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anti cav3 2  (Alomone Labs)


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    Structured Review

    Alomone Labs anti cav3 2
    Anti Cav3 2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+cav3+2/Anti-CaV3%2E2+(CACNA1H)+Antibody/bio_rxiv__64898__2026__03__19__712770-239-26-29
    Average 95 stars, based on 80 article reviews
    anti cav3 2 - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: T-type Ca 2+ channels play a dual role in modulating the excitability of dorsal root ganglia neurons
    Article Snippet: After protein concentrations were determined with BCA assays, the protein samples were separated on a 10% SDS-PAGE gels and transferred to polyvinylidene-fluoride (PVDF) membranes (Merck Millipore). .. After blocking with 3% fat-free dried milk in TBST (20 mM Tris-HCl, 150 mM NaCl, 0.1% Tween 20, pH 7.6) at room temperature for 1 h, PVDF membranes were incubated with mouse anti-Cav3.2 (1:1000, NBP1-22,444ss, Novusbio, Centennial, USA) or mouse anti-Cav3.3 (1:200, Cat#: ACC-009, Alomone Labs, Israel) and anti-β-actin (1:1000, Abcam, USA) antibodies in 3% fat-free dried milk in TBST overnight at 4°C. .. The blots were then washed with TBST, followed by incubation with (1:4000) horseradish-peroxidase-conjugated, goat anti-mouse antibody (Bio-Rad).

    Article Title: Histone methylation-mediated microRNA-32-5p down-regulation in sensory neurons regulates pain behaviors via targeting Cav3.2 channels
    Article Snippet: .. After hybridization, the sections were rinsed in washing buffer (containing formamide and saline-sodium citrate) three times and blocked for 1 h in blocking buffer at 37 °C, followed by incubation in Cy3-labeled anti-digoxin antibody (diluted in blocking buffer at 1:150) for 1 h. For co-labeling experiments, the sections were first hybridized with the probe of miRNA-32-5p, then co-incubated with rabbit anti-Cav3.2 (1:300, Alomone Labs), mouse anti-H3K9me2 (1:500, Abcam), mouse anti- H3K27me3 (1:500, Abcam), and rabbit anti-GR (1:300, Cell Signaling Technology), respectively, overnight at 4 °C. .. The fluorescent signals were developed with appropriate fluorescence conjugated secondary antibodies including DyLight 488-conjugated goat antirabbit IgG (1:300, Cell Signaling Technology) or DyLight 488-conjugated goat anti-mouse IgG (1:300, Cell Signaling Technology).

    Incubation:

    Article Title: T-type Ca 2+ channels play a dual role in modulating the excitability of dorsal root ganglia neurons
    Article Snippet: After protein concentrations were determined with BCA assays, the protein samples were separated on a 10% SDS-PAGE gels and transferred to polyvinylidene-fluoride (PVDF) membranes (Merck Millipore). .. After blocking with 3% fat-free dried milk in TBST (20 mM Tris-HCl, 150 mM NaCl, 0.1% Tween 20, pH 7.6) at room temperature for 1 h, PVDF membranes were incubated with mouse anti-Cav3.2 (1:1000, NBP1-22,444ss, Novusbio, Centennial, USA) or mouse anti-Cav3.3 (1:200, Cat#: ACC-009, Alomone Labs, Israel) and anti-β-actin (1:1000, Abcam, USA) antibodies in 3% fat-free dried milk in TBST overnight at 4°C. .. The blots were then washed with TBST, followed by incubation with (1:4000) horseradish-peroxidase-conjugated, goat anti-mouse antibody (Bio-Rad).

