Structured Review

Santa Cruz Biotechnology kchip2
Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, <t>KChIP2,</t> and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Kchip2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/kchip2/product/Santa Cruz Biotechnology
Average 86 stars, based on 11 article reviews
Price from $9.99 to $1999.99
kchip2 - by Bioz Stars, 2022-11
86/100 stars

Images

1) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

2) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

3) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

4) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

5) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

6) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

7) Product Images from "Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system"

Article Title: Regulation of Kv4 channel expression in failing rat heart by the thioredoxin system

Journal: American Journal of Physiology. Heart and Circulatory Physiology

doi: 10.1152/ajpheart.91446.2007

Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P
Figure Legend Snippet: Upregulation of K + channel protein by Pyr. A : representative examples of Western blots of Kv4.2, Kv4.3, KChIP2, and Kv1.5 protein in suspensions of isolated myocytes from post-MI and sham-operated hearts. B : mean densitometric measurements of channel subunits are expressed relative to GAPDH. * P

Techniques Used: Western Blot, Isolation

Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P
Figure Legend Snippet: Upregulation of K + channel expression by Pyr. A : mRNA levels of Kv4.2, Kv4.3, and KChIP2 in isolated myocytes from post-MI (black bars) and sham-operated hearts were measured by real-time PCR. Mean data for the post-MI group are expressed relative to sham. * P

Techniques Used: Expressing, Isolation, Real-time Polymerase Chain Reaction

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    Santa Cruz Biotechnology k channel interacting protein 2 kchip2
    Transient outward K + channel expression in transgenic atrial myocytes. Experimental animals involved wild‐type mice (WT) and transgenic mice (TG) expressing the repressor isoform of cyclic adenosine monophosphate response element modulator, CREM‐IbΔC‐X, and were distributed according to age in 6‐week‐old (WT 6w and TG 6w ) and 12‐week‐old (WT 12w and TG 12w ) groups. A , Representative transient outward K + current (I to ) traces recorded as −40 mV sensitive currents from atrial cardiomyocytes of WT 12w and TG 12w . For clarity, current density (expressed in picoamperes/picofarads [pA/pF]) traces from −40 mV with +20 mV increments are displayed. B , Mean±SE of current–voltage plots of the peak current density (I to ). For WT 6w , n/N are 41/15, for TG 6w n/N are 22/14, for WT 12w n/N are 35/19, and for TG 12w n/N are 20/16. Ca through d , Representative immunoblots and quantification of protein expression of calsequestrin (CSQ; Ca ) normalized to Ponceau and of K + voltage‐gated channel subfamily D member 2 (Kv4.2, Cb ) and 3 (Kv4.3, Cc ), and K + channel interacting <t>protein</t> 2 (KChIP2) ( Cd ) normalized to CSQ. Data show mean±SE of N=7 mice per group, except for Kv4.3, where N=6 as the result of an undetectable band in TG 12w . * P
    K Channel Interacting Protein 2 Kchip2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 80/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/k channel interacting protein 2 kchip2/product/Santa Cruz Biotechnology
    Average 80 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    k channel interacting protein 2 kchip2 - by Bioz Stars, 2022-11
    80/100 stars
      Buy from Supplier

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    Santa Cruz Biotechnology kchip2
    Transient outward K + channel expression in transgenic atrial myocytes. Experimental animals involved wild‐type mice (WT) and transgenic mice (TG) expressing the repressor isoform of cyclic adenosine monophosphate response element modulator, CREM‐IbΔC‐X, and were distributed according to age in 6‐week‐old (WT 6w and TG 6w ) and 12‐week‐old (WT 12w and TG 12w ) groups. A , Representative transient outward K + current (I to ) traces recorded as −40 mV sensitive currents from atrial cardiomyocytes of WT 12w and TG 12w . For clarity, current density (expressed in picoamperes/picofarads [pA/pF]) traces from −40 mV with +20 mV increments are displayed. B , Mean±SE of current–voltage plots of the peak current density (I to ). For WT 6w , n/N are 41/15, for TG 6w n/N are 22/14, for WT 12w n/N are 35/19, and for TG 12w n/N are 20/16. Ca through d , Representative immunoblots and quantification of protein expression of calsequestrin (CSQ; Ca ) normalized to Ponceau and of K + voltage‐gated channel subfamily D member 2 (Kv4.2, Cb ) and 3 (Kv4.3, Cc ), and K + channel interacting <t>protein</t> 2 (KChIP2) ( Cd ) normalized to CSQ. Data show mean±SE of N=7 mice per group, except for Kv4.3, where N=6 as the result of an undetectable band in TG 12w . * P
    Kchip2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kchip2/product/Santa Cruz Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kchip2 - by Bioz Stars, 2022-11
    86/100 stars
      Buy from Supplier

