lf bmp7 r d systems (R&D Systems)
Structured Review

Lf Bmp7 R D Systems, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lf+bmp7+r+d+systems/pm32693087-256-35-37?v=R%26D+Systems
Average 90 stars, based on 3 article reviews
Images
1) Product Images from "LEFTY1 Is a Dual-SMAD Inhibitor that Promotes Mammary Progenitor Growth and Tumorigenesis."
Article Title: LEFTY1 Is a Dual-SMAD Inhibitor that Promotes Mammary Progenitor Growth and Tumorigenesis.
Journal: Cell stem cell
doi: 10.1016/j.stem.2020.06.017
Figure Legend Snippet: Figure 1. LEFTY1 Expression Is Restricted to a Subset of Luminal Cells and Rare Basal Cells, while BMP7 Is Secreted Predominantly by Basal Cells (A) Left: representative FACS plot of the mouse mammary epithelial cell subpopulations stained with the indicated cell-surface markers. Different subpopulations are indicated as described in the color key. Right: Principal-component analysis reveals different subpopulations based on single-cell PCR analysis. (B) Hierarchically clustered analysis of single-cell PCR analysis of sorted mouse mammary epithelial populations. (C) Representative images of BMP7 protein staining of mammary glands isolated from 6- to 8-week-old WT mice. Scale bar, 20 mm. (D) Representative images of LEFTY1 protein staining of mammary glands isolated from 6- to 8-week-old WT mice. Scale bar, 20 mm. See also Figure S1.
Techniques Used: Expressing, Staining, Isolation
Figure Legend Snippet: Figure 2. LEFTY1 Induces and BMP7 Reduces Ductal Branching and the Long-Term Proliferative Potential of Mammary Progenitor Cells (A) Schematic representation of procedure used to inject ligand-secreting L1 fibroblasts into the mammary fat pad followed by analysis of mammary glands. (B) Quantification of branches counted in glands exposed to the LEFTY1 (n = 6) or control (n = 7) group. Statistical analysis, Student’s t test. ***p < 0.001. Data are represented as mean ± SEM. (C) Quantification of branches counted in glands exposed to the BMP7 (n = 6) or control (n = 7) group. Statistical analysis, Student’s t test. *p < 0.05. Data are represented as mean ± SEM. (D) Representative images of the whole-mount staining of the indicated groups of mice. Magnification, 403. (E) Representative images of the organoids grown in the presence of BMP7, LEFTY1, or control (n = 7). Scale bar, 100 mm.
Techniques Used: Control, Staining
Figure Legend Snippet: Figure 3. LEFTY1 Simultaneously Suppresses SMAD2 and SMAD5 in Basal Cells (A) Quantification of pSMAD2-positive cells within the luminal and basal compartments of endogenous ductal structures exposed to LEFTY1-secreting fibro- blasts. Data are represented as mean ± SD. Statistical analysis, Student’s t test. ****p < 0.0001. (B) Quantification of pSMAD2-positive cells within the luminal and basal compartments of endogenous ductal structures exposed to BMP7-secreting fibroblasts. Data are represented as mean ± SD. Statistical analysis, Student’s t test. n.s., non-significant. (C) Quantification of pSMAD5-positive cells within the luminal and basal compartments of endogenous ductal structures exposed to LEFTY1-secreting fibro- blasts. Data are represented as mean ± SD. Statistical analysis, Student’s t test. *p < 0.05; ****p < 0.0001. (D) Quantification of pSMAD5-positive cells within the luminal and basal compartments of endogenous ductal structures exposed to BMP7-secreting fibroblasts. Data are represented as mean ± SD. Statistical analysis, Student’s t test. *p < 0.05; n.s., non-significant. (E) Representative images of the quantified sections for pSMAD2 analysis of mammary glands exposed to LEFTY1-secreting fibroblasts. (F) Representative images of the quantified sections for pSMAD5 analysis of mammary glands exposed to LEFTY1-secreting fibroblasts. (G) Representative images of the quantified sections for pSMAD2 analysis of mammary glands exposed to BMP7-secreting fibroblasts. (H) Representative images of the quantified sections for pSMAD5 analysis of mammary glands exposed to BMP7-secreting fibroblasts. (I) Western blot for pSMAD2, pSMAD5, total SMAD2/3, or SMAD1/5/8 proteins in COMMA-D cells blocked with LEFTY1 and stimulated with BMP7 and Nodal (n = 3). (J) Quantification of the pSMAD5 signal detected by western blot in the indicated conditions. (K) Quantification of the pSMAD2 signal detected by western blot in the indicated conditions. Scale bar, 20 mm. See also Figure S5.
Techniques Used: Western Blot
Figure Legend Snippet: Figure 4. LEFTY1 Directly Binds to the BMP Receptor BMPR2 (A) Relative mRNA levels of Bmpr2 in basal cell populations (CD49fhiCD24med and CD49flowCD24low) and luminal ones (CD49flowCD24hi and CD49flow/-CD24med). Statistical analysis is one-way ANOVA with Dunnett’s adjustment. (B) Representative images of proximity ligation assay show the interaction between LEFTY1 and BMPR2. Red puncta indicate positive interactions. Scale bar, 10 mm. (C) Quantification of the positive interaction between BMP7 or LEFTY1 with BMPR2 (n = 3). Statistical analysis is one-way ANOVA with Dunnett’s adjustment. ****p < 0.0001. (D) Western blot on co-immunoprecipitated beads of LEFTY1 and BMPR2. (E) Schematic representation of the mechanism by which LEFTY1 inhibits SMAD5 and SMAD2 phosphorylation. See also Figure S5.
Techniques Used: Proximity Ligation Assay, Western Blot, Immunoprecipitation, Phospho-proteomics
Figure Legend Snippet: Figure 7. LEFTY1 Binds to BMPR2 and Is a Concomitant SMAD2 and SMAD5 Inhibitor in Tumor-Initiating Cells (A) Representative pictures of cells from isolated tumorigenic (TG) and non-TG (NTG) cells to assess LEFTY1-BMPR2 and BMP7-BMRP2 interaction. Scale bar, 20 mm. (B) Quantification by proximity ligation assay of LEFTY1-BMPR2 or BMP7-BMPR2 interaction in TG cells or NTG sorted cells. (C) Representative images of cells from isolated TG and NTG cells stained to assess pSMAD5 staining. Scale bar, 100 mm.
Techniques Used: Isolation, Proximity Ligation Assay, Staining