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  • 93
    Alomone Labs kv4 2
    Kv4 2, 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/kv4 2/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    88
    NeuroMab kv4 2
    Bidirectional changes in NMDA receptors and <t>Kv4.2</t> channels are associated with similar changes in mRNA binding to FMRP. FMRP was immunoprecipitated from homogenates of hippocampal tissue obtained from control and chronic ethanol (75 mM) exposed hippocampal
    Kv4 2, supplied by NeuroMab, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kv4 2/product/NeuroMab
    Average 88 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kv4 2 - by Bioz Stars, 2022-10
    88/100 stars
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    kv4 2  (Abcam)
    85
    Abcam kv4 2
    Protein expression quantified by Western blot for <t>Kv4.2</t> and KChIP2 subunits. A , a representative blot showing Kv4.2, KChIP2 and GAPDH in the presence and absence of chronic ISO (48 h). B , quantifications of the Kv4.2 and KChIP2 show decreases in the presence of ISO compared with control (untreated). *, p
    Kv4 2, supplied by Abcam, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kv4 2/product/Abcam
    Average 85 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kv4 2 - by Bioz Stars, 2022-10
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    kv4 2  (Roche)
    88
    Roche kv4 2
    Blockade of phosphorylation at the PKC sites increases the surface expression of <t>Kv4.2</t> channels in COS-7 cells
    Kv4 2, supplied by Roche, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kv4 2/product/Roche
    Average 88 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kv4 2 - by Bioz Stars, 2022-10
    88/100 stars
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    Image Search Results


    Bidirectional changes in NMDA receptors and Kv4.2 channels are associated with similar changes in mRNA binding to FMRP. FMRP was immunoprecipitated from homogenates of hippocampal tissue obtained from control and chronic ethanol (75 mM) exposed hippocampal

    Journal: Alcoholism, clinical and experimental research

    Article Title: FMRP mediates chronic ethanol induced changes in NMDA, Kv4.2, and KChIP3 expression in the hippocampus

    doi: 10.1111/acer.13060

    Figure Lengend Snippet: Bidirectional changes in NMDA receptors and Kv4.2 channels are associated with similar changes in mRNA binding to FMRP. FMRP was immunoprecipitated from homogenates of hippocampal tissue obtained from control and chronic ethanol (75 mM) exposed hippocampal

    Article Snippet: Western blot analysis confirmed successful immmunoprecipitation of FMRP in both control and ethanol-exposed samples (not shown), and RT-qPCR confirmed that mRNA transcripts that code for GluN1, GluN2B, Kv4.2, and KChIP3 co-IP with FMRP ( ).

    Techniques: Binding Assay, Immunoprecipitation

    Model of chronic ethanol induced homeostatic bidirectional changes in expression of NMDA and Kv4.2 channels, and the role of KChIP3 and FMRP in this activity-dependent process. Left panel depicts regulation of the surface expression of NMDA receptors

    Journal: Alcoholism, clinical and experimental research

    Article Title: FMRP mediates chronic ethanol induced changes in NMDA, Kv4.2, and KChIP3 expression in the hippocampus

    doi: 10.1111/acer.13060

    Figure Lengend Snippet: Model of chronic ethanol induced homeostatic bidirectional changes in expression of NMDA and Kv4.2 channels, and the role of KChIP3 and FMRP in this activity-dependent process. Left panel depicts regulation of the surface expression of NMDA receptors

    Article Snippet: Western blot analysis confirmed successful immmunoprecipitation of FMRP in both control and ethanol-exposed samples (not shown), and RT-qPCR confirmed that mRNA transcripts that code for GluN1, GluN2B, Kv4.2, and KChIP3 co-IP with FMRP ( ).

    Techniques: Expressing, Activity Assay

    Inhibition of S6K1 prevents ethanol-induced changes in binding of NMDA and Kv4.2 mRNA transcripts to FMRP. (A) In organotypic hippocampal slice cultures, neither ethanol, (75 mM), the S6K1 inhibitor PF-470861 (PF, 6 μM) alone or ethanol plus PF

    Journal: Alcoholism, clinical and experimental research

    Article Title: FMRP mediates chronic ethanol induced changes in NMDA, Kv4.2, and KChIP3 expression in the hippocampus

    doi: 10.1111/acer.13060

    Figure Lengend Snippet: Inhibition of S6K1 prevents ethanol-induced changes in binding of NMDA and Kv4.2 mRNA transcripts to FMRP. (A) In organotypic hippocampal slice cultures, neither ethanol, (75 mM), the S6K1 inhibitor PF-470861 (PF, 6 μM) alone or ethanol plus PF

    Article Snippet: Western blot analysis confirmed successful immmunoprecipitation of FMRP in both control and ethanol-exposed samples (not shown), and RT-qPCR confirmed that mRNA transcripts that code for GluN1, GluN2B, Kv4.2, and KChIP3 co-IP with FMRP ( ).

