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Creative BioMart stc2 mouse
Figure 1. Recombinant HRG binds <t>STC2</t> and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
Stc2 Mouse, supplied by Creative BioMart, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/stc2 mouse/product/Creative BioMart
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Images

1) Product Images from "Quartz Crystal Microbalance Measurement of Histidine-Rich Glycoprotein and Stanniocalcin-2 Binding to Each Other and to Inflammatory Cells."

Article Title: Quartz Crystal Microbalance Measurement of Histidine-Rich Glycoprotein and Stanniocalcin-2 Binding to Each Other and to Inflammatory Cells.

Journal: Cells

doi: 10.3390/cells11172684

Figure 1. Recombinant HRG binds STC2 and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
Figure Legend Snippet: Figure 1. Recombinant HRG binds STC2 and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.

Techniques Used: Recombinant, Immunoprecipitation, SDS Page, Control, Western Blot, Microscopy, Phagocytosis Assay



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Figure 1. Recombinant HRG binds <t>STC2</t> and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
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Figure 1. Recombinant HRG binds <t>STC2</t> and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
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Figure 1. Recombinant HRG binds <t>STC2</t> and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
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Figure 1. Recombinant HRG binds <t>STC2</t> and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
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Figure 1. Recombinant HRG binds <t>STC2</t> and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.
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Image Search Results


Microscopic image samples from staining intensity of STC2. (A) Absence of staining (DAB, ×200). (B) Weak staining (DAB, ×100). (C) Moderate staining (DAB, ×200). (D) Strong positive staining (DAB, ×100), DAB (diaminobenzidine).

Journal: Medicine

Article Title: Stanniocalcin-2 expression in glioblastoma – A novel prognostic biomarker: An observational study

doi: 10.1097/MD.0000000000038913

Figure Lengend Snippet: Microscopic image samples from staining intensity of STC2. (A) Absence of staining (DAB, ×200). (B) Weak staining (DAB, ×100). (C) Moderate staining (DAB, ×200). (D) Strong positive staining (DAB, ×100), DAB (diaminobenzidine).

Article Snippet: Subsequently, the slides were incubated with monoclonal mouse anti-rabbit STC2 antibody at a dilution ratio of 1:50 overnight at 4 °C in a humidified chamber (Abcam, Cambridge, UK).

Techniques: Staining

Relationship between  STC2  expression and clinicopathological characteristics.

Journal: Medicine

Article Title: Stanniocalcin-2 expression in glioblastoma – A novel prognostic biomarker: An observational study

doi: 10.1097/MD.0000000000038913

Figure Lengend Snippet: Relationship between STC2 expression and clinicopathological characteristics.

Article Snippet: Subsequently, the slides were incubated with monoclonal mouse anti-rabbit STC2 antibody at a dilution ratio of 1:50 overnight at 4 °C in a humidified chamber (Abcam, Cambridge, UK).

Techniques: Expressing, Adjuvant, Mutagenesis

Kaplan–Meier survival curve illustrating overall survival stratified by STC2 expression.

Journal: Medicine

Article Title: Stanniocalcin-2 expression in glioblastoma – A novel prognostic biomarker: An observational study

doi: 10.1097/MD.0000000000038913

Figure Lengend Snippet: Kaplan–Meier survival curve illustrating overall survival stratified by STC2 expression.

Article Snippet: Subsequently, the slides were incubated with monoclonal mouse anti-rabbit STC2 antibody at a dilution ratio of 1:50 overnight at 4 °C in a humidified chamber (Abcam, Cambridge, UK).

Techniques: Expressing

Kaplan–Meier survival curve illustrating progression-free survival stratified by STC2 expression.

Journal: Medicine

Article Title: Stanniocalcin-2 expression in glioblastoma – A novel prognostic biomarker: An observational study

doi: 10.1097/MD.0000000000038913

Figure Lengend Snippet: Kaplan–Meier survival curve illustrating progression-free survival stratified by STC2 expression.

Article Snippet: Subsequently, the slides were incubated with monoclonal mouse anti-rabbit STC2 antibody at a dilution ratio of 1:50 overnight at 4 °C in a humidified chamber (Abcam, Cambridge, UK).

Techniques: Expressing

Univariate and multivariate analysis of baseline characteristics for overall survival.

Journal: Medicine

Article Title: Stanniocalcin-2 expression in glioblastoma – A novel prognostic biomarker: An observational study

doi: 10.1097/MD.0000000000038913

Figure Lengend Snippet: Univariate and multivariate analysis of baseline characteristics for overall survival.

Article Snippet: Subsequently, the slides were incubated with monoclonal mouse anti-rabbit STC2 antibody at a dilution ratio of 1:50 overnight at 4 °C in a humidified chamber (Abcam, Cambridge, UK).

Techniques: Adjuvant, Mutagenesis, Expressing

Univariate and multivariate analysis of baseline characteristics for progression-free survival.

Journal: Medicine

Article Title: Stanniocalcin-2 expression in glioblastoma – A novel prognostic biomarker: An observational study

doi: 10.1097/MD.0000000000038913

Figure Lengend Snippet: Univariate and multivariate analysis of baseline characteristics for progression-free survival.

Article Snippet: Subsequently, the slides were incubated with monoclonal mouse anti-rabbit STC2 antibody at a dilution ratio of 1:50 overnight at 4 °C in a humidified chamber (Abcam, Cambridge, UK).

Techniques: Adjuvant, Mutagenesis, Expressing

Figure 1. Recombinant HRG binds STC2 and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.

Journal: Cells

Article Title: Quartz Crystal Microbalance Measurement of Histidine-Rich Glycoprotein and Stanniocalcin-2 Binding to Each Other and to Inflammatory Cells.

doi: 10.3390/cells11172684

Figure Lengend Snippet: Figure 1. Recombinant HRG binds STC2 and modulates phagocytosis of bioparticles. (A) Co- immunoprecipitation of HRG but not inactive HRG with STC2. Recombinant proteins (2 µg each) were separated on SDS-PAGE as individual preparations (loading control) or after mixing and im- munoprecipitation (IP) using antibodies against STC2, followed by immunoblotting (IB) as indicated. (B) Ratio of HRG (active or inactive) band intensities in the STC2 immunoprecipitate normalized to corresponding active and inactive HRG loading controls. Statistical analysis; Student’s t-test. (C) Representative microscope images of U937 monocytes without (left) or with treatment with active HRG (right) in the phagocytosis assay. Green cells have engulfed pH-sensitive fluorescent bioparticles. Scale bar; 50 µm. (D) Quantification of phagocytosis efficiency in the different treatment conditions. The proportion of positive (green) phagocytotic U937 cells to all cells per field of vision is shown in relation to the positive cells/total cells in the vitD3 differentiated HRG-treated condition (set to 1). Statistical analysis; Tukey’s multiple comparisons test (D). *** p < 0.001; **** p < 0.0001.

Article Snippet: At the start of the experiment, cells were incubated with 10 nM vitD3, recombinant, in-house purified HRG (mouse) at 1 μg/mL (13.3 nM) [24], and STC2 (mouse) (cat. no. STC2-16118 M, Creative Biomart, Shirley, NY, USA) or inactive HRG protein at equivalent molar concentrations together with sterile green E. coli bioparticles (cat. no. 4616, Essen Bioscience, Ann Arbor, MI, USA) at 33 μg/mL.

Techniques: Recombinant, Immunoprecipitation, SDS Page, Control, Western Blot, Microscopy, Phagocytosis Assay