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    Transient outward K + channel expression in transgenic atrial myocytes. Experimental animals involved wild‐type mice (WT) and transgenic mice (TG) expressing the repressor isoform of cyclic adenosine monophosphate response element modulator, CREM‐IbΔC‐X, and were distributed according to age in 6‐week‐old (WT 6w and TG 6w ) and 12‐week‐old (WT 12w and TG 12w ) groups. A , Representative transient outward K + current (I to ) traces recorded as −40 mV sensitive currents from atrial cardiomyocytes of WT 12w and TG 12w . For clarity, current density (expressed in picoamperes/picofarads [pA/pF]) traces from −40 mV with +20 mV increments are displayed. B , Mean±SE of current–voltage plots of the peak current density (I to ). For WT 6w , n/N are 41/15, for TG 6w n/N are 22/14, for WT 12w n/N are 35/19, and for TG 12w n/N are 20/16. Ca through d , Representative immunoblots and quantification of protein expression of calsequestrin (CSQ; Ca ) normalized to Ponceau and of K + voltage‐gated channel subfamily D member 2 (Kv4.2, Cb ) and 3 (Kv4.3, Cc ), and K + channel interacting protein 2 (KChIP2) ( Cd ) normalized to CSQ. Data show mean±SE of N=7 mice per group, except for Kv4.3, where N=6 as the result of an undetectable band in TG 12w . * P

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

    Article Title: Inward Rectifier K+ Currents Contribute to the Proarrhythmic Electrical Phenotype of Atria Overexpressing Cyclic Adenosine Monophosphate Response Element Modulator Isoform CREM‐IbΔC‐X

    doi: 10.1161/JAHA.119.016144

    Figure Lengend Snippet: Transient outward K + channel expression in transgenic atrial myocytes. Experimental animals involved wild‐type mice (WT) and transgenic mice (TG) expressing the repressor isoform of cyclic adenosine monophosphate response element modulator, CREM‐IbΔC‐X, and were distributed according to age in 6‐week‐old (WT 6w and TG 6w ) and 12‐week‐old (WT 12w and TG 12w ) groups. A , Representative transient outward K + current (I to ) traces recorded as −40 mV sensitive currents from atrial cardiomyocytes of WT 12w and TG 12w . For clarity, current density (expressed in picoamperes/picofarads [pA/pF]) traces from −40 mV with +20 mV increments are displayed. B , Mean±SE of current–voltage plots of the peak current density (I to ). For WT 6w , n/N are 41/15, for TG 6w n/N are 22/14, for WT 12w n/N are 35/19, and for TG 12w n/N are 20/16. Ca through d , Representative immunoblots and quantification of protein expression of calsequestrin (CSQ; Ca ) normalized to Ponceau and of K + voltage‐gated channel subfamily D member 2 (Kv4.2, Cb ) and 3 (Kv4.3, Cc ), and K + channel interacting protein 2 (KChIP2) ( Cd ) normalized to CSQ. Data show mean±SE of N=7 mice per group, except for Kv4.3, where N=6 as the result of an undetectable band in TG 12w . * P

    Article Snippet: The following rabbit polyclonal primary antibodies were used against K + voltage‐gated channels (Kv) subunits Kv4.2 (1:200, APC 023, Alomone Labs, Jerusalem, Israel), Kv4.3 (1:200, APC 017, Alomone Labs), K + channel interacting protein 2 (KChIP2) (1:200, sc‐25685, Santa Cruz Biotechnology Inc, Santa Cruz, CA), and K + inwardly rectifying channel (Kir) subunits Kir2.1 (1:200, APC 159, Alomone Labs), Kir2.3 (1:1000, APC 032, Alomone Labs), Kir3.1 (1:200, APC 005, Alomone Labs), Kir3.4 (1:200, APC 027, Alomone Labs), and as loading control calsequestrin (1:2500, PA1‐913, Thermo Fisher Scientific).

    Techniques: Expressing, Transgenic Assay, Mouse Assay, Western Blot