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human hcn2  (Alomone Labs)


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    Structured Review

    Alomone Labs human hcn2
    Human Hcn2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 260 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+hcn2/human/10__1113_slash_jp288673-207-20-24
    Average 96 stars, based on 260 article reviews
    human hcn2 - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Sequencing:

    Article Title: HCN1 and HCN2 Proteins Are Expressed in Cochlear Hair Cells
    Article Snippet: Semi-thin sections were examined with a Zeiss EM 900 electron microscope. .. Primary antibodies included a rabbit polyclonal raised to rat HCN1 amino terminus, aa 6–24 (APC-056, Alomone; 1:25), and a rabbit polyclonal raised to amino acids 147–161 of human HCN2, identical to rat HCN2 sequence (APC-030, Alomone; 1:200). .. The secondary antibody was 10 nm gold-conjugated goat anti-rabbit IgG (G3779, Sigma) at 1:50.

    Article Title: HCN1 and HCN2 Proteins Are Expressed in Cochlear Hair Cells
    Article Snippet: .. Primary antibodies included a rabbit polyclonal raised to rat HCN1 amino terminus, aa 6–24 (APC-056, Alomone; 1:25), and a rabbit polyclonal raised to amino acids 147– 161 of human HCN2, identical to rat HCN2 sequence (APC030, Alomone; 1:200). .. The secondary antibody was 10 nm 37630 JOURNAL OF BIOLOGICAL CHEMISTRY VOLUME 287 • NUMBER 45 • NOVEMBER 2, 2012 at M cM aster U niversity on M arch 4, 2015 http://w w w .jbc.org/ D ow nloaded from gold-conjugated goat anti-rabbit IgG (G3779, Sigma) at 1:50.

    Western Blot:

    Article Title: Proteolytic Processing of HCN2 and Co-assembly with HCN4 in the Generation of Cardiac Pacemaker Channels
    Article Snippet: .. Immunoblots and Immunoprecipitations Polyclonal anti-peptide antibodies, generated against N-terminal residues in human HCN2 (residues 147–161) and HCN4 (residues 119–155) were obtained from Alomone Labs, Ltd. (Jerusalem). ..

    Generated:

    Article Title: Proteolytic Processing of HCN2 and Co-assembly with HCN4 in the Generation of Cardiac Pacemaker Channels
    Article Snippet: .. Immunoblots and Immunoprecipitations Polyclonal anti-peptide antibodies, generated against N-terminal residues in human HCN2 (residues 147–161) and HCN4 (residues 119–155) were obtained from Alomone Labs, Ltd. (Jerusalem). ..



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    a , b Representative phasor plots showing FRET between L10-CFP and hHCN2-YFP expressed in small DRG neurons before and after 10 nM paclitaxel treatment. c Summary data of the effects of the β-CD and paclitaxel on the FRET between L10-CFP and hHCN2-YFP. Data shown are mean ± s.e.m., n = 7 for control and β-CD conditions, n = 8 for paclitaxel conditions, ** p = 1e-6 for β-CD and ** p = 4e-6 for paclitaxel compared with the control. One-way ANOVA (no adjustment) was used. d Cartoon showing the design of the FRET sites in the VSD of human <t>HCN2</t> channels and the representative phasor plot showing FRET between donor AF-488 labeled to the HCN2-L323TAG site and the FRET acceptor AF-555 labeled to the HCN2-T240TAA site. e Representative phasor plot of the same FRET pair as in panel ( d ) following acute 5 mM β-cyclodextrin treatment. f Summary data of the effect of the β-CD on the FRET efficiency of hHCN2-L323TAG/T240TAA channels. Data shown are mean ± s.e.m., n = 5 cells for the control and n = 4 cells after β-CD, ** p = 0.002 using two-sided student’s t -test. g Representative phasor plot of the same FRET pair as in panels ( d ) and ( e ), following acute 5 mM β-cyclodextrin treatment with 120 mM KCl in the bath. h Summary data of the effect of the β-CD on the FRET efficiency as shown in panel ( g ). Data shown are mean ± s.e.m., n = 7 cells for the control and n = 6 cells with β-CD, p = 0.054 using two-sided student’s t -test.
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    Image Search Results


    a , b Representative phasor plots showing FRET between L10-CFP and hHCN2-YFP expressed in small DRG neurons before and after 10 nM paclitaxel treatment. c Summary data of the effects of the β-CD and paclitaxel on the FRET between L10-CFP and hHCN2-YFP. Data shown are mean ± s.e.m., n = 7 for control and β-CD conditions, n = 8 for paclitaxel conditions, ** p = 1e-6 for β-CD and ** p = 4e-6 for paclitaxel compared with the control. One-way ANOVA (no adjustment) was used. d Cartoon showing the design of the FRET sites in the VSD of human HCN2 channels and the representative phasor plot showing FRET between donor AF-488 labeled to the HCN2-L323TAG site and the FRET acceptor AF-555 labeled to the HCN2-T240TAA site. e Representative phasor plot of the same FRET pair as in panel ( d ) following acute 5 mM β-cyclodextrin treatment. f Summary data of the effect of the β-CD on the FRET efficiency of hHCN2-L323TAG/T240TAA channels. Data shown are mean ± s.e.m., n = 5 cells for the control and n = 4 cells after β-CD, ** p = 0.002 using two-sided student’s t -test. g Representative phasor plot of the same FRET pair as in panels ( d ) and ( e ), following acute 5 mM β-cyclodextrin treatment with 120 mM KCl in the bath. h Summary data of the effect of the β-CD on the FRET efficiency as shown in panel ( g ). Data shown are mean ± s.e.m., n = 7 cells for the control and n = 6 cells with β-CD, p = 0.054 using two-sided student’s t -test.

