rabbit ca v β2  (Alomone Labs)


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    Alomone Labs rabbit ca v β2
    Expression of <t>Ca</t> <t>V</t> α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V <t>β2</t> ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.
    Rabbit Ca V β2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit ca v β2/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit ca v β2 - by Bioz Stars, 2023-02
    94/100 stars

    Images

    1) Product Images from "Sympathetic Stimulation Upregulates the Ca 2+ Channel Subunit, Ca V α2δ1, via the β1 and ERK 1/2 Pathway in Neonatal Ventricular Cardiomyocytes"

    Article Title: Sympathetic Stimulation Upregulates the Ca 2+ Channel Subunit, Ca V α2δ1, via the β1 and ERK 1/2 Pathway in Neonatal Ventricular Cardiomyocytes

    Journal: Cells

    doi: 10.3390/cells11020188

    Expression of Ca V α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V β2 ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.
    Figure Legend Snippet: Expression of Ca V α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V β2 ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.

    Techniques Used: Expressing, Incubation

    rabbit ca v β2  (Alomone Labs)


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  • 94

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    Alomone Labs rabbit ca v β2
    Expression of <t>Ca</t> <t>V</t> α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V <t>β2</t> ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.
    Rabbit Ca V β2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit ca v β2/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit ca v β2 - by Bioz Stars, 2023-02
    94/100 stars

    Images

    1) Product Images from "Sympathetic Stimulation Upregulates the Ca 2+ Channel Subunit, Ca V α2δ1, via the β1 and ERK 1/2 Pathway in Neonatal Ventricular Cardiomyocytes"

    Article Title: Sympathetic Stimulation Upregulates the Ca 2+ Channel Subunit, Ca V α2δ1, via the β1 and ERK 1/2 Pathway in Neonatal Ventricular Cardiomyocytes

    Journal: Cells

    doi: 10.3390/cells11020188

    Expression of Ca V α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V β2 ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.
    Figure Legend Snippet: Expression of Ca V α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V β2 ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.

    Techniques Used: Expressing, Incubation

    acc 105  (Alomone Labs)


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    Alomone Labs acc 105
    Acc 105, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acc 105/product/Alomone Labs
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    acc 105 - by Bioz Stars, 2023-02
    94/100 stars

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    acc 105  (Alomone Labs)


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    Alomone Labs acc 105
    Acc 105, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acc 105/product/Alomone Labs
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    acc 105 - by Bioz Stars, 2023-02
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    ca 2 β2 voltage gated channel acc 105  (Alomone Labs)


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    Alomone Labs ca 2 β2 voltage gated channel acc 105
    Antibodies used in the current study with corresponding dilutions and origin
    Ca 2 β2 Voltage Gated Channel Acc 105, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ca 2 β2 voltage gated channel acc 105/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
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    ca 2 β2 voltage gated channel acc 105 - by Bioz Stars, 2023-02
    94/100 stars

    Images

    1) Product Images from "Efficient stimulus-secretion coupling at ribbon synapses requires RIM-binding protein tethering of L-type Ca 2+ channels"

    Article Title: Efficient stimulus-secretion coupling at ribbon synapses requires RIM-binding protein tethering of L-type Ca 2+ channels

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    doi: 10.1073/pnas.1702991114

    Antibodies used in the current study with corresponding dilutions and origin
    Figure Legend Snippet: Antibodies used in the current study with corresponding dilutions and origin

    Techniques Used:

    ca 2 β2 voltage gated channel acc 105  (Alomone Labs)


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    Alomone Labs ca 2 β2 voltage gated channel acc 105
    Antibodies used in the current study with corresponding dilutions and origin
    Ca 2 β2 Voltage Gated Channel Acc 105, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ca 2 β2 voltage gated channel acc 105/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    ca 2 β2 voltage gated channel acc 105 - by Bioz Stars, 2023-02
    94/100 stars

    Images

    1) Product Images from "Efficient stimulus-secretion coupling at ribbon synapses requires RIM-binding protein tethering of L-type Ca 2+ channels"

    Article Title: Efficient stimulus-secretion coupling at ribbon synapses requires RIM-binding protein tethering of L-type Ca 2+ channels

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    doi: 10.1073/pnas.1702991114

    Antibodies used in the current study with corresponding dilutions and origin
    Figure Legend Snippet: Antibodies used in the current study with corresponding dilutions and origin

    Techniques Used:

    rabbit anti β 2  (Alomone Labs)


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    Alomone Labs rabbit anti β 2
    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V <t>β</t> <t>2</t> subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
    Rabbit Anti β 2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti β 2/product/Alomone Labs
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    rabbit anti β 2 - by Bioz Stars, 2023-02
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    Images

    1) Product Images from "Aberrant Splicing Promotes Proteasomal Degradation of L-type Ca V 1.2 Calcium Channels by Competitive Binding for Ca V β Subunits in Cardiac Hypertrophy"

    Article Title: Aberrant Splicing Promotes Proteasomal Degradation of L-type Ca V 1.2 Calcium Channels by Competitive Binding for Ca V β Subunits in Cardiac Hypertrophy

    Journal: Scientific Reports

    doi: 10.1038/srep35247

    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V β 2 subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
    Figure Legend Snippet: ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V β 2 subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.

