lif  (Alomone Labs)


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    Structured Review

    Alomone Labs lif
    Lif, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lif/product/Alomone Labs
    Average 86 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    lif - by Bioz Stars, 2022-12
    86/100 stars

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  • 93
    Alomone Labs potassium 4 3 channel subunit kv4 3
    Western blot analysis of ion <t>channel</t> proteins’ expression in left ventricular tissues from various group hearts. Top in each: Representative immunoblot images of ion channel proteins. β‐actin was used as the loading control. Arrow indicates the band used for densitometric quantification. Bottom in each: Mean normalized densitometry of ion channel proteins. Bars represent mean±SD of 8, 13, 8, 12, 9, 12, 14, and 10 hearts in each group for the study of voltage‐gated potassium 4.2 channel <t>subunit</t> <t>(Kv4.2),</t> voltage‐gated potassium 4.3 channel subunit <t>(Kv4.3),</t> voltage‐gated potassium 1.4 channel subunit (Kv1.4), Kv‐channel interacting protein 2 (KChIP2), voltage‐gated potassium 2.1 channel subunit (Kv2.1), inwardly rectifying potassium 2.1 channel subunit (Kir2.1), voltage‐gated L‐type calcium 1.2a channel subunit (Ca V 1.2a), and voltage‐gated sodium 1.5 channel subunit (Na V 1.5), respectively. All measurements were normalized to the protein levels of β‐actin. ** P
    Potassium 4 3 Channel Subunit Kv4 3, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/potassium 4 3 channel subunit kv4 3/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    potassium 4 3 channel subunit kv4 3 - by Bioz Stars, 2022-12
    93/100 stars
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    92
    Alomone Labs potassium 1 4 channel subunit kv1 4
    Western blot analysis of ion <t>channel</t> proteins’ expression in left ventricular tissues from various group hearts. Top in each: Representative immunoblot images of ion channel proteins. β‐actin was used as the loading control. Arrow indicates the band used for densitometric quantification. Bottom in each: Mean normalized densitometry of ion channel proteins. Bars represent mean±SD of 8, 13, 8, 12, 9, 12, 14, and 10 hearts in each group for the study of voltage‐gated potassium 4.2 channel <t>subunit</t> (Kv4.2), voltage‐gated potassium 4.3 channel subunit (Kv4.3), voltage‐gated potassium 1.4 channel subunit <t>(Kv1.4),</t> Kv‐channel interacting protein 2 (KChIP2), voltage‐gated potassium 2.1 channel subunit (Kv2.1), inwardly rectifying potassium 2.1 channel subunit (Kir2.1), voltage‐gated L‐type calcium 1.2a channel subunit (Ca V 1.2a), and voltage‐gated sodium 1.5 channel subunit (Na V 1.5), respectively. All measurements were normalized to the protein levels of β‐actin. ** P
    Potassium 1 4 Channel Subunit Kv1 4, supplied by Alomone Labs, 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/potassium 1 4 channel subunit kv1 4/product/Alomone Labs
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    94
    Alomone Labs anti cav1 3
    Dormant SANC express reduced I <t>Cav1.3</t> and I f . Representative traces and I-V curves of I f (( A ), n = 10 dormant and n = 8 firing) and Nife-sensitive current ( I Cav1.3 ) (( B ), n = 12 dormant and n = 9 firing) in dormant (blue) and firing (red) SANC. ( C ) Nife-sensitive current ( I Cav1.3 ) and Nife-insensitive current ( I Cav1.2 ) densities at 0 mV in dormant and firing Ca v 1.2 DHP−/− SANC. Averaged SR Ca 2+ load ( D ), time constant of caffeine-induced Ca 2+ transient ( E ), number of LCRs ( F ) and diastolic Ca 2+ ( G ), in dormant (blue, n = 9) and firing (red, n = 15) SANC. ns: non-significant, * p
    Anti Cav1 3, 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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    95
    Alomone Labs cav1 2
    Dormant SANC express reduced I <t>Cav1.3</t> and I f . Representative traces and I-V curves of I f (( A ), n = 10 dormant and n = 8 firing) and Nife-sensitive current ( I Cav1.3 ) (( B ), n = 12 dormant and n = 9 firing) in dormant (blue) and firing (red) SANC. ( C ) Nife-sensitive current ( I Cav1.3 ) and Nife-insensitive current ( I Cav1.2 ) densities at 0 mV in dormant and firing Ca v 1.2 DHP−/− SANC. Averaged SR Ca 2+ load ( D ), time constant of caffeine-induced Ca 2+ transient ( E ), number of LCRs ( F ) and diastolic Ca 2+ ( G ), in dormant (blue, n = 9) and firing (red, n = 15) SANC. ns: non-significant, * p
    Cav1 2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Western blot analysis of ion channel proteins’ expression in left ventricular tissues from various group hearts. Top in each: Representative immunoblot images of ion channel proteins. β‐actin was used as the loading control. Arrow indicates the band used for densitometric quantification. Bottom in each: Mean normalized densitometry of ion channel proteins. Bars represent mean±SD of 8, 13, 8, 12, 9, 12, 14, and 10 hearts in each group for the study of voltage‐gated potassium 4.2 channel subunit (Kv4.2), voltage‐gated potassium 4.3 channel subunit (Kv4.3), voltage‐gated potassium 1.4 channel subunit (Kv1.4), Kv‐channel interacting protein 2 (KChIP2), voltage‐gated potassium 2.1 channel subunit (Kv2.1), inwardly rectifying potassium 2.1 channel subunit (Kir2.1), voltage‐gated L‐type calcium 1.2a channel subunit (Ca V 1.2a), and voltage‐gated sodium 1.5 channel subunit (Na V 1.5), respectively. All measurements were normalized to the protein levels of β‐actin. ** P

