dtx k Search Results


dtx k  (Alomone Labs)
94
Alomone Labs dtx k
Kv1.1 containing K + channels regulate the excitability of CC-Parv neurons. (A) Summary plot of V rest (left): resting membrane potential; R in (right): input resistance; recorded from layer 5 CC-Parv neurons before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if <t>DTX-KI,</t> including group averages (± S.E.M.). (B) Same as in panel (A) , for AP half width. (C) Summary plot of Rheobase (left), and AP threshold (right); recorded from layer 5 CC-Parv neurons pre- (red circles, n = 7; animals n = 5) and post- (green circles, n = 7; animals n = 5) <t>DTX-K,</t> including group averages (± S.E.M.). (D) Summary plot of averaging firing rate per current step amplitude in response to increasing depolarizing current (0–500 pA, 50 pA increments) recorded from layer 5 CC-Parv before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.). (E) Summary plot of instantaneous firing frequency in response to increasing depolarizing current (300–500 pA, 50 pA increments) for layer 5 CC-Parv before (red circles, n = 10; animals n = 5) and after (Green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.); * p < 0.05.
Dtx K, 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/product/dtx+k/Dendrotoxin-K/pmc05845545-54-19-24
Average 94 stars, based on 1 article reviews
dtx k - by Bioz Stars, 2026-10
94/100 stars
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dtx-k  (CH Instruments)
90
CH Instruments dtx-k
Kv1.1 containing K + channels regulate the excitability of CC-Parv neurons. (A) Summary plot of V rest (left): resting membrane potential; R in (right): input resistance; recorded from layer 5 CC-Parv neurons before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if <t>DTX-KI,</t> including group averages (± S.E.M.). (B) Same as in panel (A) , for AP half width. (C) Summary plot of Rheobase (left), and AP threshold (right); recorded from layer 5 CC-Parv neurons pre- (red circles, n = 7; animals n = 5) and post- (green circles, n = 7; animals n = 5) <t>DTX-K,</t> including group averages (± S.E.M.). (D) Summary plot of averaging firing rate per current step amplitude in response to increasing depolarizing current (0–500 pA, 50 pA increments) recorded from layer 5 CC-Parv before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.). (E) Summary plot of instantaneous firing frequency in response to increasing depolarizing current (300–500 pA, 50 pA increments) for layer 5 CC-Parv before (red circles, n = 10; animals n = 5) and after (Green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.); * p < 0.05.
Dtx K, supplied by CH Instruments, 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/product/dtx+k/dtx+k/pm26609114-167-5-21
Average 90 stars, based on 1 article reviews
dtx-k - by Bioz Stars, 2026-10
90/100 stars
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pcdna3.1-dtxk-lumitoxin (plasmid #51691)  (Addgene inc)
N/A
Standard format: Plasmid sent in bacteria as agar stab
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Image Search Results


Kv1.1 containing K + channels regulate the excitability of CC-Parv neurons. (A) Summary plot of V rest (left): resting membrane potential; R in (right): input resistance; recorded from layer 5 CC-Parv neurons before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if DTX-KI, including group averages (± S.E.M.). (B) Same as in panel (A) , for AP half width. (C) Summary plot of Rheobase (left), and AP threshold (right); recorded from layer 5 CC-Parv neurons pre- (red circles, n = 7; animals n = 5) and post- (green circles, n = 7; animals n = 5) DTX-K, including group averages (± S.E.M.). (D) Summary plot of averaging firing rate per current step amplitude in response to increasing depolarizing current (0–500 pA, 50 pA increments) recorded from layer 5 CC-Parv before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.). (E) Summary plot of instantaneous firing frequency in response to increasing depolarizing current (300–500 pA, 50 pA increments) for layer 5 CC-Parv before (red circles, n = 10; animals n = 5) and after (Green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.); * p < 0.05.

Journal: Frontiers in Cellular Neuroscience

Article Title: Layer 5 Callosal Parvalbumin-Expressing Neurons: A Distinct Functional Group of GABAergic Neurons

doi: 10.3389/fncel.2018.00053

Figure Lengend Snippet: Kv1.1 containing K + channels regulate the excitability of CC-Parv neurons. (A) Summary plot of V rest (left): resting membrane potential; R in (right): input resistance; recorded from layer 5 CC-Parv neurons before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if DTX-KI, including group averages (± S.E.M.). (B) Same as in panel (A) , for AP half width. (C) Summary plot of Rheobase (left), and AP threshold (right); recorded from layer 5 CC-Parv neurons pre- (red circles, n = 7; animals n = 5) and post- (green circles, n = 7; animals n = 5) DTX-K, including group averages (± S.E.M.). (D) Summary plot of averaging firing rate per current step amplitude in response to increasing depolarizing current (0–500 pA, 50 pA increments) recorded from layer 5 CC-Parv before (red circles, n = 7; animals n = 5) and after (green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.). (E) Summary plot of instantaneous firing frequency in response to increasing depolarizing current (300–500 pA, 50 pA increments) for layer 5 CC-Parv before (red circles, n = 10; animals n = 5) and after (Green circles, n = 7; animals n = 5) bath application if DTX-K, including group averages (± S.E.M.); * p < 0.05.

Article Snippet: The pharmacological blockers used were CPP (5 μM, Tocris), NBQX (10 μM, Abcam), gabazine (10 μM, Abcam), DTX-I and DTX-K (50 and 100 nM, Alomone labs).

Techniques: Membrane, Patch Clamp

Kv1.1 containing K + channels shape layer 5 CC-Parv neurons firing. (A) Example responses to a 20 Hz train of 5 EPSC-like waveforms (top) recorded from layer 5 CC-Parv neuron before (red trace), and after (green trace) bath application of DTX-K. Layer 5 CC-Parv neurons show increased firing after bath application of DTX-K (green trace). (B) Average plot of AP responses to a train of EPSC-like waveforms before (red bars), and after (green bars) bath application of DTX-K, including group averages (± S.E.M.); * p < 0.05.

Journal: Frontiers in Cellular Neuroscience

Article Title: Layer 5 Callosal Parvalbumin-Expressing Neurons: A Distinct Functional Group of GABAergic Neurons

doi: 10.3389/fncel.2018.00053

Figure Lengend Snippet: Kv1.1 containing K + channels shape layer 5 CC-Parv neurons firing. (A) Example responses to a 20 Hz train of 5 EPSC-like waveforms (top) recorded from layer 5 CC-Parv neuron before (red trace), and after (green trace) bath application of DTX-K. Layer 5 CC-Parv neurons show increased firing after bath application of DTX-K (green trace). (B) Average plot of AP responses to a train of EPSC-like waveforms before (red bars), and after (green bars) bath application of DTX-K, including group averages (± S.E.M.); * p < 0.05.

Article Snippet: The pharmacological blockers used were CPP (5 μM, Tocris), NBQX (10 μM, Abcam), gabazine (10 μM, Abcam), DTX-I and DTX-K (50 and 100 nM, Alomone labs).

Techniques: Patch Clamp