    Techniques Used: Expressing

    polyclonal antibody  (Alomone Labs)


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    Alomone Labs polyclonal antibody
    Polyclonal Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti ca v β 2 subunit antibody  (Alomone Labs)


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    Alomone Labs anti ca v β 2 subunit antibody
    Anti Ca V β 2 Subunit Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti cav β2 subunit antibody  (Alomone Labs)


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    Alomone Labs anti cav β2 subunit antibody
    Anti Cav β2 Subunit Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    b2  (Alomone Labs)


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    Alomone Labs b2
    B2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Alomone Labs rabbit ca v β2
    Expression of <t>Ca</t> <t>V</t> α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V <t>β2</t> ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.
    Rabbit Ca V β2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit ca v β2/product/Alomone Labs
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    Alomone Labs acc 105
    Expression of <t>Ca</t> <t>V</t> α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V <t>β2</t> ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.
    Acc 105, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acc 105/product/Alomone Labs
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    Alomone Labs ca 2 β2 voltage gated channel acc 105
    Antibodies used in the current study with corresponding dilutions and origin
    Ca 2 β2 Voltage Gated Channel Acc 105, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ca 2 β2 voltage gated channel acc 105/product/Alomone Labs
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    Alomone Labs rabbit anti β 2
    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V <t>β</t> <t>2</t> subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
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    Alomone Labs polyclonal antibody
    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V <t>β</t> <t>2</t> subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
    Polyclonal Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Alomone Labs anti ca v β 2 subunit antibody
    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V <t>β</t> <t>2</t> subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
    Anti Ca V β 2 Subunit Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Alomone Labs anti cav β2 subunit antibody
    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V <t>β</t> <t>2</t> subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
    Anti Cav β2 Subunit Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Alomone Labs b2
    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V <t>β</t> <t>2</t> subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.
    B2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/b2/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    b2 - by Bioz Stars, 2023-02
    94/100 stars
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    Image Search Results


    Expression of Ca V α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V β2 ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.

    Journal: Cells

    Article Title: Sympathetic Stimulation Upregulates the Ca 2+ Channel Subunit, Ca V α2δ1, via the β1 and ERK 1/2 Pathway in Neonatal Ventricular Cardiomyocytes

    doi: 10.3390/cells11020188

    Figure Lengend Snippet: Expression of Ca V α2δ1 ( A ), Ca V α1C ( C ), Ca V β3 ( E ), and Ca V β2 ( G ) in neonatal rat cardiomyocytes. Total proteins were extracted from neonatal rat ventricular cardiomyocytes. Proteins were separated on an 8% SDS-polyacrylamide gel, transferred to a nitrocellulose membrane, and probed with anti-Ca V α2δ1, anti-Ca V α1C, anti-Ca V β3, anti-Ca V β2, and anti-GAPDH antibodies overnight and then incubated with HRP-conjugated goat anti-rabbit secondary antibody. Lanes were loaded with 30 μg of proteins. NE: cardiomyocytes treated with 1 µM norepinephrine. Graph showing the total protein expression of Ca V α2δ1 ( B ), Ca V α1C ( D ), Ca V β3 ( F ), and Ca V β2 ( H ) normalized to GAPDH. * p < 0.01 vs. Basal. Statistical analysis was performed using one-way ANOVA.

    Article Snippet: Antibodies used were rabbit anti-Ca V α2δ1 (1:1000, Alomone ACC-015), rabbit Ca V α1C (1:1000, Alomone ACC-003), rabbit Ca V β2 (1:5000, Alomone ACC-105), rabbit Ca V β3 (1:500, Alomone ACC-008), rabbit Phospho-ERK 1/2 (Cell Signaling Technology, Danvers, MA, USA, 9101S), Total ERK 1/2 (Cell Signaling Technology, 137F5) and rabbit GAPDH (Jackson, West Grove, PA, USA, 111-035-144).