    Journal: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

    Article Title: Candesartan Cilexetil Attenuates Arrhythmogenicity Following Pressure Overload in Rats via the Modulation of Cardiac Electrical and Structural Remodeling and Calcium Handling Dysfunction

    doi: 10.1161/JAHA.121.024285

    Figure Lengend Snippet: Western blot analysis of ion channel proteins’ expression in left ventricular tissues from various group hearts. Top in each: Representative immunoblot images of ion channel proteins. β‐actin was used as the loading control. Arrow indicates the band used for densitometric quantification. Bottom in each: Mean normalized densitometry of ion channel proteins. Bars represent mean±SD of 8, 13, 8, 12, 9, 12, 14, and 10 hearts in each group for the study of voltage‐gated potassium 4.2 channel subunit (Kv4.2), voltage‐gated potassium 4.3 channel subunit (Kv4.3), voltage‐gated potassium 1.4 channel subunit (Kv1.4), Kv‐channel interacting protein 2 (KChIP2), voltage‐gated potassium 2.1 channel subunit (Kv2.1), inwardly rectifying potassium 2.1 channel subunit (Kir2.1), voltage‐gated L‐type calcium 1.2a channel subunit (Ca V 1.2a), and voltage‐gated sodium 1.5 channel subunit (Na V 1.5), respectively. All measurements were normalized to the protein levels of β‐actin. ** P

    Article Snippet: Membranes were blocked and then incubated overnight at 4 °C with primary antibody against ryanodine receptor Ca2+ release channel 2 (RyR2) (1:1000; ThermoFisher Scientific, Waltham, MA), Ser2808 ‐phosphorylated RyR2 (pSer2808 ‐RyR2) (1:5000; Badrilla, Leeds, United Kingdom), pSer2814 ‐RyR2 (1:500; Badrilla), SERCA2a (sarco[endo]plasmic reticulum Ca2+ ‐ATPase) (1:5000; Badrilla), phospholamban (1:2000; Badrilla), pSer16 ‐phospholamban (1:2000; Millipore, Temecula, CA), pThr17 ‐phospholamban (1:2000; Badrilla), Na+ ‐Ca2+ exchanger 1 (NCX1) (1:500; Santa Cruz Biotechnology, Santa Cruz, CA), voltage‐gated L‐type calcium 1.2a channel subunit (CaV 1.2a) (1:400; Millipore), voltage‐gated sodium 1.5 channel subunit (NaV1.5) (1:500; Alomone, Jerusalem, Israel), voltage‐gated potassium 4.2 channel subunit (Kv4.2) (1:200; Millipore), voltage‐gated potassium 4.3 channel subunit (Kv4.3) (1:200; Alomone), voltage‐gated potassium 1.4 channel subunit (Kv1.4) (1:200; Alomone), Kv‐channel interacting protein 2 (KChIP2) (1:500; ThermoFisher Scientific), voltage‐gated potassium 2.1 channel subunit (Kv2.1) (1:500; Alomone), and inwardly rectifying potassium 2.1 channel subunit (Kir2.1) (1:600; Alomone).

    Techniques: Western Blot, Expressing

    Western blot analysis of ion channel proteins’ expression in left ventricular tissues from various group hearts. Top in each: Representative immunoblot images of ion channel proteins. β‐actin was used as the loading control. Arrow indicates the band used for densitometric quantification. Bottom in each: Mean normalized densitometry of ion channel proteins. Bars represent mean±SD of 8, 13, 8, 12, 9, 12, 14, and 10 hearts in each group for the study of voltage‐gated potassium 4.2 channel subunit (Kv4.2), voltage‐gated potassium 4.3 channel subunit (Kv4.3), voltage‐gated potassium 1.4 channel subunit (Kv1.4), Kv‐channel interacting protein 2 (KChIP2), voltage‐gated potassium 2.1 channel subunit (Kv2.1), inwardly rectifying potassium 2.1 channel subunit (Kir2.1), voltage‐gated L‐type calcium 1.2a channel subunit (Ca V 1.2a), and voltage‐gated sodium 1.5 channel subunit (Na V 1.5), respectively. All measurements were normalized to the protein levels of β‐actin. ** P

