mouse pdgf r beta antibody Search Results


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R&D Systems goat anti pdgfrβ
FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Goat Anti Pdgfrβ, supplied by R&D Systems, 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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FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Rat Mouse Pdgf β, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems rabbit anti pdgfr β antibody
FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Rabbit Anti Pdgfr β 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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Bioworld Antibodies mouse monoclonal antibodies against pdgfb pdgfr β
FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Mouse Monoclonal Antibodies Against Pdgfb Pdgfr β, supplied by Bioworld Antibodies, 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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Becton Dickinson mouse antihuman pdgfr β monoclonal primary antibody
FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Mouse Antihuman Pdgfr β Monoclonal Primary Antibody, 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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Bio-Techne corporation human pdgf r beta antibody
FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Human Pdgf R Beta Antibody, supplied by Bio-Techne corporation, 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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Bio-Techne corporation human/mouse phospho-pdgf r beta (y751) antibody
FIGURE 3 <t>PDGFRβ-positive</t> pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin <t>B4</t> <t>(IB4,</t> blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm
Human/Mouse Phospho Pdgf R Beta (Y751) Antibody, supplied by Bio-Techne corporation, 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


FIGURE 3 PDGFRβ-positive pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin B4 (IB4, blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm

Journal: The FASEB Journal

Article Title: Pericyte dynamics in the mouse germinal matrix angiogenesis

doi: 10.1096/fj.202200120r

Figure Lengend Snippet: FIGURE 3 PDGFRβ-positive pericyte coverage is similar between the mouse GM and the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin B4 (IB4, blue), and for pericytes (anti-PDGFRβ, red). Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Yellow asterisk indicates IB4 labeled macrophages at E10.5 in the CTX. Cropped individual images (white solid boxes) of the endothelium and PDGFRβ-positive pericytes are displayed below each timepoint to best visualize pericyte coverage of the blood vessels (A′,B′). (C) Example of data and method used to quantify pericyte coverage (see Materials and Methods). (D) Quantification of pericyte coverage reveals no significant differences between the CTX and the GM. Scatter dot plot shows mean values with standard deviation n = 5 per time point except E10.5 (n = 4) and P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm

Article Snippet: Samples were then immunostained in PBLEC (5% Triton X- 100, 1 M MgCl2, 1 M CaCl2, and 1 M MnCl2 in 1X PBS) overnight at 4°C with Biotinylated IB4 (1:50; Vector Laboratories; Cat# BAF1042) and/or the following antibodies: goat anti- PDGFRβ (1:100; R&D Systems; Cat# BAF1042), rabbit anti- NG2 (1:700; Millipore; Cat# AB5320), rabbit anti- Desmin (1:500; Abcam; Cat# AB15200), anti– αSMA- FITC (1:200; Millipore Sigma, Cat# F3777).

Techniques: Staining, Labeling, Standard Deviation, Comparison

FIGURE 4 Delayed NG2 expression in pericytes of the mouse GM compared to the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin B4 (IB4, blue) and for pericytes with anti-PDGFRβ (red) and anti-NG2.63 Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Cropped individual images (white solid boxes) of the endothelium and pericytes are displayed below each timepoint to best visualize the overlap of NG2 and PDGFRβ expression and pericyte coverage of the blood vessels (A′,B′). Note that in the CTX and the GM/SVZ, NG2 is also expressed by oligodendrocyte precursor cells beginning at E14.5; these cells were excluded from the analysis. (C) Quantification of NG2-positive pericyte coverage reveals reduced coverage at E11.5 in the GM. Scatter dot plot shows mean values with standard deviation. n = 5 per time point except P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. *p < .05. (D) Quantification of NG2+; PDGFRβ− (gray), PDGFRβ+; NG2− (red) and PDGFRβ+; NG2+ (yellow) pericytes over total pericytes counted per field. n = 5 per time point except P5 (n = 3). LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm

Journal: The FASEB Journal

Article Title: Pericyte dynamics in the mouse germinal matrix angiogenesis

doi: 10.1096/fj.202200120r

Figure Lengend Snippet: FIGURE 4 Delayed NG2 expression in pericytes of the mouse GM compared to the developing cerebral CTX. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin B4 (IB4, blue) and for pericytes with anti-PDGFRβ (red) and anti-NG2.63 Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Cropped individual images (white solid boxes) of the endothelium and pericytes are displayed below each timepoint to best visualize the overlap of NG2 and PDGFRβ expression and pericyte coverage of the blood vessels (A′,B′). Note that in the CTX and the GM/SVZ, NG2 is also expressed by oligodendrocyte precursor cells beginning at E14.5; these cells were excluded from the analysis. (C) Quantification of NG2-positive pericyte coverage reveals reduced coverage at E11.5 in the GM. Scatter dot plot shows mean values with standard deviation. n = 5 per time point except P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. *p < .05. (D) Quantification of NG2+; PDGFRβ− (gray), PDGFRβ+; NG2− (red) and PDGFRβ+; NG2+ (yellow) pericytes over total pericytes counted per field. n = 5 per time point except P5 (n = 3). LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm

