anti-trpc4 antibody Search Results


mouse trpc4  (Alomone Labs)
93
Alomone Labs mouse trpc4
Functional expression of transient receptor potential canonical (TRPC) channels in mouse ventricular myocytes. (A–C) Activation of TRPC current by thapsigargin recorded under conditions where Na+, Ca2+ and K+ channel currents were minimized. (A) Time course of changes in membrane current measured at +50 and −110 mV during the voltage-ramp protocol (from +50 to −110 mV), before and during exposure to thapsigargin (Thap, 2 µmol·L−1), without and then with 2-APB (20 µmol·L−1). (B) I-V relationships measured at time points (a, b, c) indicated in (A). (C) Difference currents obtained by digital subtraction as indicated (b-a: thapsigargin-activated current; b-c: 2-APB-sensitive current). (D) Immunostaining of TRPC1, TRPC3 and <t>TRPC4.</t> Scale bar in all panels, 25 µm.
Mouse Trpc4, 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/mouse trpc4/product/Alomone Labs
Average 93 stars, based on 1 article reviews
mouse trpc4 - by Bioz Stars, 2026-02
93/100 stars
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anti-trpc4 antibody  (Antibodies Inc)
90
Antibodies Inc anti-trpc4 antibody
Functional expression of transient receptor potential canonical (TRPC) channels in mouse ventricular myocytes. (A–C) Activation of TRPC current by thapsigargin recorded under conditions where Na+, Ca2+ and K+ channel currents were minimized. (A) Time course of changes in membrane current measured at +50 and −110 mV during the voltage-ramp protocol (from +50 to −110 mV), before and during exposure to thapsigargin (Thap, 2 µmol·L−1), without and then with 2-APB (20 µmol·L−1). (B) I-V relationships measured at time points (a, b, c) indicated in (A). (C) Difference currents obtained by digital subtraction as indicated (b-a: thapsigargin-activated current; b-c: 2-APB-sensitive current). (D) Immunostaining of TRPC1, TRPC3 and <t>TRPC4.</t> Scale bar in all panels, 25 µm.
Anti Trpc4 Antibody, supplied by Antibodies Inc, 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/anti-trpc4 antibody/product/Antibodies Inc
Average 90 stars, based on 1 article reviews
anti-trpc4 antibody - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier
polyclonal rabbit anti trpc4 antibody acc 119 against amino acids 458 469  (Alomone Labs)
91
Alomone Labs polyclonal rabbit anti trpc4 antibody acc 119 against amino acids 458 469
Functional expression of transient receptor potential canonical (TRPC) channels in mouse ventricular myocytes. (A–C) Activation of TRPC current by thapsigargin recorded under conditions where Na+, Ca2+ and K+ channel currents were minimized. (A) Time course of changes in membrane current measured at +50 and −110 mV during the voltage-ramp protocol (from +50 to −110 mV), before and during exposure to thapsigargin (Thap, 2 µmol·L−1), without and then with 2-APB (20 µmol·L−1). (B) I-V relationships measured at time points (a, b, c) indicated in (A). (C) Difference currents obtained by digital subtraction as indicated (b-a: thapsigargin-activated current; b-c: 2-APB-sensitive current). (D) Immunostaining of TRPC1, TRPC3 and <t>TRPC4.</t> Scale bar in all panels, 25 µm.
Polyclonal Rabbit Anti Trpc4 Antibody Acc 119 Against Amino Acids 458 469, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal rabbit anti trpc4 antibody acc 119 against amino acids 458 469/product/Alomone Labs
Average 91 stars, based on 1 article reviews
polyclonal rabbit anti trpc4 antibody acc 119 against amino acids 458 469 - by Bioz Stars, 2026-02
91/100 stars
  Buy from Supplier
trpc4  (Boster Bio)
90
Boster Bio trpc4
Functional expression of transient receptor potential canonical (TRPC) channels in mouse ventricular myocytes. (A–C) Activation of TRPC current by thapsigargin recorded under conditions where Na+, Ca2+ and K+ channel currents were minimized. (A) Time course of changes in membrane current measured at +50 and −110 mV during the voltage-ramp protocol (from +50 to −110 mV), before and during exposure to thapsigargin (Thap, 2 µmol·L−1), without and then with 2-APB (20 µmol·L−1). (B) I-V relationships measured at time points (a, b, c) indicated in (A). (C) Difference currents obtained by digital subtraction as indicated (b-a: thapsigargin-activated current; b-c: 2-APB-sensitive current). (D) Immunostaining of TRPC1, TRPC3 and <t>TRPC4.</t> Scale bar in all panels, 25 µm.
Trpc4, supplied by Boster Bio, 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/trpc4/product/Boster Bio
Average 90 stars, based on 1 article reviews
trpc4 - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

Image Search Results


Functional expression of transient receptor potential canonical (TRPC) channels in mouse ventricular myocytes. (A–C) Activation of TRPC current by thapsigargin recorded under conditions where Na+, Ca2+ and K+ channel currents were minimized. (A) Time course of changes in membrane current measured at +50 and −110 mV during the voltage-ramp protocol (from +50 to −110 mV), before and during exposure to thapsigargin (Thap, 2 µmol·L−1), without and then with 2-APB (20 µmol·L−1). (B) I-V relationships measured at time points (a, b, c) indicated in (A). (C) Difference currents obtained by digital subtraction as indicated (b-a: thapsigargin-activated current; b-c: 2-APB-sensitive current). (D) Immunostaining of TRPC1, TRPC3 and TRPC4. Scale bar in all panels, 25 µm.

Journal: British Journal of Pharmacology

Article Title: Ca 2+ paradox injury mediated through TRPC channels in mouse ventricular myocytes

doi: 10.1111/j.1476-5381.2010.00986.x

Figure Lengend Snippet: Functional expression of transient receptor potential canonical (TRPC) channels in mouse ventricular myocytes. (A–C) Activation of TRPC current by thapsigargin recorded under conditions where Na+, Ca2+ and K+ channel currents were minimized. (A) Time course of changes in membrane current measured at +50 and −110 mV during the voltage-ramp protocol (from +50 to −110 mV), before and during exposure to thapsigargin (Thap, 2 µmol·L−1), without and then with 2-APB (20 µmol·L−1). (B) I-V relationships measured at time points (a, b, c) indicated in (A). (C) Difference currents obtained by digital subtraction as indicated (b-a: thapsigargin-activated current; b-c: 2-APB-sensitive current). (D) Immunostaining of TRPC1, TRPC3 and TRPC4. Scale bar in all panels, 25 µm.

Article Snippet: Rabbit anti-TRPC1 antibody directed against an extracellular epitope of human TRPC1 (ACC-010), rabbit anti-TRPC3 antibody directed against an intracellular C-terminal epitope of mouse TRPC3 (ACC-016), rabbit anti-TRPC4 antibody directed against an intracellular C-terminal epitope of mouse TRPC4 (ACC-018), rabbit anti-TRPC5 antibody directed against an intracellular epitope of human TRPC5 (ACC-020) were from Alomone Laboratories (Jerusalem, Israel), and normal rabbit IgG was from Santa Cruz Biotechnology (Santa Cruz, CA, USA).

Techniques: Functional Assay, Expressing, Activation Assay, Immunostaining