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total bax  (Bio-Techne corporation)


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    Structured Review

    Bio-Techne corporation total bax
    Total Bax, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/total+bax/Bax+Antibody/pm34762220-55-20-22
    Average 94 stars, based on 10 article reviews
    total bax - by Bioz Stars, 2026-09
    94/100 stars

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    Article Title: Nucleophosmin, a Critical Bax Cofactor in Ischemia-Induced Cell Death
    Article Snippet: Antibodies directed against NPM, β-actin, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH; Sigma-Aldrich, St. Louis, MO), conformationally changed (i.e., 6A7 epitope-exposed) Bax and total Bax (Trevigen, Gaithersburg, MD), F 1 F 0 ATPase (complex V β subunit; Invitrogen, Carlsbad, CA), and cytochrome c and caspase 3 (Clontech, Mountain View, CA) were purchased from commercial sources.

    Article Title: Mechanisms of nucleophosmin (NPM)-mediated regulated cell death elucidated by Hsp70 during renal ischemia.
    Article Snippet: Nucleophosmin (NPM), a nucleolar-based protein chaperone, promotes Bax-mediated mitochondrial injury and regulates cell death during acute kidney injury.. However, the steps that transform NPM from an essential to a toxic protein during stress are unknown.. To localize NPM-mediated events causing regulated cell death during ischemia, wild type (WT) and Hsp70 mutant proteins with characterized intracellular trafficking defects that restrict movement to either the nucleolar region (M45) or cytosol (985A) were expressed in primary murine proximal tubule epithelial cells (PTEC) harvested from Hsp70 null mice.

    Article Title: Nucleophosmin, a Critical Bax Cofactor in Ischemia-Induced Cell Death
    Article Snippet: Antibodies directed against NPM, -actin, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH; Sigma-Aldrich, St. Louis, MO), conformationally changed (i.e., 6A7 epitope-exposed) Bax and total Bax (Trevigen, Gaithersburg, MD), F1F0 ATPase (complex V subunit; Invitrogen, Carlsbad, CA), and cytochrome c and caspase 3 (Clontech, Mountain View, CA) were purchased from commercial sources.



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    Flow cytometry analysis followed by Bax protein expression. H9c2 cells were transfected with pEGFP, pEGFP and pcDNA3-HA- HIF-1α or pcDNA3-Flag-DN-HIF-1α and were sorted in a flow cytometer. The EGFP positive sorted cells were subjected to hypoxia for 6 h. Total Bax expression in the same lysates was used to monitor protein loading. N = Normoxia; H = Hypoxia. The data are representative of 3 separate experiments and only 2 experiments using dominant negative Hif-1α (right panel).

    Journal: BMC Cardiovascular Disorders

    Article Title: Hypoxia-inducible factor-1alpha is a critical mediator of hypoxia induced apoptosis in cardiac H9c2 and kidney epithelial HK-2 cells

    doi: 10.1186/1471-2261-8-9

    Figure Lengend Snippet: Flow cytometry analysis followed by Bax protein expression. H9c2 cells were transfected with pEGFP, pEGFP and pcDNA3-HA- HIF-1α or pcDNA3-Flag-DN-HIF-1α and were sorted in a flow cytometer. The EGFP positive sorted cells were subjected to hypoxia for 6 h. Total Bax expression in the same lysates was used to monitor protein loading. N = Normoxia; H = Hypoxia. The data are representative of 3 separate experiments and only 2 experiments using dominant negative Hif-1α (right panel).

    Article Snippet: After blocking with TBS/5% skim milk, the membranes were incubated overnight at 4°C with primary antibodies against Hif-1α (1:500 dilution, Novus Biologicals, Littleton, CO), the active monomer of Bax (Monoclonal antibody 6A7, 0.5 μg/ml concentration, Alexis Biochemicals, San Diego, CA) or total Bax (1:1000 dilution, Santa Cruz Biotechnology, Santa Cruz, CA), followed by secondary antibodies conjugated with horseradish peroxidase (1:10,000) (Pierce, Rockford, IL) for 1 h at room temperature.

    Techniques: Flow Cytometry, Expressing, Transfection, Dominant Negative Mutation

    HIF-1α promotes Bax activation in HK-2 cells. Cells were subjected to normoxia or hypoxia of 16 h after sorting in a flow cytometer. Active and Total Bax protein expression of the whole cell lysates of EGFP positive cells is shown of cells transfected with either pEGFP or pEGFP and pcDNA3-HA-Hif-1α or pcDNA3-DN-Hif-1α. N = Normoxia; H = Hypoxia. Data shown is representative of two separate experiments.

    Journal: BMC Cardiovascular Disorders

    Article Title: Hypoxia-inducible factor-1alpha is a critical mediator of hypoxia induced apoptosis in cardiac H9c2 and kidney epithelial HK-2 cells

    doi: 10.1186/1471-2261-8-9

    Figure Lengend Snippet: HIF-1α promotes Bax activation in HK-2 cells. Cells were subjected to normoxia or hypoxia of 16 h after sorting in a flow cytometer. Active and Total Bax protein expression of the whole cell lysates of EGFP positive cells is shown of cells transfected with either pEGFP or pEGFP and pcDNA3-HA-Hif-1α or pcDNA3-DN-Hif-1α. N = Normoxia; H = Hypoxia. Data shown is representative of two separate experiments.

    Article Snippet: After blocking with TBS/5% skim milk, the membranes were incubated overnight at 4°C with primary antibodies against Hif-1α (1:500 dilution, Novus Biologicals, Littleton, CO), the active monomer of Bax (Monoclonal antibody 6A7, 0.5 μg/ml concentration, Alexis Biochemicals, San Diego, CA) or total Bax (1:1000 dilution, Santa Cruz Biotechnology, Santa Cruz, CA), followed by secondary antibodies conjugated with horseradish peroxidase (1:10,000) (Pierce, Rockford, IL) for 1 h at room temperature.

