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arg2 polyclonal antibody (Proteintech)

Name: arg2 polyclonal antibody
Brand: Proteintech
Rating: 93 (18 reviews)

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Proteintech arg2 polyclonal antibody
Arg2 Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/arg2 polyclonal antibody/product/Proteintech
Average 93 stars, based on 18 article reviews

arg2 polyclonal antibody - by Bioz Stars, 2026-02

93/100 stars

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ARG2 is upregulated in the CI-AKI mice kidneys and primary tubular epithelial cells, and increased in blood samples of CI-AKI mice and patients. (A) Heat map of proteomics in iohexol-induced AKI mice. P-Value <0.05 and log2 fold change (FC) > 2. (B) Heat map of transcriptomics in iohexol-induced AKI mice. P-Value <0.0001 and log2 fold change (FC) > 3. (C–E) The ARG2 protein and mRNA expressions were evaluated in the kidneys of mice treated with iohexol. (F) Representative images of immunohistochemistry staining of ARG2 in the kidneys of iohexol-induced AKI mice. The red arrows indicate deeper ARG2-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (G) Representative images of the immunofluorescence colocalization of CD31, F4/80, LTL, PNA, and DBA with ARG2 in the kidney of iohexol-induced AKI mice. The following specific markers were used: endothelial, CD31; macrophage, F4/80; proximal tubule, lotus tetragonolobus lectin (LTL); distal tubule, peanut agglutinin (PNA); and collecting duct, dolichos biflorus agglutinin (DBA). The white arrows indicate positive tubules with colocalization of ARG2 and specific tubular markers. Scale, 50 μm. (H–J) ARG2 protein and mRNA expressions in primary tubular epithelial cells treated with iohexol. (K) Representative image of ARG2 and mito-tracker immunofluorescence colocalization in HK-2 cells. The orange arrows indicate that iohexol causes a decrease in mitochondrial fluorescence. The white arrows indicate the normal colocalization of ARG2 with mitochondria. The yellow arrows indicate that iohexol leads to reduced colocalization of ARG2 with mitochondria. Scale, 20 μm. (L and M) Serum levels of ARG2 in CI-AKI mice (L) and patients (M). * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 5-6 in mice, n = 3–6 in HK-2 cells.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 is upregulated in the CI-AKI mice kidneys and primary tubular epithelial cells, and increased in blood samples of CI-AKI mice and patients. (A) Heat map of proteomics in iohexol-induced AKI mice. P-Value <0.05 and log2 fold change (FC) > 2. (B) Heat map of transcriptomics in iohexol-induced AKI mice. P-Value <0.0001 and log2 fold change (FC) > 3. (C–E) The ARG2 protein and mRNA expressions were evaluated in the kidneys of mice treated with iohexol. (F) Representative images of immunohistochemistry staining of ARG2 in the kidneys of iohexol-induced AKI mice. The red arrows indicate deeper ARG2-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (G) Representative images of the immunofluorescence colocalization of CD31, F4/80, LTL, PNA, and DBA with ARG2 in the kidney of iohexol-induced AKI mice. The following specific markers were used: endothelial, CD31; macrophage, F4/80; proximal tubule, lotus tetragonolobus lectin (LTL); distal tubule, peanut agglutinin (PNA); and collecting duct, dolichos biflorus agglutinin (DBA). The white arrows indicate positive tubules with colocalization of ARG2 and specific tubular markers. Scale, 50 μm. (H–J) ARG2 protein and mRNA expressions in primary tubular epithelial cells treated with iohexol. (K) Representative image of ARG2 and mito-tracker immunofluorescence colocalization in HK-2 cells. The orange arrows indicate that iohexol causes a decrease in mitochondrial fluorescence. The white arrows indicate the normal colocalization of ARG2 with mitochondria. The yellow arrows indicate that iohexol leads to reduced colocalization of ARG2 with mitochondria. Scale, 20 μm. (L and M) Serum levels of ARG2 in CI-AKI mice (L) and patients (M). * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 5-6 in mice, n = 3–6 in HK-2 cells.

