phalloidin staining Search Results


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VANGL2 LTD phalloidin staining
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
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Becton Dickinson alexa fluor 488® phalloidin actin staining
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
Alexa Fluor 488® Phalloidin Actin Staining, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biozol Diagnostica Vertrieb GmbH acti-stain phalloidin 488
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
Acti Stain Phalloidin 488, supplied by Biozol Diagnostica Vertrieb GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MetaMorph Inc phalloidin-stained images
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
Phalloidin Stained Images, supplied by MetaMorph Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CH Instruments phalloidin for f-actin filament staining
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
Phalloidin For F Actin Filament Staining, 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
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Beijing Solarbio Science anti-stain tm488 fluorescent phalloidin
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
Anti Stain Tm488 Fluorescent Phalloidin, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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universal imaging inc phalloidin stained images
Looptail mutation disrupts actin cytoskeleton regulation. (A-D) <t>Phalloidin</t> staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).
Phalloidin Stained Images, supplied by universal imaging inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Looptail mutation disrupts actin cytoskeleton regulation. (A-D) Phalloidin staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).

Journal: Disease Models & Mechanisms

Article Title: Heterozygous Vangl2 Looptail mice reveal novel roles for the planar cell polarity pathway in adult lung homeostasis and repair

doi: 10.1242/dmm.028175

Figure Lengend Snippet: Looptail mutation disrupts actin cytoskeleton regulation. (A-D) Phalloidin staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice. Student's t -test, P >0.05). (G) p-Cfl levels are significantly reduced in both Vangl2 Lp/+ (70%) and Vangl2 Lp/Lp (57%) lungs compared with WT littermates ( n =6 per genotype; three separate gels were run, with each gel containing one lane of lung lysate from each genotype. Each lane contained pooled lysate from two individual mice; Student's t -test, * P <0.05). (H) Western blot of total β-catenin (92 kDa) in the cell membrane and cytosolic fractions of adult lungs, and β-actin (42 kDa) and Gapdh (37 kDa) loading controls. Quantification of β-catenin levels (I) in the membrane fraction showed 55% reduction in Vangl2 Lp/+ mice compared with WT controls ( n =3 per genotype, with samples run on a single gel, Student's t -test, * P <0.05). (J) No significant difference was found in the cytosolic compartment ( n =3 per genotype, with samples run on a single gel; Student's t -test, P >0.05). (K) Western blot of E-cadherin in the cell membrane fraction of adult lungs, and Gapdh (37 kDa) loading control. (L) Quantification of E-cadherin levels in the membrane fraction shows no significant difference between Vangl2 Lp/+ mice and WT controls ( n =6 per genotype, two separate gels were run, each with lung lysate from three individual mice per genotype; Student's t -test, P >0.05). Scale bars: 25 µm (A,B) and 12.5 µm (C,D).

Article Snippet: Looptail mutation disrupts actin cytoskeleton regulation. (A-D) Phalloidin staining of filamentous actin distribution in (A,C) WT and (B,D) Vangl2 Lp/+ at (A,B) E14.5 and (C,D) E18.5. (E) Western blot of Cfl and p-Cfl (both 19 kDa) and Gapdh (37 kDa) in total protein lysate from E14.5 WT, Vangl2 Lp/+ and Vangl2 Lp/Lp lungs. (F) Quantification of total Cfl in WT, Vangl2 Lp/+ and Vangl2 Lp/Lp littermates, revealed no significant differences (mean±s.e.m., n =6 per genotype; 3 separate gels were run, with each gel containing 1 lane of lung lysate from each genotype.

Techniques: Mutagenesis, Staining, Western Blot, Membrane, Control