    Techniques: Activation Assay, Flow Cytometry, Expressing, Transfection

    ( A ) Immunoblot of active Bax ( upper panel ) detected with an anti-6A7 epitope-specific antibody in MFN2 f/f proximal tubule epithelial lysates of cells transduced with no virus ( NT ), empty adenovirus ( CTL ) or Cre adenovirus ( MFN2- ) at baseline and 30 min after ATP depletion; total Bax controls are show for sample loading (lower panel) ; and ( B ) densitometric analysis of the relative increase in active 6A7-Bax content after metabolic stress.

    Journal: PLoS ONE

    Article Title: Role of Mitofusin 2 in the Renal Stress Response

    doi: 10.1371/journal.pone.0031074

    Figure Lengend Snippet: ( A ) Immunoblot of active Bax ( upper panel ) detected with an anti-6A7 epitope-specific antibody in MFN2 f/f proximal tubule epithelial lysates of cells transduced with no virus ( NT ), empty adenovirus ( CTL ) or Cre adenovirus ( MFN2- ) at baseline and 30 min after ATP depletion; total Bax controls are show for sample loading (lower panel) ; and ( B ) densitometric analysis of the relative increase in active 6A7-Bax content after metabolic stress.

    Article Snippet: Total Bax antibody was purchased from Cell Signaling Technologies (Danvers, MA).

    Techniques: Western Blot, Transduction

    A) IEC-6 cells were treated with different concentrations of GLN (0, 2, 10, and 20 mM) with or without 1 h prior PD98059 treatment. Cell survival was measured via MTS assay. Results are shown as mean±SEM (n = 3). B) [T(P) 202 /Y(P) 204 ]ERK1/2 and total ERK1/2 levels were determined by Western blot analysis after basal and stressed 43°C conditions without recovery. ERK1/2 activation is shown as mean fold change relative to total ERK1/2±SEM and ratioed to 0 mM GLN (n = 3).

    Journal: PLoS ONE

    Article Title: Fibronectin-Integrin Signaling Is Required for L-Glutamine’s Protection against Gut Injury

    doi: 10.1371/journal.pone.0050185

    Figure Lengend Snippet: A) IEC-6 cells were treated with different concentrations of GLN (0, 2, 10, and 20 mM) with or without 1 h prior PD98059 treatment. Cell survival was measured via MTS assay. Results are shown as mean±SEM (n = 3). B) [T(P) 202 /Y(P) 204 ]ERK1/2 and total ERK1/2 levels were determined by Western blot analysis after basal and stressed 43°C conditions without recovery. ERK1/2 activation is shown as mean fold change relative to total ERK1/2±SEM and ratioed to 0 mM GLN (n = 3).

    Article Snippet: Primary antibodies against HSP32 and HSP70 (1∶10,000 dilution) (StressGen, Victoria, BC, Canada) and FN (1∶10,000), or against total ERK1/2, [T(P) 202 /Y(P) 204 ]ERK1/2, total HSF-1, [S(P) 303 ]HSF-1, cleaved caspase-3, cleaved PARP, bax, and bcl-2 (1∶1,000) (Cell signaling, Danvers, MA) were used.

    Techniques: MTS Assay, Western Blot, Activation Assay

    GLN is protective in the intestine by preventing FN degradation after thermal injury, as well as by activating the protective FN-Integrin signaling pathway. GLN phosphorylates ERK1/2 via the FN-Integrin pathway leading to HSF-1 activation, which enhances HSP expression to prevent apoptosis.

    Journal: PLoS ONE

    Article Title: Fibronectin-Integrin Signaling Is Required for L-Glutamine’s Protection against Gut Injury

    doi: 10.1371/journal.pone.0050185

    Figure Lengend Snippet: GLN is protective in the intestine by preventing FN degradation after thermal injury, as well as by activating the protective FN-Integrin signaling pathway. GLN phosphorylates ERK1/2 via the FN-Integrin pathway leading to HSF-1 activation, which enhances HSP expression to prevent apoptosis.

    Article Snippet: Primary antibodies against HSP32 and HSP70 (1∶10,000 dilution) (StressGen, Victoria, BC, Canada) and FN (1∶10,000), or against total ERK1/2, [T(P) 202 /Y(P) 204 ]ERK1/2, total HSF-1, [S(P) 303 ]HSF-1, cleaved caspase-3, cleaved PARP, bax, and bcl-2 (1∶1,000) (Cell signaling, Danvers, MA) were used.

    Techniques: Activation Assay, Expressing

    (A) MCF-7_shCON, MCF-7_shRab5A or MCF-7_shRab5C cells, treated with STS (4 hrs), or TNFα/AcD (6 hrs). IF of total cellular BAX (α-BAX N-20) and of BAX in active conformation (α-BAX 6A7).

    Journal: Developmental cell

    Article Title: Endolysosomal Targeting of Mitochondria is Integral to BAX-mediated Mitochondrial Permeabilization During Apoptosis Signaling

    doi: 10.1016/j.devcel.2020.05.014

    Figure Lengend Snippet: (A) MCF-7_shCON, MCF-7_shRab5A or MCF-7_shRab5C cells, treated with STS (4 hrs), or TNFα/AcD (6 hrs). IF of total cellular BAX (α-BAX N-20) and of BAX in active conformation (α-BAX 6A7).

    Article Snippet: Following, cells were incubated with a conformation-specific BAX antibody 6A7 (Abcam) and an antibody detecting total cellular BAX (Santa Cruz Biotechnology) at 37°C for 1 hr.

    Techniques: