p q channel  (Alomone Labs)


Bioz Verified Symbol Alomone Labs is a verified supplier
Bioz Manufacturer Symbol Alomone Labs manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 93

    Structured Review

    Alomone Labs p q channel
    P Q Channel, 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/p q channel/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    p q channel - by Bioz Stars, 2022-08
    93/100 stars

    Images

    Similar Products

  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90
    Alomone Labs rabbit anti nk1
    SP stimulates its receptors on Type I cells and induces Ca 2+ release from intracellular stores. (A) Bath‐application of 10 nM SP elicits Ca 2+ mobilization in Fura 2‐loaded taste cells (↓, SP). RP67580 (0.1 μM), an <t>NK1</t> receptor antagonist (present throughout the shaded area), reversibly inhibited SP‐induced Ca 2+ responses. (B) Summary of SP‐elicited Ca 2+ responses before, during and after the presence of RP67580, plotted as in (A). Points represent normalized peak taste cell responses. Blue symbols show mean ± 95% confidence interval (95% CI). * P
    Rabbit Anti Nk1, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti nk1/product/Alomone Labs
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti nk1 - by Bioz Stars, 2022-08
    90/100 stars
      Buy from Supplier

    93
    Alomone Labs penitrem a
    The identification of K + channels in setting HCASMC resting membrane potential. (A–F) The change in the fractional fluorescence of DiBAC 4 (3) treated with 10 µM glibenclamide (A), 200 nM <t>penitrem</t> A (B), 1 µM tram34 (C), 200 nM apamin (D), 25 µM BaCl 2 (E), and 10 µM XE991 (F). (G) A summary of percentchange in fractional fluorescence of DiBAC 4 (3) after application of K + channel inhibitors: glibenclamide ( p
    Penitrem A, 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/penitrem a/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    penitrem a - by Bioz Stars, 2022-08
    93/100 stars
      Buy from Supplier

    95
    Alomone Labs ω agatoxin iva
    Characterization of HVA currents . (A) Example time course response of a neuron exposed to: nifedipine (1 μM), <t>ω-Agatoxin</t> <t>IVA</t> (400 nM) and ω-Conotoxin GVIA (2 μM). Right: Current traces obtained before (a) and after addition of the drugs (b–d) (V T = +10 mV, V H = −50 mV). (B) Percentage block of HVA current by antagonists in WT and KO neurons. (C) Western blot analysis of HVA channel subunits. Top: Examples of protein levels of HVA channel subunits in WT and KO hippocampus. Bottom: Quantification of α 1A , α 1C , α 1D , α 1B protein ratios (KO/WT). * p
    ω Agatoxin Iva, 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
    https://www.bioz.com/result/ω agatoxin iva/product/Alomone Labs
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    ω agatoxin iva - by Bioz Stars, 2022-08
    95/100 stars
      Buy from Supplier

    94
    Alomone Labs vgcc subtypes
    Characterization of HVA currents . (A) Example time course response of a neuron exposed to: nifedipine (1 μM), <t>ω-Agatoxin</t> <t>IVA</t> (400 nM) and ω-Conotoxin GVIA (2 μM). Right: Current traces obtained before (a) and after addition of the drugs (b–d) (V T = +10 mV, V H = −50 mV). (B) Percentage block of HVA current by antagonists in WT and KO neurons. (C) Western blot analysis of HVA channel subunits. Top: Examples of protein levels of HVA channel subunits in WT and KO hippocampus. Bottom: Quantification of α 1A , α 1C , α 1D , α 1B protein ratios (KO/WT). * p
    Vgcc Subtypes, 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/vgcc subtypes/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    vgcc subtypes - by Bioz Stars, 2022-08
    94/100 stars
      Buy from Supplier

    Image Search Results


    SP stimulates its receptors on Type I cells and induces Ca 2+ release from intracellular stores. (A) Bath‐application of 10 nM SP elicits Ca 2+ mobilization in Fura 2‐loaded taste cells (↓, SP). RP67580 (0.1 μM), an NK1 receptor antagonist (present throughout the shaded area), reversibly inhibited SP‐induced Ca 2+ responses. (B) Summary of SP‐elicited Ca 2+ responses before, during and after the presence of RP67580, plotted as in (A). Points represent normalized peak taste cell responses. Blue symbols show mean ± 95% confidence interval (95% CI). * P

