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anti prot α rabbit polyclonal antibody  (St Johns Laboratory)


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    Structured Review

    St Johns Laboratory anti prot α rabbit polyclonal antibody
    ATP-induced Bcl-2 and <t>ProT-α</t> expression, was attenuated in the presence of either PPADS or DHTS. Total cell extracts from Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS (non-selective P2R antagonist) or DHTS (HuR inhibitor) before stimulation with ATP for 48 h were subjected to western blot analysis and probed with either anti-Bcl-2 antibody ( A ) or anti-ProT-α antibody ( B ) or anti-β-actin antibody. The left lower panel shows a densitometric analysis of Bcl-2 in relation to β-actin level. C ProT-α expression in Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS or DHTS before stimulation with ATP for 48 h was measured using ELISA. Data represent means ± S.D. (n = 3), *** Significantly different from control at p < 0.001, and. ### Significantly different from ATP-treated cells at p < 0.001
    Anti Prot α Rabbit Polyclonal Antibody, supplied by St Johns Laboratory, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti prot α rabbit polyclonal antibody/product/St Johns Laboratory
    Average 92 stars, based on 2 article reviews
    anti prot α rabbit polyclonal antibody - by Bioz Stars, 2026-03
    92/100 stars

    Images

    1) Product Images from "Molecular mechanisms of extracellular-ATP-mediated colorectal cancer progression: Implication of purinergic receptors-mediated nucleocytoplasmic shuttling of HuR"

    Article Title: Molecular mechanisms of extracellular-ATP-mediated colorectal cancer progression: Implication of purinergic receptors-mediated nucleocytoplasmic shuttling of HuR

    Journal: Purinergic Signalling

    doi: 10.1007/s11302-024-10021-2

    ATP-induced Bcl-2 and ProT-α expression, was attenuated in the presence of either PPADS or DHTS. Total cell extracts from Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS (non-selective P2R antagonist) or DHTS (HuR inhibitor) before stimulation with ATP for 48 h were subjected to western blot analysis and probed with either anti-Bcl-2 antibody ( A ) or anti-ProT-α antibody ( B ) or anti-β-actin antibody. The left lower panel shows a densitometric analysis of Bcl-2 in relation to β-actin level. C ProT-α expression in Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS or DHTS before stimulation with ATP for 48 h was measured using ELISA. Data represent means ± S.D. (n = 3), *** Significantly different from control at p < 0.001, and. ### Significantly different from ATP-treated cells at p < 0.001
    Figure Legend Snippet: ATP-induced Bcl-2 and ProT-α expression, was attenuated in the presence of either PPADS or DHTS. Total cell extracts from Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS (non-selective P2R antagonist) or DHTS (HuR inhibitor) before stimulation with ATP for 48 h were subjected to western blot analysis and probed with either anti-Bcl-2 antibody ( A ) or anti-ProT-α antibody ( B ) or anti-β-actin antibody. The left lower panel shows a densitometric analysis of Bcl-2 in relation to β-actin level. C ProT-α expression in Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS or DHTS before stimulation with ATP for 48 h was measured using ELISA. Data represent means ± S.D. (n = 3), *** Significantly different from control at p < 0.001, and. ### Significantly different from ATP-treated cells at p < 0.001

    Techniques Used: Expressing, Control, Western Blot, Enzyme-linked Immunosorbent Assay



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    anti prot α rabbit polyclonal antibody  (St Johns Laboratory)
    92
    St Johns Laboratory anti prot α rabbit polyclonal antibody
    ATP-induced Bcl-2 and <t>ProT-α</t> expression, was attenuated in the presence of either PPADS or DHTS. Total cell extracts from Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS (non-selective P2R antagonist) or DHTS (HuR inhibitor) before stimulation with ATP for 48 h were subjected to western blot analysis and probed with either anti-Bcl-2 antibody ( A ) or anti-ProT-α antibody ( B ) or anti-β-actin antibody. The left lower panel shows a densitometric analysis of Bcl-2 in relation to β-actin level. C ProT-α expression in Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS or DHTS before stimulation with ATP for 48 h was measured using ELISA. Data represent means ± S.D. (n = 3), *** Significantly different from control at p < 0.001, and. ### Significantly different from ATP-treated cells at p < 0.001
    Anti Prot α Rabbit Polyclonal Antibody, supplied by St Johns Laboratory, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti prot α rabbit polyclonal antibody/product/St Johns Laboratory
    Average 92 stars, based on 1 article reviews
    anti prot α rabbit polyclonal antibody - by Bioz Stars, 2026-03
    92/100 stars
    		  Buy from Supplier

    Image Search Results


    ATP-induced Bcl-2 and ProT-α expression, was attenuated in the presence of either PPADS or DHTS. Total cell extracts from Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS (non-selective P2R antagonist) or DHTS (HuR inhibitor) before stimulation with ATP for 48 h were subjected to western blot analysis and probed with either anti-Bcl-2 antibody ( A ) or anti-ProT-α antibody ( B ) or anti-β-actin antibody. The left lower panel shows a densitometric analysis of Bcl-2 in relation to β-actin level. C ProT-α expression in Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS or DHTS before stimulation with ATP for 48 h was measured using ELISA. Data represent means ± S.D. (n = 3), *** Significantly different from control at p < 0.001, and. ### Significantly different from ATP-treated cells at p < 0.001

    Journal: Purinergic Signalling

    Article Title: Molecular mechanisms of extracellular-ATP-mediated colorectal cancer progression: Implication of purinergic receptors-mediated nucleocytoplasmic shuttling of HuR

    doi: 10.1007/s11302-024-10021-2

    Figure Lengend Snippet: ATP-induced Bcl-2 and ProT-α expression, was attenuated in the presence of either PPADS or DHTS. Total cell extracts from Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS (non-selective P2R antagonist) or DHTS (HuR inhibitor) before stimulation with ATP for 48 h were subjected to western blot analysis and probed with either anti-Bcl-2 antibody ( A ) or anti-ProT-α antibody ( B ) or anti-β-actin antibody. The left lower panel shows a densitometric analysis of Bcl-2 in relation to β-actin level. C ProT-α expression in Caco-2 cells treated with either vehicle (Control) or ATP (100 μM) or pretreated for 60 min with PPADS or DHTS before stimulation with ATP for 48 h was measured using ELISA. Data represent means ± S.D. (n = 3), *** Significantly different from control at p < 0.001, and. ### Significantly different from ATP-treated cells at p < 0.001

    Article Snippet: Anti-Bcl-2 rabbit polyclonal antibody, anti-HIF1-α rabbit polyclonal antibody, anti-ProT-α rabbit polyclonal antibody and anti-VEGF-A rabbit polyclonal antibody were obtained from St John’s Laboratory Ltd (UK). β-actin monoclonal antibody was obtained from Cell Signaling Technology (USA).

    Techniques: Expressing, Control, Western Blot, Enzyme-linked Immunosorbent Assay