bmp6 rabbit polyclonal 685 antibody Search Results


92
R&D Systems mouse anti bmp6
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Santa Cruz Biotechnology primary antibody against bmp6
Fig. 2. <t>BMP6</t> as the candidate target gene ofmiR- 124-3p in cells with the ‘seed sequence’ in the 3’UTR.
Primary Antibody Against Bmp6, supplied by Santa Cruz Biotechnology, 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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R&D Systems recombinant human bmp6 protein
Fig. 2. <t>BMP6</t> as the candidate target gene ofmiR- 124-3p in cells with the ‘seed sequence’ in the 3’UTR.
Recombinant Human Bmp6 Protein, supplied by R&D Systems, 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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Proteintech bmp6 polyclonal antibody
The combinations of transfected plasmids
Bmp6 Polyclonal Antibody, supplied by Proteintech, 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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R&D Systems human bmp6
The combinations of transfected plasmids
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R&D Systems recombinant human bmp6
<t>BMP6</t> upregulates the expression of CTGF in hGL cells. A and B, SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blotting, respectively. C and D, SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CTGF were examined using RT-qPCR and western blotting, respectively. E and F, Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CTGF were examined using RT-qPCR and Western blot, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). B6, BMP6; Ctrl, control; hGL, primary human granulosa lutein.
Recombinant Human Bmp6, supplied by R&D Systems, 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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Novus Biologicals bmp6
Antibodies used in the study
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ImmunoWay Biotechnology Company rabbit anti-bmp6
Antibodies used in the study
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Santa Cruz Biotechnology goat anti bmp6
Antibodies used in the study
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Santa Cruz Biotechnology bmp6
Antibodies used in the study
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R&D Systems anti human bmp 6 antibody
Antibodies used in the study
Anti Human Bmp 6 Antibody, supplied by R&D Systems, 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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R&D Systems bmp6
Antibodies used in the study
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Image Search Results


Fig. 2. BMP6 as the candidate target gene ofmiR- 124-3p in cells with the ‘seed sequence’ in the 3’UTR.

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.

doi: 10.1159/000475570

Figure Lengend Snippet: Fig. 2. BMP6 as the candidate target gene ofmiR- 124-3p in cells with the ‘seed sequence’ in the 3’UTR.

Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min. primary antibody against BMP6 (1:1,000; Santa Cruz Biotechnology, Beijing, China) was used to hybridize the membranes at 4°C for 12 hours.

Techniques: Sequencing

Fig. 4. The correlation between the expression level of miR-124-3p and BMP6 mRNA.

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.

doi: 10.1159/000475570

Figure Lengend Snippet: Fig. 4. The correlation between the expression level of miR-124-3p and BMP6 mRNA.

Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min. primary antibody against BMP6 (1:1,000; Santa Cruz Biotechnology, Beijing, China) was used to hybridize the membranes at 4°C for 12 hours.

Techniques: Expressing

Fig. 5. The expression of BMP6 mRNA (Fig. 5A) and protein (Fig. 5B) decreased in GG group compared with GC and CC group (** P<0.01 compared with the control).

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.

doi: 10.1159/000475570

Figure Lengend Snippet: Fig. 5. The expression of BMP6 mRNA (Fig. 5A) and protein (Fig. 5B) decreased in GG group compared with GC and CC group (** P<0.01 compared with the control).

Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min. primary antibody against BMP6 (1:1,000; Santa Cruz Biotechnology, Beijing, China) was used to hybridize the membranes at 4°C for 12 hours.

Techniques: Expressing, Control

Fig. 3. Luciferase activity reporter assay was conducted to verify BMP6 as the direct target gene of miR-124-3p (** P<0.01 compared with the control).

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Article Title: A MicroRNA-124 Polymorphism is Associated with Fracture Healing via Modulating BMP6 Expression.

doi: 10.1159/000475570

Figure Lengend Snippet: Fig. 3. Luciferase activity reporter assay was conducted to verify BMP6 as the direct target gene of miR-124-3p (** P<0.01 compared with the control).

Article Snippet: TBST containing 5% non-fat dry milk (Merck, Darmstadt, Germany) was used to block the membranes for 60 min. primary antibody against BMP6 (1:1,000; Santa Cruz Biotechnology, Beijing, China) was used to hybridize the membranes at 4°C for 12 hours.