Article Snippet: The following uses are made using antibodies and fluorescent dyes: anti-ARG2 (Bioss, bs-11397R), CD31 (Wuhan Servicebio Technology, GB11063-2), F4/80 (Wuhan Servicebio Technology, Q61549), Lotus Tetragonolobus Lectin (LTL) Fluorescein (Vector, FL-1321), Peanut Agglutinin (PNA) Fluorescein (Vector, FL-1071), Dolichos Biflorus Agglutinin (DBA) Fluorescein (Vector, FL-1031), DAPI (Wuhan Servicebio Technology, G1012).

Techniques: Immunohistochemistry, Staining, Immunofluorescence, Fluorescence

ARG2 inhibition and deficiency significantly ameliorate iohexol-induced AKI. (A–D) Renal function and renal tissue injury of iohexol-induced AKI mice treated with nor-NOHA were assessed by SCr, BUN, and tubular injury score. Scale, 20×, 100 μm, 40×, 50 μm. (E–H) Renal function and renal tissue injury of ARG2 KO and WT mice injected by iohexol via tail vein were assessed by SCr, BUN, and tubular injury score. The red arrows indicate the vacuolar degeneration of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 inhibition and deficiency significantly ameliorate iohexol-induced AKI. (A–D) Renal function and renal tissue injury of iohexol-induced AKI mice treated with nor-NOHA were assessed by SCr, BUN, and tubular injury score. Scale, 20×, 100 μm, 40×, 50 μm. (E–H) Renal function and renal tissue injury of ARG2 KO and WT mice injected by iohexol via tail vein were assessed by SCr, BUN, and tubular injury score. The red arrows indicate the vacuolar degeneration of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6.

Techniques: Inhibition, Injection

ARG2 deficiency significantly reduces apoptosis in iohexol-induced AKI mice and HK-2 cells. (A and B) Representative images of TUNEL staining in ARG2 KO and WT mice treated with iohexol. TUNEL-positive cells and nuclei were indicated by green and blue fluorescence, respectively. (C–F) The protein expressions of caspase-3, cleaved caspase-3, Bcl-2, and Bax were evaluated with western blotting in ARG2 KO and WT mice administrated with iohexol. β-actin was used as the loading control. (G–K) Western blotting was used to evaluate the protein expressions of ARG2, caspase-3, cleaved caspase-3, Bcl-2, and Bax in HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. (L and M) TUNEL staining was performed to examine apoptotic HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. TUNEL-positive cells and nuclei were indicated by green and blue fluorescence, respectively. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-6 in HK-2 cells.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 deficiency significantly reduces apoptosis in iohexol-induced AKI mice and HK-2 cells. (A and B) Representative images of TUNEL staining in ARG2 KO and WT mice treated with iohexol. TUNEL-positive cells and nuclei were indicated by green and blue fluorescence, respectively. (C–F) The protein expressions of caspase-3, cleaved caspase-3, Bcl-2, and Bax were evaluated with western blotting in ARG2 KO and WT mice administrated with iohexol. β-actin was used as the loading control. (G–K) Western blotting was used to evaluate the protein expressions of ARG2, caspase-3, cleaved caspase-3, Bcl-2, and Bax in HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. (L and M) TUNEL staining was performed to examine apoptotic HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. TUNEL-positive cells and nuclei were indicated by green and blue fluorescence, respectively. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-6 in HK-2 cells.

Techniques: TUNEL Assay, Staining, Fluorescence, Western Blot, Control, Transfection, Incubation

ARG2 mediates nitrosative stress in iohexol-induced AKI and HK-2 cells. (A and B) The protein expression of 3-NT was evaluated by western blotting in ARG2 KO and WT mice treated with iohexol. (C and D) Representative images of immunohistochemistry staining of 3-NT in the kidneys of ARG2 KO and WT mice treated with iohexol. The red arrows indicate deeper 3-NT-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (E and F) The expression of 3-NT was evaluated with western blotting in HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. (G and H) The level of ONOO − was evaluated with immunofluorescence in HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. Green fluorescence indicates ONOO − . The number of cells was counted by DPC. DPC, Digital phase contrast. Scale, 100 μm * P < 0.05, ** P < 0.01, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-10 in HK-2 cells.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 mediates nitrosative stress in iohexol-induced AKI and HK-2 cells. (A and B) The protein expression of 3-NT was evaluated by western blotting in ARG2 KO and WT mice treated with iohexol. (C and D) Representative images of immunohistochemistry staining of 3-NT in the kidneys of ARG2 KO and WT mice treated with iohexol. The red arrows indicate deeper 3-NT-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (E and F) The expression of 3-NT was evaluated with western blotting in HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. (G and H) The level of ONOO − was evaluated with immunofluorescence in HK-2 cells transfected with ARG2 siRNA and incubated with iohexol. Green fluorescence indicates ONOO − . The number of cells was counted by DPC. DPC, Digital phase contrast. Scale, 100 μm * P < 0.05, ** P < 0.01, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-10 in HK-2 cells.

Techniques: Expressing, Western Blot, Immunohistochemistry, Staining, Transfection, Incubation, Immunofluorescence, Fluorescence

HO-1 is involved in ARG2 mediated nitrosative stress. (A) Correlation between ARG2 protein expression and significantly different proteins of proteomics. X-axis, R with ARG2; Y-axis, P -value. (B) The HO-1 mRNA expression was evaluated in mice treated with iohexol. (C and D) The HO-1 protein expression was evaluated by western blotting in ARG2 KO and WT mice administrated with iohexol. (E–G) The HO-1 mRNA and protein expressions were evaluated in primary tubular epithelial cells incubated with iohexol. (H and I) The level of ONOO − was evaluated by immunofluorescence in HK-2 cells transfected with HO-1 overexpression plasmid or cultured with iohexol. Green fluorescence indicates ONOO − . The number of cells was counted by DPC. DPC, Digital phase contrast. Scale, 100 μm. (J and K) The 3-NT protein expression was evaluated by western blotting in HK-2 cells incubated with iohexol and transfected with ARG2 overexpression plasmid and HO-1 overexpression plasmid. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-6 in cells.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: HO-1 is involved in ARG2 mediated nitrosative stress. (A) Correlation between ARG2 protein expression and significantly different proteins of proteomics. X-axis, R with ARG2; Y-axis, P -value. (B) The HO-1 mRNA expression was evaluated in mice treated with iohexol. (C and D) The HO-1 protein expression was evaluated by western blotting in ARG2 KO and WT mice administrated with iohexol. (E–G) The HO-1 mRNA and protein expressions were evaluated in primary tubular epithelial cells incubated with iohexol. (H and I) The level of ONOO − was evaluated by immunofluorescence in HK-2 cells transfected with HO-1 overexpression plasmid or cultured with iohexol. Green fluorescence indicates ONOO − . The number of cells was counted by DPC. DPC, Digital phase contrast. Scale, 100 μm. (J and K) The 3-NT protein expression was evaluated by western blotting in HK-2 cells incubated with iohexol and transfected with ARG2 overexpression plasmid and HO-1 overexpression plasmid. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-6 in cells.

Techniques: Expressing, Western Blot, Incubation, Immunofluorescence, Transfection, Over Expression, Plasmid Preparation, Cell Culture, Fluorescence