    Journal: Nature Communications

    Article Title: Membrane lipid nanodomains modulate HCN pacemaker channels in nociceptor DRG neurons

    doi: 10.1038/s41467-024-54053-z

    Figure Lengend Snippet: a , b Representative phasor plots showing FRET between L10-CFP and hHCN2-YFP expressed in small DRG neurons before and after 10 nM paclitaxel treatment. c Summary data of the effects of the β-CD and paclitaxel on the FRET between L10-CFP and hHCN2-YFP. Data shown are mean ± s.e.m., n = 7 for control and β-CD conditions, n = 8 for paclitaxel conditions, ** p = 1e-6 for β-CD and ** p = 4e-6 for paclitaxel compared with the control. One-way ANOVA (no adjustment) was used. d Cartoon showing the design of the FRET sites in the VSD of human HCN2 channels and the representative phasor plot showing FRET between donor AF-488 labeled to the HCN2-L323TAG site and the FRET acceptor AF-555 labeled to the HCN2-T240TAA site. e Representative phasor plot of the same FRET pair as in panel ( d ) following acute 5 mM β-cyclodextrin treatment. f Summary data of the effect of the β-CD on the FRET efficiency of hHCN2-L323TAG/T240TAA channels. Data shown are mean ± s.e.m., n = 5 cells for the control and n = 4 cells after β-CD, ** p = 0.002 using two-sided student’s t -test. g Representative phasor plot of the same FRET pair as in panels ( d ) and ( e ), following acute 5 mM β-cyclodextrin treatment with 120 mM KCl in the bath. h Summary data of the effect of the β-CD on the FRET efficiency as shown in panel ( g ). Data shown are mean ± s.e.m., n = 7 cells for the control and n = 6 cells with β-CD, p = 0.054 using two-sided student’s t -test.

    Article Snippet: Wild-type human HCN2 construct was synthesized by VectorBuilder (Chicago, IL).

    Techniques: Control, Labeling

    qPCR data evaluating the expression of key Purkinje markers in control and PURK-cocktail-treated cells The PURK-cocktail treatment induced a different genetic profile, which resembled closely to that of native cardiac Purkinje cells on both AC16-CM and iPSC-CM compared to the control. Data corresponds to mean ± SEM of n=3. ∗,∗∗,∗∗∗,∗∗∗∗ corresponds to p < 0.05, 0.01, 0.001, and 0.0001 in a two-Way ANOVA test. “ns” corresponds to “not significant.”

    Journal: iScience

    Article Title: Direct reprogramming of cardiomyocytes into cardiac Purkinje-like cells

    doi: 10.1016/j.isci.2022.105402

    Figure Lengend Snippet: qPCR data evaluating the expression of key Purkinje markers in control and PURK-cocktail-treated cells The PURK-cocktail treatment induced a different genetic profile, which resembled closely to that of native cardiac Purkinje cells on both AC16-CM and iPSC-CM compared to the control. Data corresponds to mean ± SEM of n=3. ∗,∗∗,∗∗∗,∗∗∗∗ corresponds to p < 0.05, 0.01, 0.001, and 0.0001 in a two-Way ANOVA test. “ns” corresponds to “not significant.”

    Article Snippet: HCN2 Human qPCR Primer Pair , OriGene , cat# HP205124.

    Techniques: Expressing, Control

    Journal: iScience

    Article Title: Direct reprogramming of cardiomyocytes into cardiac Purkinje-like cells

    doi: 10.1016/j.isci.2022.105402

    Figure Lengend Snippet:

    Article Snippet: HCN2 Human qPCR Primer Pair , OriGene , cat# HP205124.

    Techniques: Recombinant, Transfection, Knock-Out, Multiplex sample analysis, SYBR Green Assay, Reverse Transcription, Derivative Assay, Plasmid Preparation, Software

     qPCR  program

    Journal: iScience

    Article Title: Direct reprogramming of cardiomyocytes into cardiac Purkinje-like cells

    doi: 10.1016/j.isci.2022.105402

    Figure Lengend Snippet: qPCR program

    Article Snippet: HCN2 Human qPCR Primer Pair , OriGene , cat# HP205124.

    Techniques: Activation Assay

    Journal: iScience

    Article Title: Direct reprogramming of cardiomyocytes into cardiac Purkinje-like cells

    doi: 10.1016/j.isci.2022.105402

    Figure Lengend Snippet:

    Article Snippet: HCN2 Human qPCR Primer Pair , OriGene , cat# HP205124.

    Techniques: Recombinant, Transfection, Knock-Out, SYBR Green Assay, Derivative Assay, Plasmid Preparation, Software