    Techniques: Expressing, Incubation

    Antibodies used in the current study with corresponding dilutions and origin

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Efficient stimulus-secretion coupling at ribbon synapses requires RIM-binding protein tethering of L-type Ca 2+ channels

    doi: 10.1073/pnas.1702991114

    Figure Lengend Snippet: Antibodies used in the current study with corresponding dilutions and origin

    Article Snippet: A list of antibodies used in the current study with corresponding dilutions and origin are presented in . table ft1 table-wrap mode="anchored" t5 Table S1. caption a7 Antigen Antibody Dilution Active zone proteins RBP-1 (RIM-binding protein-1) 316003 (SySy) 1:1,000 RBP-2 (RIM-binding protein-2) 316103 (SySy) 1:1,000 RBP-2 (RIM-binding protein-2) 4193 (custom) 1:1,000 RIM 1 (RIM1 central domains) R809 (custom) 1:2,000 RIM 1/2 (1α/2α N terminus + rabphillin) U1565 (custom) 1:2,000 Liprin α3 4396 (custom) 1:5,000 ELKS 1/2aB 4790 (custom) 1:500 CASK 75–000 (Neuromab) 1:1,000 Mint1 P932 (custom) 1;1000 Veli1,2,3 T813 (custom) 1:1,000 Munc13-1 126103 (SySy) 1:1,000 Ribeye Maxeiner et al. ( 32 ) 1:1,000 Ca 2+ channels Ca 2+ v1.2-α1C voltage-gated channel ACC-003 (Alomone) 1:200 Ca 2+ v1.3-α1D voltage-gated channel ACC-005 (Alomone) 1:200 Ca 2+ v1.4-α1D voltage-gated channel Gift from Frank Schmitz 1:1,000 Ca 2+ v-α2δ1 voltage-gated channel ACC-015 (Alomone) 1:500 Ca 2+ v-α2δ2 voltage-gated channel ACC-102 (Alomone) 1:500 Ca 2+ v-α2δ3 voltage-gated channel ACC-103 (Alomone) 1:500 Ca 2+ v-α2δ4 voltage-gated channel ACC-104 (Alomone) 1:500 Ca 2+ β1 voltage-gated channel ACC-106 (Alomone) 1:250 Ca 2+ β2 voltage-gated channel ACC-105 (Alomone) 1:250 Ca 2+ β3 voltage-gated channel ACC-108 (Alomone) 1:250 Ca 2+ β4 voltage-gated channel 75–054 (Neuromab) 1:250 Exocytosis proteins Syntaxin 1 HPC-1 (custom) 1:500 SNAP 25 71.1 (custom) 1:2,000 Synaptobrevin 2 69.1 (custom) 1:2,500 Synaptotagmin 1 41.1 (custom) 1:1,000 Loading control TUJ1 T2200 (Sigma) 1:5,000 Open in a separate window Antibodies used in the current study with corresponding dilutions and origin

    Techniques:

    ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V β 2 subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.

    Journal: Scientific Reports

    Article Title: Aberrant Splicing Promotes Proteasomal Degradation of L-type Ca V 1.2 Calcium Channels by Competitive Binding for Ca V β Subunits in Cardiac Hypertrophy

    doi: 10.1038/srep35247

    Figure Lengend Snippet: ( A ) Increased ratio of left ventricle to body weight in TAC mice. ( B ) Representative M-mode echocardiography images of mouse hearts before and 14 days after TAC surgery indicating progression of cardiac hypertrophy. ( C ) Increased LVAWd and LVPWd in TAC mice. ( D ) Representative gel photos for transcript screening of exons 21 + 22 inclusion level. Each lane represents a single colony expressing exons 21 + 22 or exon 21/22. ( E ) Inclusion level of exons 21 + 22 increased from 0.52% to 6.49% with the development of cardiac hypertrophy induced by pressure overload within 14 days (n = 6). ( F – H ) Expression levels of total Ca V 1.2 channels and Ca V β 2 subunits in left ventricles (n = 8). ( I , J ) Ubiquitination level of cardiac Ca V 1.2 channels in left ventricles (n = 8). Data were shown as mean ± SEM. * p < 0.05, # p < 0.01. 1-way ANOVA was performed for multiple comparisons in panel E.

    Article Snippet: Subsequently, the membrane was blocked with 5% non-fat milk for 1h at room temperature and then incubated overnight at 4 °C with primary antibodies: rabbit anti-Ca V 1.2 (1:1000, ACC-003, Alomone), anti-Ca V 3.1 (1:1000, ACC-021), rabbit anti-β 2 (1:1000, ACC-105), mouse anti-ubiquitin (1:1000, 13–1600, Invitrogen), rabbit anti-HA (1:1000, 71–5500), mouse anti-TfR (1:1000, 13–6800), mouse anti-β-actin (1:5000, A1978, Sigma) or mouse anti-GAPDH (1:2000, G8795).

    Techniques: Expressing