Techniques: Luciferase, Activity Assay, Reporter Assay, Control

The combinations of transfected plasmids

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: The combinations of transfected plasmids

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques: Transfection, Plasmid Preparation

Primers used for quantitative real-time polymerase chain reaction

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: Primers used for quantitative real-time polymerase chain reaction

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques: Sequencing

Antibody information

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: Antibody information

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques:

Comparison of the expression levels of BMAL1 and BMP6 in human OGCs between PCOS and control groups. A, B BMAL1 and BMP6 mRNA levels between PCOS and control groups. C–E BMAL1 and BMP6 protein levels between PCOS and control groups. F Correlations between the mRNA expression levels of BMP6 and BMAL1 in OGCs. * P < 0.05, ** P < 0.01, and *** P < 0.001

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: Comparison of the expression levels of BMAL1 and BMP6 in human OGCs between PCOS and control groups. A, B BMAL1 and BMP6 mRNA levels between PCOS and control groups. C–E BMAL1 and BMP6 protein levels between PCOS and control groups. F Correlations between the mRNA expression levels of BMP6 and BMAL1 in OGCs. * P < 0.05, ** P < 0.01, and *** P < 0.001

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques: Comparison, Expressing, Control

The mRNA levels of BMAL1 and BMP6 in OGCs are correlated with ART outcomes of patients. Spearman’s correlation analyses were used to investigate the correlation between the mRNA levels of BMAL1 and the number of retrieved oocytes ( A ), 2PN fertilized oocytes ( B ), available embryos ( C ), and high-quality embryos ( D ). Spearman’s correlation analyses were used to investigate the correlation between the mRNA levels of BMP6 and the number of retrieved oocytes ( E ), 2PN fertilized oocytes ( F ), available embryos ( G ), and high-quality embryos ( H )

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: The mRNA levels of BMAL1 and BMP6 in OGCs are correlated with ART outcomes of patients. Spearman’s correlation analyses were used to investigate the correlation between the mRNA levels of BMAL1 and the number of retrieved oocytes ( A ), 2PN fertilized oocytes ( B ), available embryos ( C ), and high-quality embryos ( D ). Spearman’s correlation analyses were used to investigate the correlation between the mRNA levels of BMP6 and the number of retrieved oocytes ( E ), 2PN fertilized oocytes ( F ), available embryos ( G ), and high-quality embryos ( H )

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques:

BMP6 is a downstream target of BMAL1. A Predicted binding site and mutated binding site of BMAL1 in the promoter of BMP6[created with figdraw.com]. B Direct interaction between BMAL1 and BMP6 detected by the dual-luciferase assay. * P < 0.05, ** P < 0.01, and *** P < 0.001

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: BMP6 is a downstream target of BMAL1. A Predicted binding site and mutated binding site of BMAL1 in the promoter of BMP6[created with figdraw.com]. B Direct interaction between BMAL1 and BMP6 detected by the dual-luciferase assay. * P < 0.05, ** P < 0.01, and *** P < 0.001

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques: Binding Assay, Luciferase

The impact of BMAL1 on the expression of BMP6 in KGN cells. A, B Expression levels of BMAL1 and BMP6 mRNA in KGN cells after transfection. C, D Expression levels of BMP6 protein in KGN cells after transfection. OE, overexpression; NC, negative control. * P < 0.05, ** P < 0.01, and *** P < 0.001

Journal: Journal of Assisted Reproduction and Genetics

Article Title: BMAL1 improves assisted reproductive technology outcomes in patients with polycystic ovary syndrome by targeting BMP6 and regulating ovarian granulosa cell apoptosis

doi: 10.1007/s10815-024-03377-2

Figure Lengend Snippet: The impact of BMAL1 on the expression of BMP6 in KGN cells. A, B Expression levels of BMAL1 and BMP6 mRNA in KGN cells after transfection. C, D Expression levels of BMP6 protein in KGN cells after transfection. OE, overexpression; NC, negative control. * P < 0.05, ** P < 0.01, and *** P < 0.001

Article Snippet: BMP6 Polyclonal antibody , 55,421–1-AP , Proteintech , 1:1000.

Techniques: Expressing, Transfection, Over Expression, Negative Control

BMP6 upregulates the expression of CTGF in hGL cells. A and B, SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blotting, respectively. C and D, SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CTGF were examined using RT-qPCR and western blotting, respectively. E and F, Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CTGF were examined using RT-qPCR and Western blot, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). B6, BMP6; Ctrl, control; hGL, primary human granulosa lutein.

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: BMP6 upregulates the expression of CTGF in hGL cells. A and B, SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blotting, respectively. C and D, SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CTGF were examined using RT-qPCR and western blotting, respectively. E and F, Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CTGF were examined using RT-qPCR and Western blot, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). B6, BMP6; Ctrl, control; hGL, primary human granulosa lutein.

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Expressing, Quantitative RT-PCR, Western Blot

BMP6 does not affect the expression of CYR61 in hGL cells. (A and B) SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. (C and D) SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. (E and F) Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: BMP6 does not affect the expression of CYR61 in hGL cells. (A and B) SVOG cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (A) or 6 h (B), and the mRNA (A) and protein (B) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. (C and D) SVOG cells were treated with vehicle control or 30 ng/ml of BMP6 for 1, 3, 6, 12, or 24 h, and the mRNA (C) and protein (D) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. (E and F) Primary hGL cells were treated with a vehicle control or increasing concentrations (5, 20, or 100 ng/ml) of BMP6 for 3 h (E) or 6 h (F), and the mRNA (E) and protein (F) levels of CYR61 were examined using RT-qPCR and western blotting, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Expressing, Quantitative RT-PCR, Western Blot

BMP6 induces the phosphorylation of SMAD1/5/8 in SVOG cells. (A) SVOG cells were treated with a vehicle control or 30 ng/ml of BMP6 for 20, 40, or 60 min, and the phosphorylated protein levels of SMAD1/5/8 were examined using western blotting. (B) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 40 min. The phosphorylated protein levels of SMAD1/5/8 were examined using western blotting. (C) SVOG cells were treated with a vehicle control or 30 ng/ml BMP6 for 40 min, fixed in 4% paraformaldehyde in PBS, and examined for phosphorylated SMAD1/5/8 (red) and nuclear (DAPI in blue) immunofluorescence. (D) SVOG cells were treated with a vehicle control, 30 ng/ml of BMP6 (for 20, 40, or 60 min) or 5 ng/ml of TGF-β1 (for 20 min as a positive control) and the phosphorylated protein levels of SMAD2 and SMAD3 were examined using western blotting. (E) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 40 min. The phosphorylated protein levels of SMAD2 and SMAD3 were examined using western blotting. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: BMP6 induces the phosphorylation of SMAD1/5/8 in SVOG cells. (A) SVOG cells were treated with a vehicle control or 30 ng/ml of BMP6 for 20, 40, or 60 min, and the phosphorylated protein levels of SMAD1/5/8 were examined using western blotting. (B) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 40 min. The phosphorylated protein levels of SMAD1/5/8 were examined using western blotting. (C) SVOG cells were treated with a vehicle control or 30 ng/ml BMP6 for 40 min, fixed in 4% paraformaldehyde in PBS, and examined for phosphorylated SMAD1/5/8 (red) and nuclear (DAPI in blue) immunofluorescence. (D) SVOG cells were treated with a vehicle control, 30 ng/ml of BMP6 (for 20, 40, or 60 min) or 5 ng/ml of TGF-β1 (for 20 min as a positive control) and the phosphorylated protein levels of SMAD2 and SMAD3 were examined using western blotting. (E) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 40 min. The phosphorylated protein levels of SMAD2 and SMAD3 were examined using western blotting. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Western Blot, Immunofluorescence, Positive Control

ALK2 or ALK3 is required for the BMP6-induced upregulation of CTGF expression in SVOG cells. (A and B) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 3 h (A) and 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blot, respectively. (C and D) SVOG cells were pretreated with a vehicle control (DMSO) or 5 μM SB431542 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 3 h (C) and 6 h (D), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blot, respectively. (E and F) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl), 25 nM of ALK2 siRNA (siALK2), 25 nM of ALK3 siRNA (siALK3), or 25 nM of siALK2 combined with 25 nM of siALK3, followed by treatment with vehicle control or 30 ng/ml of BMP6 for 40 min (E) and 3 h (F). The phosphorylated protein levels of SMAD1/5/8 (E) and mRNA levels of CTGF were examined using western blotting and RT-qPCR, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). ALK, activin receptor-like kinase.

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: ALK2 or ALK3 is required for the BMP6-induced upregulation of CTGF expression in SVOG cells. (A and B) SVOG cells were pretreated with a vehicle control (DMSO), 5 μM dorsomorphin, or 5 μM DMH-1 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 3 h (A) and 6 h (B), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blot, respectively. (C and D) SVOG cells were pretreated with a vehicle control (DMSO) or 5 μM SB431542 for 60 min, and then treated with 30 ng/ml BMP6 for an additional 3 h (C) and 6 h (D), and the mRNA (A) and protein (B) levels of CTGF were examined using RT-qPCR and western blot, respectively. (E and F) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl), 25 nM of ALK2 siRNA (siALK2), 25 nM of ALK3 siRNA (siALK3), or 25 nM of siALK2 combined with 25 nM of siALK3, followed by treatment with vehicle control or 30 ng/ml of BMP6 for 40 min (E) and 3 h (F). The phosphorylated protein levels of SMAD1/5/8 (E) and mRNA levels of CTGF were examined using western blotting and RT-qPCR, respectively. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). ALK, activin receptor-like kinase.

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Expressing, Quantitative RT-PCR, Western Blot, Transfection

SMAD-dependent signaling pathway is required for the BMP6-induced stimulation of CTGF in SVOG cells. (A) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of SMAD4 and CTGF were examined using RT-qPCR. (B) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4) followed by treatment with vehicle control or 30 ng/ml of BMP6 for 6 h. The protein levels of CTGF and SMAD4 were examined using western blotting. (C) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of SMAD4 and CYR61 were examined using RT-qPCR. (D) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4) followed by treatment with vehicle control or 30 ng/ml of BMP6 for 6 h. The protein levels of CYR61 and SMAD4 were examined using western blotting. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: SMAD-dependent signaling pathway is required for the BMP6-induced stimulation of CTGF in SVOG cells. (A) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of SMAD4 and CTGF were examined using RT-qPCR. (B) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4) followed by treatment with vehicle control or 30 ng/ml of BMP6 for 6 h. The protein levels of CTGF and SMAD4 were examined using western blotting. (C) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of SMAD4 and CYR61 were examined using RT-qPCR. (D) SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of SMAD4 siRNA (siSMAD4) followed by treatment with vehicle control or 30 ng/ml of BMP6 for 6 h. The protein levels of CYR61 and SMAD4 were examined using western blotting. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05).

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Transfection, Quantitative RT-PCR, Western Blot

CTGF mediates the BMP6-induced up-regulation of LOX expression in SVOG cells. SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of CTGF siRNA (siCTGF), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of CTGF and LOX were examined using RT-qPCR. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). LOX, lysyl oxidase.

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: CTGF mediates the BMP6-induced up-regulation of LOX expression in SVOG cells. SVOG cells were transfected for 24 h with 25 nM of control siRNA (siCtrl) or 25 nM of CTGF siRNA (siCTGF), followed by treatment with vehicle control or 30 ng/ml of BMP6 for 3 h. The mRNA levels of CTGF and LOX were examined using RT-qPCR. The results are expressed as the mean ± SEM of at least three independent experiments. Values marked by different letters are significantly different (P < 0.05). LOX, lysyl oxidase.

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Expressing, Transfection, Quantitative RT-PCR

Proposed model for the effect of BMP6 on the expression levels CTGF and LOX in human granulosa-lutein cells. BMP6 binds to a complex containing type I (ALK2 and ALK3) and II receptors leading to the phosphorylation/activation of receptor-regulated SMAD (SMAD1/5/8), which binds to the common SMAD (SMAD4). This complex then translocates into the nucleus to promote the transcription of CTGF. The up-regulation of CTGF subsequently contributes to the increase in LOX expression in human granulosa-lutein cells.

Journal: Biology of Reproduction

Article Title: SMAD-dependent signaling mediates morphogenetic protein 6-induced stimulation of connective tissue growth factor in luteinized human granulosa cells

doi: 10.1093/biolre/ioz108

Figure Lengend Snippet: Proposed model for the effect of BMP6 on the expression levels CTGF and LOX in human granulosa-lutein cells. BMP6 binds to a complex containing type I (ALK2 and ALK3) and II receptors leading to the phosphorylation/activation of receptor-regulated SMAD (SMAD1/5/8), which binds to the common SMAD (SMAD4). This complex then translocates into the nucleus to promote the transcription of CTGF. The up-regulation of CTGF subsequently contributes to the increase in LOX expression in human granulosa-lutein cells.

Article Snippet: Antibodies and reagents Recombinant human BMP6 (#507-BP-020), recombinant human TGF-β1 (#240-B-010), dorsomorphin dihydrochloride (dorsomorphin) (#3093/10), DMH-1 (#4126/10), and SB431542 (#1614/10) were obtained from R&D Systems (Minneapolis, MN).

Techniques: Expressing, Activation Assay

Antibodies used in the study

Journal: The EMBO journal

Article Title: Self-organized developmental patterning and differentiation in cerebral organoids

doi: 10.15252/embj.201694700

Figure Lengend Snippet: Antibodies used in the study

Article Snippet: BMP6 , Rabbit , Novus Biologicals , NBP1‐19733 , 1:100.

Techniques: