protein loading (at 42kDa).
    Primary Rabbit Polyclonal Antibody Against Trpm8, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+rabbit+polyclonal+antibody+against+trpm8/Rabbit+Polyclonal+Anti-JAK2+(phospho+Y1007)+antibody/pmc04657920-50-30-38
    Average 99 stars, based on 1 article reviews
    primary rabbit polyclonal antibody against trpm8 - by Bioz Stars, 2026-10
    99/100 stars
    		  Buy from Supplier

    Image Search Results


    (A) TRPM8 mRNA expression by semi-quantitative PCR in superior mesenteric artery with endothelium removed (n = 3). C, control; P1, 1 μL prostate RT reaction; P2, 2 μL prostate RT reaction, Me, 2 μL mesenteric artery RT reaction. (B) Western blot analysis of TRPM8 protein expression in rat vascular tissue. Molecular weight of TRPM8 was 125 KDa. Bottom panel: β actin used to demonstrate protein loading (at 42kDa).

    Journal: PLoS ONE

    Article Title: TRPM8 Channel Activation Induced by Monoterpenoid Rotundifolone Underlies Mesenteric Artery Relaxation

    doi: 10.1371/journal.pone.0143171

    Figure Lengend Snippet: (A) TRPM8 mRNA expression by semi-quantitative PCR in superior mesenteric artery with endothelium removed (n = 3). C, control; P1, 1 μL prostate RT reaction; P2, 2 μL prostate RT reaction, Me, 2 μL mesenteric artery RT reaction. (B) Western blot analysis of TRPM8 protein expression in rat vascular tissue. Molecular weight of TRPM8 was 125 KDa. Bottom panel: β actin used to demonstrate protein loading (at 42kDa).

    Article Snippet: The membrane was blocked with 5% (wt/vol) milk in TBS containing 0.1% Tween 20 (TBST) for 1 h at room temperature, followed by overnight incubation at 4°C with the specific primary rabbit polyclonal antibody against TRPM8 (1:1000 dilution; Abcam, Cambridge, Massachusetts, United States).

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot, Molecular Weight