    Article Title: Cav3.2 T-Type calcium channels downregulation attenuates bone cancer pain induced by inhibiting IGF-1/HIF-1α signaling pathway in the rat spinal cord
    Article Snippet: According to a standard protocol, an equal amount (40 μg) of protein was separated from each sample on 8% – 12% SDS-PAGE and transferred to the polyvinylidene fluoride membrane (Merck Millipore). .. The blots were blocked in a solution of 5% non-fat milk with TBST (20 mM Tris-HCl, pH 7.6, 150 mM NaCl, 0.05% Tween 20) for 1 h at room temperature and incubated with one of the following primary antibodies at 4 °C overnight: rabbit anti-Cav3.2 (1: 200, ACC-025, Alomone Labs), rabbit anti-IGF-1 (1: 1000, 28530-1-AP, Proteintech), rabbit anti-IGF-1R β (1:1000, 3027S, Cell Signaling Technology), rabbit anti-HIF-1α (1: 2000, 20960-1-AP, Proteintech), rabbit anti-β-tubulin (1: 1000, ab179513, Abcam), or rabbit anti- Histone-H3 (1: 3000, 17168-1-AP, Proteintech). .. Subsequently, after washing with TBST 3 times (5 min each time), membranes were incubated with horseradish peroxidase-conjugated goat anti-rabbit secondary antibody (1:10000, A21020, abbkine) for 1 h at room temperature.

    Article Title: Histone methylation-mediated microRNA-32-5p down-regulation in sensory neurons regulates pain behaviors via targeting Cav3.2 channels
    Article Snippet: .. After hybridization, the sections were rinsed in washing buffer (containing formamide and saline-sodium citrate) three times and blocked for 1 h in blocking buffer at 37 °C, followed by incubation in Cy3-labeled anti-digoxin antibody (diluted in blocking buffer at 1:150) for 1 h. For co-labeling experiments, the sections were first hybridized with the probe of miRNA-32-5p, then co-incubated with rabbit anti-Cav3.2 (1:300, Alomone Labs), mouse anti-H3K9me2 (1:500, Abcam), mouse anti- H3K27me3 (1:500, Abcam), and rabbit anti-GR (1:300, Cell Signaling Technology), respectively, overnight at 4 °C. .. The fluorescent signals were developed with appropriate fluorescence conjugated secondary antibodies including DyLight 488-conjugated goat antirabbit IgG (1:300, Cell Signaling Technology) or DyLight 488-conjugated goat anti-mouse IgG (1:300, Cell Signaling Technology).

    Cell-Signaling:

    Article Title: Cav3.2 T-Type calcium channels downregulation attenuates bone cancer pain induced by inhibiting IGF-1/HIF-1α signaling pathway in the rat spinal cord
    Article Snippet: According to a standard protocol, an equal amount (40 μg) of protein was separated from each sample on 8% – 12% SDS-PAGE and transferred to the polyvinylidene fluoride membrane (Merck Millipore). .. The blots were blocked in a solution of 5% non-fat milk with TBST (20 mM Tris-HCl, pH 7.6, 150 mM NaCl, 0.05% Tween 20) for 1 h at room temperature and incubated with one of the following primary antibodies at 4 °C overnight: rabbit anti-Cav3.2 (1: 200, ACC-025, Alomone Labs), rabbit anti-IGF-1 (1: 1000, 28530-1-AP, Proteintech), rabbit anti-IGF-1R β (1:1000, 3027S, Cell Signaling Technology), rabbit anti-HIF-1α (1: 2000, 20960-1-AP, Proteintech), rabbit anti-β-tubulin (1: 1000, ab179513, Abcam), or rabbit anti- Histone-H3 (1: 3000, 17168-1-AP, Proteintech). .. Subsequently, after washing with TBST 3 times (5 min each time), membranes were incubated with horseradish peroxidase-conjugated goat anti-rabbit secondary antibody (1:10000, A21020, abbkine) for 1 h at room temperature.

    Article Title: Histone methylation-mediated microRNA-32-5p down-regulation in sensory neurons regulates pain behaviors via targeting Cav3.2 channels
    Article Snippet: .. After hybridization, the sections were rinsed in washing buffer (containing formamide and saline-sodium citrate) three times and blocked for 1 h in blocking buffer at 37 °C, followed by incubation in Cy3-labeled anti-digoxin antibody (diluted in blocking buffer at 1:150) for 1 h. For co-labeling experiments, the sections were first hybridized with the probe of miRNA-32-5p, then co-incubated with rabbit anti-Cav3.2 (1:300, Alomone Labs), mouse anti-H3K9me2 (1:500, Abcam), mouse anti- H3K27me3 (1:500, Abcam), and rabbit anti-GR (1:300, Cell Signaling Technology), respectively, overnight at 4 °C. .. The fluorescent signals were developed with appropriate fluorescence conjugated secondary antibodies including DyLight 488-conjugated goat antirabbit IgG (1:300, Cell Signaling Technology) or DyLight 488-conjugated goat anti-mouse IgG (1:300, Cell Signaling Technology).