    Journal: British Journal of Pharmacology

    Article Title: Substance P as a putative efferent transmitter mediates GABAergic inhibition in mouse taste buds) Substance P as a putative efferent transmitter mediates GABAergic inhibition in mouse taste buds

    doi: 10.1111/bph.14142

    Figure Lengend Snippet: SP stimulates its receptors on Type I cells and induces Ca 2+ release from intracellular stores. (A) Bath‐application of 10 nM SP elicits Ca 2+ mobilization in Fura 2‐loaded taste cells (↓, SP). RP67580 (0.1 μM), an NK1 receptor antagonist (present throughout the shaded area), reversibly inhibited SP‐induced Ca 2+ responses. (B) Summary of SP‐elicited Ca 2+ responses before, during and after the presence of RP67580, plotted as in (A). Points represent normalized peak taste cell responses. Blue symbols show mean ± 95% confidence interval (95% CI). * P

    Article Snippet: We used rabbit anti‐NK1 (1:200; catalogue #ATR‐001; Alomone Labs, Jerusalem, Israel) for NK1 receptors (Muñoz et al., ), guinea pig anti‐GLAST (1:200; catalogue #AB‐2571717; Frontier Institute, Hokkaido, Japan) for Type I cells (Yoshida et al., ) and rabbit anti‐GABA (1:1500; catalogue #A2050; Sigma) for taste cell transmitter (Dvoryanchikov et al., ; Huang et al., ).

    Techniques:

    The identification of K + channels in setting HCASMC resting membrane potential. (A–F) The change in the fractional fluorescence of DiBAC 4 (3) treated with 10 µM glibenclamide (A), 200 nM penitrem A (B), 1 µM tram34 (C), 200 nM apamin (D), 25 µM BaCl 2 (E), and 10 µM XE991 (F). (G) A summary of percentchange in fractional fluorescence of DiBAC 4 (3) after application of K + channel inhibitors: glibenclamide ( p

    Journal: PeerJ

    Article Title: Hypoxia and metabolic inhibitors alter the intracellular ATP:ADP ratio and membrane potential in human coronary artery smooth muscle cells

    doi: 10.7717/peerj.10344

    Figure Lengend Snippet: The identification of K + channels in setting HCASMC resting membrane potential. (A–F) The change in the fractional fluorescence of DiBAC 4 (3) treated with 10 µM glibenclamide (A), 200 nM penitrem A (B), 1 µM tram34 (C), 200 nM apamin (D), 25 µM BaCl 2 (E), and 10 µM XE991 (F). (G) A summary of percentchange in fractional fluorescence of DiBAC 4 (3) after application of K + channel inhibitors: glibenclamide ( p

    Article Snippet: However, exposure to hypoxia resulted in significant decrease in DiBAC4 (3) fluorescence when in the presence of 10 µM pinacidil (n = 5), 10 µM glibenclamide (n = 36), 25 µM BaCl2 (n = 14), 100 nM IbTX (n = 17), 200 nM penitrem A (n = 14), and 10 µM glibenclamide plus 25 µM BaCl2 (n = 25) ( ).

    Techniques: Fluorescence

    Characterization of HVA currents . (A) Example time course response of a neuron exposed to: nifedipine (1 μM), ω-Agatoxin IVA (400 nM) and ω-Conotoxin GVIA (2 μM). Right: Current traces obtained before (a) and after addition of the drugs (b–d) (V T = +10 mV, V H = −50 mV). (B) Percentage block of HVA current by antagonists in WT and KO neurons. (C) Western blot analysis of HVA channel subunits. Top: Examples of protein levels of HVA channel subunits in WT and KO hippocampus. Bottom: Quantification of α 1A , α 1C , α 1D , α 1B protein ratios (KO/WT). * p

    Journal: Frontiers in Cellular Neuroscience

    Article Title: Calcium current homeostasis and synaptic deficits in hippocampal neurons from Kelch-like 1 knockout mice

    doi: 10.3389/fncel.2014.00444

    Figure Lengend Snippet: Characterization of HVA currents . (A) Example time course response of a neuron exposed to: nifedipine (1 μM), ω-Agatoxin IVA (400 nM) and ω-Conotoxin GVIA (2 μM). Right: Current traces obtained before (a) and after addition of the drugs (b–d) (V T = +10 mV, V H = −50 mV). (B) Percentage block of HVA current by antagonists in WT and KO neurons. (C) Western blot analysis of HVA channel subunits. Top: Examples of protein levels of HVA channel subunits in WT and KO hippocampus. Bottom: Quantification of α 1A , α 1C , α 1D , α 1B protein ratios (KO/WT). * p

    Article Snippet: Test pulses were elicited every 8 s. Calcium channel blockers were applied in a sequential manner, 1 μM nifedipine (L-type currents; Sigma, St. Louis, MO), 200 nM ω-Agatoxin IVA (P/Q-type currents; Alomone Labs, Jerusalem, Israel) and 2 μM ω-Conotoxin GVIA (N-type currents; Tocris, Bristol, UK).

    Techniques: Blocking Assay, Western Blot