    Techniques: Inhibition, Binding Assay

    Chronic ethanol exposure induces bidirectional changes in the expression of NMDA and Kv4.2 receptors in the hippocampus. (A) In an in-vivo model of chronic intermittent ethanol exposure (CIE), immunoblot analysis of the expression of GluN1 and GluN2B

    Journal: Alcoholism, clinical and experimental research

    Article Title: FMRP mediates chronic ethanol induced changes in NMDA, Kv4.2, and KChIP3 expression in the hippocampus

    doi: 10.1111/acer.13060

    Figure Lengend Snippet: Chronic ethanol exposure induces bidirectional changes in the expression of NMDA and Kv4.2 receptors in the hippocampus. (A) In an in-vivo model of chronic intermittent ethanol exposure (CIE), immunoblot analysis of the expression of GluN1 and GluN2B

    Article Snippet: Western blot analysis confirmed successful immmunoprecipitation of FMRP in both control and ethanol-exposed samples (not shown), and RT-qPCR confirmed that mRNA transcripts that code for GluN1, GluN2B, Kv4.2, and KChIP3 co-IP with FMRP ( ).

    Techniques: Expressing, In Vivo

    Protein expression quantified by Western blot for Kv4.2 and KChIP2 subunits. A , a representative blot showing Kv4.2, KChIP2 and GAPDH in the presence and absence of chronic ISO (48 h). B , quantifications of the Kv4.2 and KChIP2 show decreases in the presence of ISO compared with control (untreated). *, p

    Journal: The Journal of Biological Chemistry

    Article Title: Reductions in the Cardiac Transient Outward K+ Current Ito Caused by Chronic β-Adrenergic Receptor Stimulation Are Partly Rescued by Inhibition of Nuclear Factor κB *

    doi: 10.1074/jbc.M115.694984

    Figure Lengend Snippet: Protein expression quantified by Western blot for Kv4.2 and KChIP2 subunits. A , a representative blot showing Kv4.2, KChIP2 and GAPDH in the presence and absence of chronic ISO (48 h). B , quantifications of the Kv4.2 and KChIP2 show decreases in the presence of ISO compared with control (untreated). *, p

    Article Snippet: For GAPDH detection, blots for Kv4.2 and KChIP2 were first stripped using commercial stripping buffer (ST010, GeBa) according to manufacturer's instructions.

    Techniques: Expressing, Western Blot

    NF-κB inhibition partly reverses decreases in I to,f caused by chronic β-AR stimulation. IkBαSA (adenovirally infected) was used to inhibit NF-κB signaling. A , representative current I to,f current traces. B , averaged I to,f current densities at +60 mV for GFP, GFP+ISO, IkBαSA and IkBαSA+ISO. C , relative mRNA expression for KChIP2, Kv4.3 and Kv4.2. For KChIP2, there is a positive interaction ( p

    Journal: The Journal of Biological Chemistry

    Article Title: Reductions in the Cardiac Transient Outward K+ Current Ito Caused by Chronic β-Adrenergic Receptor Stimulation Are Partly Rescued by Inhibition of Nuclear Factor κB *

    doi: 10.1074/jbc.M115.694984

    Figure Lengend Snippet: NF-κB inhibition partly reverses decreases in I to,f caused by chronic β-AR stimulation. IkBαSA (adenovirally infected) was used to inhibit NF-κB signaling. A , representative current I to,f current traces. B , averaged I to,f current densities at +60 mV for GFP, GFP+ISO, IkBαSA and IkBαSA+ISO. C , relative mRNA expression for KChIP2, Kv4.3 and Kv4.2. For KChIP2, there is a positive interaction ( p

    Article Snippet: For GAPDH detection, blots for Kv4.2 and KChIP2 were first stripped using commercial stripping buffer (ST010, GeBa) according to manufacturer's instructions.