ARG2 inhibits the expression of HO-1 at the transcriptional level in HK-2 cell cultured with iohexol. (A–D) The HO-1 protein expression was examined by western blotting in HK-2 cells transfected with ARG2 siRNA or ARG2 overexpression plasmid, and incubated with iohexol. (E and F) The HO-1 mRNA expression was evaluated in HK-2 cells transfected with ARG2 siRNA or ARG2 overexpression, and incubated with iohexol. (G and H) The ARG2 protein expression was evaluated with western blotting in HK-2 cells transfected with HO-1 siRNA or cultured with iohexol. (I and J) The ARG2 protein expression was evaluated with western blotting in HK-2 cells cultured with CoPP and iohexol. (K and L) The HO-1 protein expression was evaluated with western blotting in HK-2 cells transfected with ARG2 siRNA or cultured with CHX. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 3-6 in HK-2 cells.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 inhibits the expression of HO-1 at the transcriptional level in HK-2 cell cultured with iohexol. (A–D) The HO-1 protein expression was examined by western blotting in HK-2 cells transfected with ARG2 siRNA or ARG2 overexpression plasmid, and incubated with iohexol. (E and F) The HO-1 mRNA expression was evaluated in HK-2 cells transfected with ARG2 siRNA or ARG2 overexpression, and incubated with iohexol. (G and H) The ARG2 protein expression was evaluated with western blotting in HK-2 cells transfected with HO-1 siRNA or cultured with iohexol. (I and J) The ARG2 protein expression was evaluated with western blotting in HK-2 cells cultured with CoPP and iohexol. (K and L) The HO-1 protein expression was evaluated with western blotting in HK-2 cells transfected with ARG2 siRNA or cultured with CHX. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 3-6 in HK-2 cells.

Techniques: Expressing, Cell Culture, Western Blot, Transfection, Over Expression, Plasmid Preparation, Incubation

CREB1 regulates ARG2 transcription. (A) Luciferase reporter gene results demonstrated that CREB1 combined with ARG2 promoter. (B) ChIP-PCR showed a direct combination and enrichment of CREB1 to the promoter region of ARG2. (C and D) The P-CREB1 and CREB1 protein expressions were evaluated in mice treated with iohexol. (E and F) The P-CREB1 and CREB1 protein expressions were evaluated in HK-2 cells cultured with iohexol at the indicated time points. (G–J) The CREB1 and ARG2 protein expression were evaluated in HK-2 cells transfected with CREB1 siRNA. (K and L) The CREB1 protein expression was evaluated in HK-2 cells transfected with ARG2 overexpression plasmid. * P < 0.05, ** P < 0.01, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-6 in HK-2 cells.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: CREB1 regulates ARG2 transcription. (A) Luciferase reporter gene results demonstrated that CREB1 combined with ARG2 promoter. (B) ChIP-PCR showed a direct combination and enrichment of CREB1 to the promoter region of ARG2. (C and D) The P-CREB1 and CREB1 protein expressions were evaluated in mice treated with iohexol. (E and F) The P-CREB1 and CREB1 protein expressions were evaluated in HK-2 cells cultured with iohexol at the indicated time points. (G–J) The CREB1 and ARG2 protein expression were evaluated in HK-2 cells transfected with CREB1 siRNA. (K and L) The CREB1 protein expression was evaluated in HK-2 cells transfected with ARG2 overexpression plasmid. * P < 0.05, ** P < 0.01, **** P < 0.0001. mean ± SD, n = 6 in mice, n = 3-6 in HK-2 cells.

Techniques: Luciferase, Cell Culture, Expressing, Transfection, Over Expression, Plasmid Preparation

