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cav3 3  (Alomone Labs)
94
Alomone Labs cav3 3
All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and <t>CaV3.1</t> ( d ), CaV3.2 ( e ) <t>and</t> <t>CaV3.3</t> ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).
Cav3 3, 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
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cav3 2  (Alomone Labs)
93
Alomone Labs cav3 2
All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and <t>CaV3.1</t> ( d <t>),</t> <t>CaV3.2</t> ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).
Cav3 2, 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/cav3 2/product/Alomone Labs
Average 93 stars, based on 1 article reviews
cav3 2 - by Bioz Stars, 2026-03
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cav3 1  (Alomone Labs)
93
Alomone Labs cav3 1
All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and <t>CaV3.1</t> ( d <t>),</t> <t>CaV3.2</t> ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).
Cav3 1, 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
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Average 93 stars, based on 1 article reviews
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voltage dependent t type calcium channel subunits cav3 1  (Alomone Labs)
93
Alomone Labs voltage dependent t type calcium channel subunits cav3 1
All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and <t>CaV3.1</t> ( d <t>),</t> <t>CaV3.2</t> ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).
Voltage Dependent T Type Calcium Channel Subunits Cav3 1, 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
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Average 93 stars, based on 1 article reviews
voltage dependent t type calcium channel subunits cav3 1 - by Bioz Stars, 2026-03
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All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and CaV3.1 ( d ), CaV3.2 ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).

Journal: Nature Communications

Article Title: Endothelin-3 and T-type Ca 2+ channels drive enteric neural crest cell calcium activity, contractility and migration

doi: 10.1038/s41467-025-68121-5

Figure Lengend Snippet: All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and CaV3.1 ( d ), CaV3.2 ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).

Article Snippet: After fixation, blocking and permeation, samples were incubated for 1 day in 1:200 mouse Anti-SOX10 and 1:100 rabbit anti CaV3.1 (Alomone Labs #ACC-021) or 1:100 rabbit anti CaV3.2 (Alomone Labs #ACC-025) or 1:100 rabbit anti CaV3.3 (Alomone Labs #ACC-009) for 24 h, washed 3 times, incubated in secondary 1:500 anti-mouse Cy3 and 1:500 anti-rabbit AF647 antibody for another day, washed and imaged.

Techniques: Control, Two Tailed Test

All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and CaV3.1 ( d ), CaV3.2 ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).

Journal: Nature Communications

Article Title: Endothelin-3 and T-type Ca 2+ channels drive enteric neural crest cell calcium activity, contractility and migration

doi: 10.1038/s41467-025-68121-5

Figure Lengend Snippet: All experiments in ( a – c ) are performed at E11.5 at the ileo-cecal junction. Error bars are ±SD. a CA change relative to control before drug application for EDTA (2 mM, n = 6), GdCl3 (100 µM, n = 6), 2-APB (100 µM, n = 5), ryanodine (10 µM, n = 5). b CA change for nifedipine (Nif, 10 µM, n = 5), ruthenium red (RuR, 100 µM, n = 6), Z944 at 1 µM ( n = 7), 10 µM ( n = 7), 50 µM ( n = 9), ascorbic acid (AA, 1 mM, n = 13) and SAK3 at 1 µM ( n = 6), 10 µM ( n = 6). c CA change for NPPB (100 µM, n = 11), NFA (50 µM, n = 9) and DIDS (500 µM, n = 5). Two-tailed p -values for (a-c) are calculated from the Student t-test. Sox10 and CaV3.1 ( d ), CaV3.2 ( e ) and CaV3.3 ( f ) IHCs of ENCCs migrating from an intestinal explant on a substrate. All three T-type Ca 2+ channels are expressed by ENCCs, but not by the surrounding mesenchymal cells. The small bright green dots are AF647 µ-beads fluorescing in the same range as the T-type Ca 2+ channel secondary antibody. They were added in the overlying collagen gel for another experiment (see Fig. ).

Article Snippet: After fixation, blocking and permeation, samples were incubated for 1 day in 1:200 mouse Anti-SOX10 and 1:100 rabbit anti CaV3.1 (Alomone Labs #ACC-021) or 1:100 rabbit anti CaV3.2 (Alomone Labs #ACC-025) or 1:100 rabbit anti CaV3.3 (Alomone Labs #ACC-009) for 24 h, washed 3 times, incubated in secondary 1:500 anti-mouse Cy3 and 1:500 anti-rabbit AF647 antibody for another day, washed and imaged.

Techniques: Control, Two Tailed Test