Article Snippet: Samples were then immunostained in PBLEC (5% Triton X- 100, 1 M MgCl2, 1 M CaCl2, and 1 M MnCl2 in 1X PBS) overnight at 4°C with Biotinylated IB4 (1:50; Vector Laboratories; Cat# BAF1042) and/or the following antibodies: goat anti- PDGFRβ (1:100; R&D Systems; Cat# BAF1042), rabbit anti- NG2 (1:700; Millipore; Cat# AB5320), rabbit anti- Desmin (1:500; Abcam; Cat# AB15200), anti– αSMA- FITC (1:200; Millipore Sigma, Cat# F3777).

Techniques: Expressing, Staining, Standard Deviation, Comparison

FIGURE 5 Desmin-positive pericyte coverage is deficient in the mouse GM. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin B4 (IB4, blue) and for pericytes with anti-PDGFRβ (red) and anti-Desmin (green).63 Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Cropped individual images (white solid boxes) of the endothelium and pericytes are displayed below each timepoint to better visualize the overlap of Desmin and PDGFRβ expression (A′,B′). Additional cropped images (dashed white boxes) are displayed in B″ to visualize reduced Desmin-positive pericyte coverage of the GM blood vessels. (C) Quantification of Desmin-positive pericyte coverage reveals significantly reduced coverage at E16.5 and E18.5 in the GM and at P5 in the SVZ. Scatter dot plot shows mean values with standard deviation. n = 5 per time point except P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. **p < .01, ***p < .001. (D) Quantification of Desmin+; PDGFRβ− (gray), PDGFRβ+; Desmin− (red) and PDGFRβ+; Desmin+ (yellow) pericytes over total pericytes counted per field. n = 5 per time point except P5 (n = 3). LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm

Journal: The FASEB Journal

Article Title: Pericyte dynamics in the mouse germinal matrix angiogenesis

doi: 10.1096/fj.202200120r

Figure Lengend Snippet: FIGURE 5 Desmin-positive pericyte coverage is deficient in the mouse GM. (A,B) High magnification images of the developing cortex (CTX) and the germinal matrix/postnatal subventricular zone (GM/SVZ) stained for blood vessels using Isolectin B4 (IB4, blue) and for pericytes with anti-PDGFRβ (red) and anti-Desmin (green).63 Purple dashed lines mark the CTX, and green dashed lines highlight the GM/SVZ regions. Cropped individual images (white solid boxes) of the endothelium and pericytes are displayed below each timepoint to better visualize the overlap of Desmin and PDGFRβ expression (A′,B′). Additional cropped images (dashed white boxes) are displayed in B″ to visualize reduced Desmin-positive pericyte coverage of the GM blood vessels. (C) Quantification of Desmin-positive pericyte coverage reveals significantly reduced coverage at E16.5 and E18.5 in the GM and at P5 in the SVZ. Scatter dot plot shows mean values with standard deviation. n = 5 per time point except P5 (n = 3). Data was analyzed using a two-way anova with Bonferroni's multiple comparison test. **p < .01, ***p < .001. (D) Quantification of Desmin+; PDGFRβ− (gray), PDGFRβ+; Desmin− (red) and PDGFRβ+; Desmin+ (yellow) pericytes over total pericytes counted per field. n = 5 per time point except P5 (n = 3). LV, lateral ventricles; E, embryonic; P, postnatal. Scale bar, 50 µm

Article Snippet: Samples were then immunostained in PBLEC (5% Triton X- 100, 1 M MgCl2, 1 M CaCl2, and 1 M MnCl2 in 1X PBS) overnight at 4°C with Biotinylated IB4 (1:50; Vector Laboratories; Cat# BAF1042) and/or the following antibodies: goat anti- PDGFRβ (1:100; R&D Systems; Cat# BAF1042), rabbit anti- NG2 (1:700; Millipore; Cat# AB5320), rabbit anti- Desmin (1:500; Abcam; Cat# AB15200), anti– αSMA- FITC (1:200; Millipore Sigma, Cat# F3777).

Techniques: Staining, Expressing, Standard Deviation, Comparison