    Journal: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

    Article Title: Candesartan Cilexetil Attenuates Arrhythmogenicity Following Pressure Overload in Rats via the Modulation of Cardiac Electrical and Structural Remodeling and Calcium Handling Dysfunction

    doi: 10.1161/JAHA.121.024285

    Figure Lengend Snippet: Western blot analysis of ion channel proteins’ expression in left ventricular tissues from various group hearts. Top in each: Representative immunoblot images of ion channel proteins. β‐actin was used as the loading control. Arrow indicates the band used for densitometric quantification. Bottom in each: Mean normalized densitometry of ion channel proteins. Bars represent mean±SD of 8, 13, 8, 12, 9, 12, 14, and 10 hearts in each group for the study of voltage‐gated potassium 4.2 channel subunit (Kv4.2), voltage‐gated potassium 4.3 channel subunit (Kv4.3), voltage‐gated potassium 1.4 channel subunit (Kv1.4), Kv‐channel interacting protein 2 (KChIP2), voltage‐gated potassium 2.1 channel subunit (Kv2.1), inwardly rectifying potassium 2.1 channel subunit (Kir2.1), voltage‐gated L‐type calcium 1.2a channel subunit (Ca V 1.2a), and voltage‐gated sodium 1.5 channel subunit (Na V 1.5), respectively. All measurements were normalized to the protein levels of β‐actin. ** P

    Article Snippet: Membranes were blocked and then incubated overnight at 4 °C with primary antibody against ryanodine receptor Ca2+ release channel 2 (RyR2) (1:1000; ThermoFisher Scientific, Waltham, MA), Ser2808 ‐phosphorylated RyR2 (pSer2808 ‐RyR2) (1:5000; Badrilla, Leeds, United Kingdom), pSer2814 ‐RyR2 (1:500; Badrilla), SERCA2a (sarco[endo]plasmic reticulum Ca2+ ‐ATPase) (1:5000; Badrilla), phospholamban (1:2000; Badrilla), pSer16 ‐phospholamban (1:2000; Millipore, Temecula, CA), pThr17 ‐phospholamban (1:2000; Badrilla), Na+ ‐Ca2+ exchanger 1 (NCX1) (1:500; Santa Cruz Biotechnology, Santa Cruz, CA), voltage‐gated L‐type calcium 1.2a channel subunit (CaV 1.2a) (1:400; Millipore), voltage‐gated sodium 1.5 channel subunit (NaV1.5) (1:500; Alomone, Jerusalem, Israel), voltage‐gated potassium 4.2 channel subunit (Kv4.2) (1:200; Millipore), voltage‐gated potassium 4.3 channel subunit (Kv4.3) (1:200; Alomone), voltage‐gated potassium 1.4 channel subunit (Kv1.4) (1:200; Alomone), Kv‐channel interacting protein 2 (KChIP2) (1:500; ThermoFisher Scientific), voltage‐gated potassium 2.1 channel subunit (Kv2.1) (1:500; Alomone), and inwardly rectifying potassium 2.1 channel subunit (Kir2.1) (1:600; Alomone).

    Techniques: Western Blot, Expressing

    Dormant SANC express reduced I Cav1.3 and I f . Representative traces and I-V curves of I f (( A ), n = 10 dormant and n = 8 firing) and Nife-sensitive current ( I Cav1.3 ) (( B ), n = 12 dormant and n = 9 firing) in dormant (blue) and firing (red) SANC. ( C ) Nife-sensitive current ( I Cav1.3 ) and Nife-insensitive current ( I Cav1.2 ) densities at 0 mV in dormant and firing Ca v 1.2 DHP−/− SANC. Averaged SR Ca 2+ load ( D ), time constant of caffeine-induced Ca 2+ transient ( E ), number of LCRs ( F ) and diastolic Ca 2+ ( G ), in dormant (blue, n = 9) and firing (red, n = 15) SANC. ns: non-significant, * p

    Journal: Cells

    Article Title: L-Type Cav1.3 Calcium Channels Are Required for Beta-Adrenergic Triggered Automaticity in Dormant Mouse Sinoatrial Pacemaker Cells

    doi: 10.3390/cells11071114

    Figure Lengend Snippet: Dormant SANC express reduced I Cav1.3 and I f . Representative traces and I-V curves of I f (( A ), n = 10 dormant and n = 8 firing) and Nife-sensitive current ( I Cav1.3 ) (( B ), n = 12 dormant and n = 9 firing) in dormant (blue) and firing (red) SANC. ( C ) Nife-sensitive current ( I Cav1.3 ) and Nife-insensitive current ( I Cav1.2 ) densities at 0 mV in dormant and firing Ca v 1.2 DHP−/− SANC. Averaged SR Ca 2+ load ( D ), time constant of caffeine-induced Ca 2+ transient ( E ), number of LCRs ( F ) and diastolic Ca 2+ ( G ), in dormant (blue, n = 9) and firing (red, n = 15) SANC. ns: non-significant, * p

    Article Snippet: SAN was incubated with anti-Cav1.3 (rabbit, 1:200, obtained from [ ] and anti-HCN4 (guinea pig, 1:200, Alomone labs, Cat. AGP-004) primary antibodies at 4 °C overnight.

    Techniques: