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primary mouse monoclonal anti-pgk1  (Thermo Fisher)


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    Structured Review

    Thermo Fisher primary mouse monoclonal anti-pgk1
    Primary Mouse Monoclonal Anti Pgk1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+pgk1/anti+pgk1/pmc12222759-453-43-47
    Average 90 stars, based on 1 article reviews
    primary mouse monoclonal anti-pgk1 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Centrifugation:

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons.
    Article Snippet: Strains were grown to 0.8 OD600, followed by addition of cycloheximide (C4859, Sigma-Aldrich) to a final concentration of 100μg/ml to block protein synthesis. .. At each time point, ~8 × 107 cells were harvestedby centrifugation.Whole cell extracts wereprepared by alkaline lysis followed by precipitation with trichloroacetic acid95 and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Alkaline Lysis:

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons.
    Article Snippet: Strains were grown to 0.8 OD600, followed by addition of cycloheximide (C4859, Sigma-Aldrich) to a final concentration of 100μg/ml to block protein synthesis. .. At each time point, ~8 × 107 cells were harvestedby centrifugation.Whole cell extracts wereprepared by alkaline lysis followed by precipitation with trichloroacetic acid95 and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons
    Article Snippet: .. Whole cell extracts were prepared by alkaline lysis followed by precipitation with trichloroacetic acid and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (11814460001, Roche), mouse anti-Pgk1 (459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons
    Article Snippet: .. Whole cell extracts were prepared by alkaline lysis followed by precipitation with trichloroacetic acid and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Western Blot:

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons.
    Article Snippet: Strains were grown to 0.8 OD600, followed by addition of cycloheximide (C4859, Sigma-Aldrich) to a final concentration of 100μg/ml to block protein synthesis. .. At each time point, ~8 × 107 cells were harvestedby centrifugation.Whole cell extracts wereprepared by alkaline lysis followed by precipitation with trichloroacetic acid95 and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons
    Article Snippet: .. Whole cell extracts were prepared by alkaline lysis followed by precipitation with trichloroacetic acid and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (11814460001, Roche), mouse anti-Pgk1 (459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons
    Article Snippet: .. Whole cell extracts were prepared by alkaline lysis followed by precipitation with trichloroacetic acid and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Control:

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons.
    Article Snippet: Strains were grown to 0.8 OD600, followed by addition of cycloheximide (C4859, Sigma-Aldrich) to a final concentration of 100μg/ml to block protein synthesis. .. At each time point, ~8 × 107 cells were harvestedby centrifugation.Whole cell extracts wereprepared by alkaline lysis followed by precipitation with trichloroacetic acid95 and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons
    Article Snippet: .. Whole cell extracts were prepared by alkaline lysis followed by precipitation with trichloroacetic acid and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (11814460001, Roche), mouse anti-Pgk1 (459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Article Title: Orphan quality control by an SCF ubiquitin ligase directed to pervasive C-degrons
    Article Snippet: .. Whole cell extracts were prepared by alkaline lysis followed by precipitation with trichloroacetic acid and separated by SDS-PAGE, followed by immunoblotting against GFP and against the loading control Pgk1 using mouse anti-GFP (1:2000 dilution, 11814460001, Roche), mouse anti-Pgk1 (1:1000 dilution, 459250, Thermo Fisher Scientific) and goat HRP-conjugated anti-mouse (1:5000 dilution, G-21040, Thermo Fisher Scientific) antibodies. .. Membranes were developed using a chemiluminescent horseradish peroxidase substrate (SuperSignal West Pico PLUS, 34580, Thermo Fisher Scientific) and imaged using a ChemiDoc MP imaging system (Bio-Rad).

    Incubation:

    Article Title: Duplicated ribosomal protein paralogs promote alternative translation and drug resistance.
    Article Snippet: Protein samples (20 μg)were separated on 15% SDS-PAGE and transferred to Protran nitrocellulose membranes (GE Healthcare). .. Membranes were blocked overnight at 4 °C with 5% milk in TBS-T (20mM Tris pH 7.6, 150mM NaCl, 0.1% Tween-20), then incubated overnight at 4 °C with the following primary antibodies: rabbit anti-L7 (Bethyl Laboratories, cat#A3100-741A-M, 1:1000), rabbit anti-L5 (kindly provided by Woolford lab, 1:2000), mouse anti-L3 (kindly provided by the Warner lab, 1:5000) and mouse anti-Pgk1 (Invitrogen/Thermo Fisher, cat#459250, 1:10,000) diluted in blocking solution. .. After washing with 4 changes of TBS-T over 40min, the membranes were incubated for 90min at room temperature with secondary antibodies (donkey anti-rabbit HRP-IgG, GE Healthacare, cat#NA934V, 1:5000 or goat anti-mouse HRP-IgG, GE Healthcare, cat#NA931V, 1:2000) diluted in blocking solution and washed as before.

    Blocking Assay:

    Article Title: Duplicated ribosomal protein paralogs promote alternative translation and drug resistance.
    Article Snippet: Protein samples (20 μg)were separated on 15% SDS-PAGE and transferred to Protran nitrocellulose membranes (GE Healthcare). .. Membranes were blocked overnight at 4 °C with 5% milk in TBS-T (20mM Tris pH 7.6, 150mM NaCl, 0.1% Tween-20), then incubated overnight at 4 °C with the following primary antibodies: rabbit anti-L7 (Bethyl Laboratories, cat#A3100-741A-M, 1:1000), rabbit anti-L5 (kindly provided by Woolford lab, 1:2000), mouse anti-L3 (kindly provided by the Warner lab, 1:5000) and mouse anti-Pgk1 (Invitrogen/Thermo Fisher, cat#459250, 1:10,000) diluted in blocking solution. .. After washing with 4 changes of TBS-T over 40min, the membranes were incubated for 90min at room temperature with secondary antibodies (donkey anti-rabbit HRP-IgG, GE Healthacare, cat#NA934V, 1:5000 or goat anti-mouse HRP-IgG, GE Healthcare, cat#NA931V, 1:2000) diluted in blocking solution and washed as before.



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    Image Search Results


    ( A ) Epitope-tagged strains of various proteins involved in the de novo biosynthesis of sulfur-containing amino acids, including Met4, Met32, Met16, Met10, Cys4, and Cys3 were spotted on SLAD in the presence and absence of sub-inhibitory concentration of 2-Deoxy-D-Glucose (2DG) following which, cells from colonies were isolated at day 5 and levels of these proteins were assessed using Western blotting. Raw images of Western blots were analyzed using ImageJ to normalize targeted protein expression with the expression of housekeeping protein- β-actin, in order to generate densitometric graphs. Statistical analysis was done using unpaired t-test, **(p<0.01) and *(p<0.05). Error bars represent SEM. ( B ) Epitope-tagged strains of various proteins involved in the de novo biosynthesis of sulfur-containing amino acids, including Met32, Met16, Met10, and Cys3 were grown in liquid SLAD and then treated with sub-inhibitory concentration of 2DG for 24 hr after which protein expression was checked using Western blotting. Pgk1 was used as loading control. ( C ) Raw images of Western blots were analyzed using ImageJ to normalize targeted protein expression with the expression of housekeeping protein-Pgk1, in order to generate densitometric graphs. Statistical analysis was done using unpaired t-test, ***(p<0.001), **(p<0.01) and *(p<0.05). Error bars represent SEM. This figure was created using Biorender.com. Figure 2—figure supplement 2—source data 1. Uncropped and labeled blots for . Figure 2—figure supplement 2—source data 2. Raw unedited blots for .

    Journal: eLife

    Article Title: Glycolysis-dependent sulfur metabolism orchestrates morphological plasticity and virulence in fungi

    doi: 10.7554/eLife.109075

    Figure Lengend Snippet: ( A ) Epitope-tagged strains of various proteins involved in the de novo biosynthesis of sulfur-containing amino acids, including Met4, Met32, Met16, Met10, Cys4, and Cys3 were spotted on SLAD in the presence and absence of sub-inhibitory concentration of 2-Deoxy-D-Glucose (2DG) following which, cells from colonies were isolated at day 5 and levels of these proteins were assessed using Western blotting. Raw images of Western blots were analyzed using ImageJ to normalize targeted protein expression with the expression of housekeeping protein- β-actin, in order to generate densitometric graphs. Statistical analysis was done using unpaired t-test, **(p<0.01) and *(p<0.05). Error bars represent SEM. ( B ) Epitope-tagged strains of various proteins involved in the de novo biosynthesis of sulfur-containing amino acids, including Met32, Met16, Met10, and Cys3 were grown in liquid SLAD and then treated with sub-inhibitory concentration of 2DG for 24 hr after which protein expression was checked using Western blotting. Pgk1 was used as loading control. ( C ) Raw images of Western blots were analyzed using ImageJ to normalize targeted protein expression with the expression of housekeeping protein-Pgk1, in order to generate densitometric graphs. Statistical analysis was done using unpaired t-test, ***(p<0.001), **(p<0.01) and *(p<0.05). Error bars represent SEM. This figure was created using Biorender.com. Figure 2—figure supplement 2—source data 1. Uncropped and labeled blots for . Figure 2—figure supplement 2—source data 2. Raw unedited blots for .

    Article Snippet: Pgk1 Mouse mAb (Cat. #sc-130335) was purchased from Santa Cruz Biotechnology.

    Techniques: Concentration Assay, Isolation, Western Blot, Expressing, Control, Labeling