    Techniques: Inhibition, Infection, Expressing

    Chronic β-AR stimulation and calcineurin inhibition with CAIN. Adenoviral infection with CAIN was used to inhibit calcineurin. A , representative current I to,f current traces. B , averaged I to,f densities (pA/pF) at +60 mV for GFP, GFP+ISO, CAIN and CAIN+ISO. C , relative mRNA expression for KChIP2, Kv4.3 and Kv4.2. **, p

    Journal: The Journal of Biological Chemistry

    Article Title: Reductions in the Cardiac Transient Outward K+ Current Ito Caused by Chronic β-Adrenergic Receptor Stimulation Are Partly Rescued by Inhibition of Nuclear Factor κB *

    doi: 10.1074/jbc.M115.694984

    Figure Lengend Snippet: Chronic β-AR stimulation and calcineurin inhibition with CAIN. Adenoviral infection with CAIN was used to inhibit calcineurin. A , representative current I to,f current traces. B , averaged I to,f densities (pA/pF) at +60 mV for GFP, GFP+ISO, CAIN and CAIN+ISO. C , relative mRNA expression for KChIP2, Kv4.3 and Kv4.2. **, p

    Article Snippet: For GAPDH detection, blots for Kv4.2 and KChIP2 were first stripped using commercial stripping buffer (ST010, GeBa) according to manufacturer's instructions.

    Techniques: Inhibition, Infection, Expressing

    Blockade of phosphorylation at the PKC sites increases the surface expression of Kv4.2 channels in COS-7 cells

    Journal: The Biochemical journal

    Article Title: Kv4.2 is a locus for PKC and ERK/MAPK cross-talk

    doi: 10.1042/BJ20081213

    Figure Lengend Snippet: Blockade of phosphorylation at the PKC sites increases the surface expression of Kv4.2 channels in COS-7 cells

    Article Snippet: Previous data suggest that filamin is a scaffold protein that links Kv4.2 and the actin cytoskeleton.

    Techniques: Expressing

    PKC phosphorylates the Kv4.2 C-terminal but not the N-terminal cytoplasmic domains in vitro

    Journal: The Biochemical journal

    Article Title: Kv4.2 is a locus for PKC and ERK/MAPK cross-talk

    doi: 10.1042/BJ20081213

    Figure Lengend Snippet: PKC phosphorylates the Kv4.2 C-terminal but not the N-terminal cytoplasmic domains in vitro

    Article Snippet: Previous data suggest that filamin is a scaffold protein that links Kv4.2 and the actin cytoskeleton.

    Techniques: In Vitro

    Generation and characterization of the Kv4.2 phospho-specific antibodies for the Ser447 and Ser537 site

    Journal: The Biochemical journal

    Article Title: Kv4.2 is a locus for PKC and ERK/MAPK cross-talk

    doi: 10.1042/BJ20081213

    Figure Lengend Snippet: Generation and characterization of the Kv4.2 phospho-specific antibodies for the Ser447 and Ser537 site

    Article Snippet: Previous data suggest that filamin is a scaffold protein that links Kv4.2 and the actin cytoskeleton.

    Techniques:

    PKC phosphorylation of the Kv4.2 C-terminal augments ERK phosphorylation of the Kv4.2 C-terminal in vitro

    Journal: The Biochemical journal

    Article Title: Kv4.2 is a locus for PKC and ERK/MAPK cross-talk

    doi: 10.1042/BJ20081213

    Figure Lengend Snippet: PKC phosphorylation of the Kv4.2 C-terminal augments ERK phosphorylation of the Kv4.2 C-terminal in vitro

    Article Snippet: Previous data suggest that filamin is a scaffold protein that links Kv4.2 and the actin cytoskeleton.

    Techniques: In Vitro

    Functional characterization of PKC sites within Kv4.2

    Journal: The Biochemical journal

    Article Title: Kv4.2 is a locus for PKC and ERK/MAPK cross-talk

    doi: 10.1042/BJ20081213

    Figure Lengend Snippet: Functional characterization of PKC sites within Kv4.2

    Article Snippet: Previous data suggest that filamin is a scaffold protein that links Kv4.2 and the actin cytoskeleton.

    Techniques: Functional Assay

    Candidate PKC consensus sites within the Kv4.2 channel subunit

    Journal: The Biochemical journal

    Article Title: Kv4.2 is a locus for PKC and ERK/MAPK cross-talk

    doi: 10.1042/BJ20081213

    Figure Lengend Snippet: Candidate PKC consensus sites within the Kv4.2 channel subunit

    Article Snippet: Previous data suggest that filamin is a scaffold protein that links Kv4.2 and the actin cytoskeleton.

    Techniques: