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except ibtx  (Biosynth Carbosynth)


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    Biosynth Carbosynth except ibtx
    EM and IK are similar in resistance PASMCs from wild-type and CGD mice (A) Resting EM is similar in wild-type (filled bar) and CGD (empty bar) PASMCs. (B) Normoxic current density is similar in wild-type and CGD PASMCs. (C and D) In PASMCs from CGD mice, 4-AP, a Kv channel inhibitor, reduces IK at negative potentials (−10 mV, C, ∗, P < 0.05). Tetraethylammonium (TEA) inhibits IK only at positive potentials, where KCa channels are active (∗, P < 0.05, D). (E and F) Four minutes of acute hypoxia inhibits IK (n = 4 cells/group, ∗, P < 0.01). (G and H) In separate experiments, 4 min of acute hypoxia inhibits IK even after specifically inhibiting large conductance KCa channels with <t>IBTX.</t> This finding suggests the hypoxia-sensitive current is at least partially Kv current (†, ∗ P < 0.05 <t>IBTX</t> and hypoxia inhibit IK, respectively).
    Except Ibtx, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 90/100, based on 38 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/except+ibtx/pmc00022167-190-5-7?v=Biosynth+Carbosynth
    Average 90 stars, based on 38 article reviews
    except ibtx - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "O 2 sensing is preserved in mice lacking the gp91 phox subunit of NADPH oxidase"

    Article Title: O 2 sensing is preserved in mice lacking the gp91 phox subunit of NADPH oxidase

    Journal:

    doi:

    EM and IK are similar in resistance PASMCs from wild-type and CGD mice (A) Resting EM is similar in wild-type (filled bar) and CGD (empty bar) PASMCs. (B) Normoxic current density is similar in wild-type and CGD PASMCs. (C and D) In PASMCs from CGD mice, 4-AP, a Kv channel inhibitor, reduces IK at negative potentials (−10 mV, C, ∗, P < 0.05). Tetraethylammonium (TEA) inhibits IK only at positive potentials, where KCa channels are active (∗, P < 0.05, D). (E and F) Four minutes of acute hypoxia inhibits IK (n = 4 cells/group, ∗, P < 0.01). (G and H) In separate experiments, 4 min of acute hypoxia inhibits IK even after specifically inhibiting large conductance KCa channels with IBTX. This finding suggests the hypoxia-sensitive current is at least partially Kv current (†, ∗ P < 0.05 IBTX and hypoxia inhibit IK, respectively).
    Figure Legend Snippet: EM and IK are similar in resistance PASMCs from wild-type and CGD mice (A) Resting EM is similar in wild-type (filled bar) and CGD (empty bar) PASMCs. (B) Normoxic current density is similar in wild-type and CGD PASMCs. (C and D) In PASMCs from CGD mice, 4-AP, a Kv channel inhibitor, reduces IK at negative potentials (−10 mV, C, ∗, P < 0.05). Tetraethylammonium (TEA) inhibits IK only at positive potentials, where KCa channels are active (∗, P < 0.05, D). (E and F) Four minutes of acute hypoxia inhibits IK (n = 4 cells/group, ∗, P < 0.01). (G and H) In separate experiments, 4 min of acute hypoxia inhibits IK even after specifically inhibiting large conductance KCa channels with IBTX. This finding suggests the hypoxia-sensitive current is at least partially Kv current (†, ∗ P < 0.05 IBTX and hypoxia inhibit IK, respectively).

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    FIG. 5. Relative volume measurements in response to 4-PDD in cystic fibrosis airway epithelial cells. A, cell volume changes in CFT1 cells exposed to hypotonic conditions in the absence (, n 12) or presence of 1 M 4-PDD (●, n 13). B, cell volume changes in CFT1 cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 12) or in the presence of 100 mM Gd3 (‚, n 9). C, cell volume changes in CFT1 cells exposed to 1 M 4-PDD and 100 nM clotrimazole (n 12). D, cell volume changes in CFBE cells exposed to 1 M 4-PDD (n 9). E, cell volume changes in CFBE cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 10) or in the presence of 100 mM Gd3 (‚, n 6). F, cell volume changes in CFBE cells exposed to 1 M 4-PDD and 100 nM <t>iberiotoxin</t> (n 7).
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    FIG. 5. Relative volume measurements in response to 4-PDD in cystic fibrosis airway epithelial cells. A, cell volume changes in CFT1 cells exposed to hypotonic conditions in the absence (, n 12) or presence of 1 M 4-PDD (●, n 13). B, cell volume changes in CFT1 cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 12) or in the presence of 100 mM Gd3 (‚, n 9). C, cell volume changes in CFT1 cells exposed to 1 M 4-PDD and 100 nM clotrimazole (n 12). D, cell volume changes in CFBE cells exposed to 1 M 4-PDD (n 9). E, cell volume changes in CFBE cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 10) or in the presence of 100 mM Gd3 (‚, n 6). F, cell volume changes in CFBE cells exposed to 1 M 4-PDD and 100 nM <t>iberiotoxin</t> (n 7).
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    FIG. 5. Relative volume measurements in response to 4-PDD in cystic fibrosis airway epithelial cells. A, cell volume changes in CFT1 cells exposed to hypotonic conditions in the absence (, n 12) or presence of 1 M 4-PDD (●, n 13). B, cell volume changes in CFT1 cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 12) or in the presence of 100 mM Gd3 (‚, n 9). C, cell volume changes in CFT1 cells exposed to 1 M 4-PDD and 100 nM clotrimazole (n 12). D, cell volume changes in CFBE cells exposed to 1 M 4-PDD (n 9). E, cell volume changes in CFBE cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 10) or in the presence of 100 mM Gd3 (‚, n 6). F, cell volume changes in CFBE cells exposed to 1 M 4-PDD and 100 nM <t>iberiotoxin</t> (n 7).
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    Biosynth Carbosynth except ibtx
    EM and IK are similar in resistance PASMCs from wild-type and CGD mice (A) Resting EM is similar in wild-type (filled bar) and CGD (empty bar) PASMCs. (B) Normoxic current density is similar in wild-type and CGD PASMCs. (C and D) In PASMCs from CGD mice, 4-AP, a Kv channel inhibitor, reduces IK at negative potentials (−10 mV, C, ∗, P < 0.05). Tetraethylammonium (TEA) inhibits IK only at positive potentials, where KCa channels are active (∗, P < 0.05, D). (E and F) Four minutes of acute hypoxia inhibits IK (n = 4 cells/group, ∗, P < 0.01). (G and H) In separate experiments, 4 min of acute hypoxia inhibits IK even after specifically inhibiting large conductance KCa channels with <t>IBTX.</t> This finding suggests the hypoxia-sensitive current is at least partially Kv current (†, ∗ P < 0.05 <t>IBTX</t> and hypoxia inhibit IK, respectively).
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    FIG. 5. Relative volume measurements in response to 4-PDD in cystic fibrosis airway epithelial cells. A, cell volume changes in CFT1 cells exposed to hypotonic conditions in the absence (, n 12) or presence of 1 M 4-PDD (●, n 13). B, cell volume changes in CFT1 cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 12) or in the presence of 100 mM Gd3 (‚, n 9). C, cell volume changes in CFT1 cells exposed to 1 M 4-PDD and 100 nM clotrimazole (n 12). D, cell volume changes in CFBE cells exposed to 1 M 4-PDD (n 9). E, cell volume changes in CFBE cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 10) or in the presence of 100 mM Gd3 (‚, n 6). F, cell volume changes in CFBE cells exposed to 1 M 4-PDD and 100 nM iberiotoxin (n 7).

    Journal: Journal of Biological Chemistry

    Article Title: Swelling-activated Ca2+ Entry via TRPV4 Channel Is Defective in Cystic Fibrosis Airway Epithelia

    doi: 10.1074/jbc.m409708200

    Figure Lengend Snippet: FIG. 5. Relative volume measurements in response to 4-PDD in cystic fibrosis airway epithelial cells. A, cell volume changes in CFT1 cells exposed to hypotonic conditions in the absence (, n 12) or presence of 1 M 4-PDD (●, n 13). B, cell volume changes in CFT1 cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 12) or in the presence of 100 mM Gd3 (‚, n 9). C, cell volume changes in CFT1 cells exposed to 1 M 4-PDD and 100 nM clotrimazole (n 12). D, cell volume changes in CFBE cells exposed to 1 M 4-PDD (n 9). E, cell volume changes in CFBE cells exposed to hypotonic solutions containing 1 M 4-PDD in the absence of extracellular Ca2 (●, n 10) or in the presence of 100 mM Gd3 (‚, n 6). F, cell volume changes in CFBE cells exposed to 1 M 4-PDD and 100 nM iberiotoxin (n 7).

    Article Snippet: All chemicals were purchased from SigmaAldrich except iberiotoxin (Alomone Laboratories, Jerusalem, Israel).

    Techniques:

    EM and IK are similar in resistance PASMCs from wild-type and CGD mice (A) Resting EM is similar in wild-type (filled bar) and CGD (empty bar) PASMCs. (B) Normoxic current density is similar in wild-type and CGD PASMCs. (C and D) In PASMCs from CGD mice, 4-AP, a Kv channel inhibitor, reduces IK at negative potentials (−10 mV, C, ∗, P < 0.05). Tetraethylammonium (TEA) inhibits IK only at positive potentials, where KCa channels are active (∗, P < 0.05, D). (E and F) Four minutes of acute hypoxia inhibits IK (n = 4 cells/group, ∗, P < 0.01). (G and H) In separate experiments, 4 min of acute hypoxia inhibits IK even after specifically inhibiting large conductance KCa channels with IBTX. This finding suggests the hypoxia-sensitive current is at least partially Kv current (†, ∗ P < 0.05 IBTX and hypoxia inhibit IK, respectively).

    Journal:

    Article Title: O 2 sensing is preserved in mice lacking the gp91 phox subunit of NADPH oxidase

    doi:

    Figure Lengend Snippet: EM and IK are similar in resistance PASMCs from wild-type and CGD mice (A) Resting EM is similar in wild-type (filled bar) and CGD (empty bar) PASMCs. (B) Normoxic current density is similar in wild-type and CGD PASMCs. (C and D) In PASMCs from CGD mice, 4-AP, a Kv channel inhibitor, reduces IK at negative potentials (−10 mV, C, ∗, P < 0.05). Tetraethylammonium (TEA) inhibits IK only at positive potentials, where KCa channels are active (∗, P < 0.05, D). (E and F) Four minutes of acute hypoxia inhibits IK (n = 4 cells/group, ∗, P < 0.01). (G and H) In separate experiments, 4 min of acute hypoxia inhibits IK even after specifically inhibiting large conductance KCa channels with IBTX. This finding suggests the hypoxia-sensitive current is at least partially Kv current (†, ∗ P < 0.05 IBTX and hypoxia inhibit IK, respectively).

    Article Snippet: All drugs were from Sigma except IBTX (Peptides International) and DPI (Research Biochemicals, Natick, MA).

    Techniques: