antiphospho smad1 5 9 antibody Search Results


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Cell Signaling Technology Inc anti phospho smad1 5 9 antibody
Anti Phospho Smad1 5 9 Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Millipore phospho-smad1/5/9
Expression of <t>pSMAD1/5/9</t> in fibroblasts of FOP patients and controls by western blotting analysis. ( A ) Cells were serum-starved overnight before 60 min of stimulation with Activin A and ( B ) serum-starved overnight before 90 min of stimulation with BMP4. Actin was used to determine equal protein loading. −FBS are serum-starved unstimulated fibroblasts.
Phospho Smad1/5/9, supplied by Millipore, 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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Cell Signaling Technology Inc anti phospho smad1 5 9
Expression of <t>pSMAD1/5/9</t> in fibroblasts of FOP patients and controls by western blotting analysis. ( A ) Cells were serum-starved overnight before 60 min of stimulation with Activin A and ( B ) serum-starved overnight before 90 min of stimulation with BMP4. Actin was used to determine equal protein loading. −FBS are serum-starved unstimulated fibroblasts.
Anti Phospho Smad1 5 9, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti phospho smad1 5 9/product/Cell Signaling Technology Inc
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Cell Signaling Technology Inc anti-phospho-smad
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
Anti Phospho Smad, supplied by Cell Signaling Technology 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-phospho-smad/product/Cell Signaling Technology Inc
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anti-phospho-smad - by Bioz Stars, 2026-02
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Cell Signaling Technology Inc anti-phospho-smad1/5/9
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
Anti Phospho Smad1/5/9, supplied by Cell Signaling Technology 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-phospho-smad1/5/9/product/Cell Signaling Technology Inc
Average 90 stars, based on 1 article reviews
anti-phospho-smad1/5/9 - by Bioz Stars, 2026-02
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Millipore anti-phospho-smad1/5/9 antibody ab3848-i
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
Anti Phospho Smad1/5/9 Antibody Ab3848 I, supplied by Millipore, 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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Cell Signaling Technology Inc rabbit anti phospho smad1 5 9
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
Rabbit Anti Phospho Smad1 5 9, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc anti phospho smads
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
Anti Phospho Smads, supplied by Cell Signaling Technology Inc, 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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New England Biolabs anti phospho smad 5 antibodies
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
Anti Phospho Smad 5 Antibodies, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc o c anti phospho smad1 5 9 d5b10 rabbit mab
a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP <t>receptor,</t> <t>Smad1</t> and <t>phospho-SMAD</t> expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.
O C Anti Phospho Smad1 5 9 D5b10 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Expression of pSMAD1/5/9 in fibroblasts of FOP patients and controls by western blotting analysis. ( A ) Cells were serum-starved overnight before 60 min of stimulation with Activin A and ( B ) serum-starved overnight before 90 min of stimulation with BMP4. Actin was used to determine equal protein loading. −FBS are serum-starved unstimulated fibroblasts.

Journal: International Journal of Molecular Sciences

Article Title: TGF-Beta Induces Activin A Production in Dermal Fibroblasts Derived from Patients with Fibrodysplasia Ossificans Progressiva

doi: 10.3390/ijms24032299

Figure Lengend Snippet: Expression of pSMAD1/5/9 in fibroblasts of FOP patients and controls by western blotting analysis. ( A ) Cells were serum-starved overnight before 60 min of stimulation with Activin A and ( B ) serum-starved overnight before 90 min of stimulation with BMP4. Actin was used to determine equal protein loading. −FBS are serum-starved unstimulated fibroblasts.

Article Snippet: Primary antibodies against phospho-SMAD3 (cat#52903, Abcam), phospho-SMAD1/5/9 (AB3848-I, Sigma-Aldrich), and Actin (Cat#ab14128, Abcam) were used for overnight incubation.

Techniques: Expressing, Western Blot

a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP receptor, Smad1 and phospho-SMAD expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.

Journal: Nature

Article Title: Brahma safeguards canalization of cardiac mesoderm differentiation

doi: 10.1038/s41586-021-04336-y

Figure Lengend Snippet: a, Dot plots showing quantitative changes in gene expression between WT and Brm−/− cells induced with normal (1x) or high (4x) BMP4 concentrations at D4, D6 and D10 stages of differentiation for early developmental, cardiac mesoderm, precursor, and myocyte genes enriched in BRM KO cells. b-d, Transcriptional trajectory analysis of WT and BRM KO cells showing the genotype representation in normal BMP4 concentration (b), normal BMP4 for WT and 4x BMP4 concentration for BRM KO cells (c) and URD feature plots of expression of Nkx2-;5, and Actc1 (d). e, Western blots showing BMP receptor, Smad1 and phospho-SMAD expression during D0 to D4 of cardiac differentiation, f-g, Scatter plots of single cell RNASeq data showing mean gene expression and variance from mean gene expression at D4 stage of differentiation for WT (f) and Brm−/− cells (g) in low and high BMP4 conditions. h-i, Signaling entropy calculated similarly for WT (h) and Brm−/− cells (i) with low and high BMP4 conditions.

Article Snippet: Primary antibodies used were anti- BRG1 (Abcam, ab110641, 1:1000), anti-BRM (Abcam, ab240648, 1:1000), anti-FLAG (Sigma, F1804, 1:1000), anti-BAF170 (Bethyl, 1:1000, A301–39A), anti-BAF60c (Cell Signaling Technology, 62265, 1:1000), anti-REST (EMD-Millipore, 07–579, 1:1000), anti-POU3F1 (Abcam, ab126746, 1:1000), or anti-TBP (Abcam, ab51841, 1:2000), anti-Vinculin (Sigma-Aldrich V9131, 1:1000), anti-phospho-Smad (CST 9511, 1:1000), and anti-Smad1 (CST 9743, 1:1000).

Techniques: Expressing, Concentration Assay, Western Blot