    Hybridization:

    Article Title: Histone methylation-mediated microRNA-32-5p down-regulation in sensory neurons regulates pain behaviors via targeting Cav3.2 channels
    Article Snippet: .. After hybridization, the sections were rinsed in washing buffer (containing formamide and saline-sodium citrate) three times and blocked for 1 h in blocking buffer at 37 °C, followed by incubation in Cy3-labeled anti-digoxin antibody (diluted in blocking buffer at 1:150) for 1 h. For co-labeling experiments, the sections were first hybridized with the probe of miRNA-32-5p, then co-incubated with rabbit anti-Cav3.2 (1:300, Alomone Labs), mouse anti-H3K9me2 (1:500, Abcam), mouse anti- H3K27me3 (1:500, Abcam), and rabbit anti-GR (1:300, Cell Signaling Technology), respectively, overnight at 4 °C. .. The fluorescent signals were developed with appropriate fluorescence conjugated secondary antibodies including DyLight 488-conjugated goat antirabbit IgG (1:300, Cell Signaling Technology) or DyLight 488-conjugated goat anti-mouse IgG (1:300, Cell Signaling Technology).

    Saline:

    Article Title: Histone methylation-mediated microRNA-32-5p down-regulation in sensory neurons regulates pain behaviors via targeting Cav3.2 channels
    Article Snippet: .. After hybridization, the sections were rinsed in washing buffer (containing formamide and saline-sodium citrate) three times and blocked for 1 h in blocking buffer at 37 °C, followed by incubation in Cy3-labeled anti-digoxin antibody (diluted in blocking buffer at 1:150) for 1 h. For co-labeling experiments, the sections were first hybridized with the probe of miRNA-32-5p, then co-incubated with rabbit anti-Cav3.2 (1:300, Alomone Labs), mouse anti-H3K9me2 (1:500, Abcam), mouse anti- H3K27me3 (1:500, Abcam), and rabbit anti-GR (1:300, Cell Signaling Technology), respectively, overnight at 4 °C. .. The fluorescent signals were developed with appropriate fluorescence conjugated secondary antibodies including DyLight 488-conjugated goat antirabbit IgG (1:300, Cell Signaling Technology) or DyLight 488-conjugated goat anti-mouse IgG (1:300, Cell Signaling Technology).

    other:

    Article Title: Effects of progesterone on T-type-Ca 2+ -channel expression in Purkinje cells.
    Article Snippet: Immunostaining of 12-μm-thick cryosections was performed on SuperFrost Plus Adhesion slides (Thermo Fisher Scientific, Waltham, MA, USA, J1800AMNZ).

    Article Title: Effects of progesterone on T-type-Ca 2+ -channel expression in Purkinje cells
    Article Snippet: The next day, after thorough washing with PBS (2 × 2 minutes plus 2 × 10 minutes), the samples were incubated with goat anti-mouse tetramethylrhodamine (TRITC) antibody (1:1000 in PBS T5393, MilliporeSigma; RRID: AB_261699) at room temperature for 2 hours.



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    Alomone Labs cav3 2
    All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and <t>CaV3.1</t> ( d <t>),</t> <t>CaV3.2</t> ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).
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    Image Search Results


    All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and CaV3.1 ( d ), CaV3.2 ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).

    Journal: Nature Communications

    Article Title: Endothelin-3 and T-type Ca 2+ channels drive enteric neural crest cell calcium activity, contractility and migration

    doi: 10.1038/s41467-025-68121-5

    Figure Lengend Snippet: All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and CaV3.1 ( d ), CaV3.2 ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).

    Article Snippet: After fixation, blocking and permeation, samples were incubated for 1 day in 1:200 mouse Anti-SOX10 and 1:100 rabbit anti CaV3.1 (Alomone Labs #ACC-021) or 1:100 rabbit anti CaV3.2 (Alomone Labs #ACC-025) or 1:100 rabbit anti CaV3.3 (Alomone Labs #ACC-009) for 24 h, washed 3 times, incubated in secondary 1:500 anti-mouse Cy3 and 1:500 anti-rabbit AF647 antibody for another day, washed and imaged.

    Techniques: Control, Two Tailed Test