ARG2 may be a potential target of cisplatin-induced AKI. (A–C) ARG2 protein and mRNA expressions in the kidneys of cisplatin-induced AKI mice. (D) Representative images of immunohistochemistry staining of ARG2 in cisplatin-induced AKI mice kidneys. The red arrows indicate deeper ARG2-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (E) Representative images of the immunofluorescence colocalization of CD31, F4/80, LTL, PNA, and DBA with ARG2 in the kidney of cisplatin-induced AKI mice. The following specific markers were used: endothelial, CD31; macrophage, F4/80; proximal tubule, lotus tetragonolobus lectin (LTL); distal tubule, peanut agglutinin (PNA); and collecting duct, dolichos biflorus agglutinin (DBA). The white arrows indicate positive tubules with colocalization of ARG2 and specific tubular markers. Scale, 50 μm. (F and G) ARG2 protein expression in primary tubular epithelial cells treated by cisplatin. (H–K) Renal function and renal tissue injury of ARG2 KO and WT mice administrated with cisplatin were assessed by SCr, BUN, and tubular injury score. The red arrows showed the vacuolar degeneration, tubular necrosis, cast formation, and tubular dilation of renal tubules. (L and M) The HO-1 protein expression was evaluated by western blotting in ARG2 KO and WT mice administrated with cisplatin. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 may be a potential target of cisplatin-induced AKI. (A–C) ARG2 protein and mRNA expressions in the kidneys of cisplatin-induced AKI mice. (D) Representative images of immunohistochemistry staining of ARG2 in cisplatin-induced AKI mice kidneys. The red arrows indicate deeper ARG2-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (E) Representative images of the immunofluorescence colocalization of CD31, F4/80, LTL, PNA, and DBA with ARG2 in the kidney of cisplatin-induced AKI mice. The following specific markers were used: endothelial, CD31; macrophage, F4/80; proximal tubule, lotus tetragonolobus lectin (LTL); distal tubule, peanut agglutinin (PNA); and collecting duct, dolichos biflorus agglutinin (DBA). The white arrows indicate positive tubules with colocalization of ARG2 and specific tubular markers. Scale, 50 μm. (F and G) ARG2 protein expression in primary tubular epithelial cells treated by cisplatin. (H–K) Renal function and renal tissue injury of ARG2 KO and WT mice administrated with cisplatin were assessed by SCr, BUN, and tubular injury score. The red arrows showed the vacuolar degeneration, tubular necrosis, cast formation, and tubular dilation of renal tubules. (L and M) The HO-1 protein expression was evaluated by western blotting in ARG2 KO and WT mice administrated with cisplatin. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6.

Techniques: Immunohistochemistry, Staining, Immunofluorescence, Expressing, Western Blot

ARG2 may be a potential target of vancomycin-induced AKI. (A–C) ARG2 protein and mRNA expressions in the kidneys of vancomycin-induced AKI mice. (D) Representative images of immunohistochemistry staining of ARG2 in vancomycin-induced AKI mice kidneys. The red arrows indicate deeper ARG2-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (E) Representative images of the immunofluorescence colocalization of CD31, F4/80, LTL, PNA, and DBA with ARG2 in the kidney of vancomycin-induced AKI mice. The following specific markers were used: endothelial, CD31; macrophage, F4/80; proximal tubule, lotus tetragonolobus lectin (LTL); distal tubule, peanut agglutinin (PNA); and collecting duct, dolichos biflorus agglutinin (DBA). The white arrows indicate positive tubules with colocalization of ARG2 and specific tubular markers. Scale, 50 μm. (F and G) ARG2 protein expression in primary tubular epithelial cells treated by vancomycin. (H–K) Renal function and renal tissue injury of ARG2 KO and WT mice administrated with vancomycin were assessed by SCr, BUN, and tubular injury score. The red arrows showed the vacuolar degeneration, tubular necrosis, cast formation, and tubular dilation of renal tubules. (L and M) The HO-1 protein expression was evaluated by western blotting in ARG2 KO and WT mice administrated with vancomycin. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6.

Journal: Redox Biology

Article Title: Arginase2 mediates contrast-induced acute kidney injury via facilitating nitrosative stress in tubular cells

doi: 10.1016/j.redox.2023.102929

Figure Lengend Snippet: ARG2 may be a potential target of vancomycin-induced AKI. (A–C) ARG2 protein and mRNA expressions in the kidneys of vancomycin-induced AKI mice. (D) Representative images of immunohistochemistry staining of ARG2 in vancomycin-induced AKI mice kidneys. The red arrows indicate deeper ARG2-positive staining of renal tubules. Scale, 20×, 100 μm, 40×, 50 μm. (E) Representative images of the immunofluorescence colocalization of CD31, F4/80, LTL, PNA, and DBA with ARG2 in the kidney of vancomycin-induced AKI mice. The following specific markers were used: endothelial, CD31; macrophage, F4/80; proximal tubule, lotus tetragonolobus lectin (LTL); distal tubule, peanut agglutinin (PNA); and collecting duct, dolichos biflorus agglutinin (DBA). The white arrows indicate positive tubules with colocalization of ARG2 and specific tubular markers. Scale, 50 μm. (F and G) ARG2 protein expression in primary tubular epithelial cells treated by vancomycin. (H–K) Renal function and renal tissue injury of ARG2 KO and WT mice administrated with vancomycin were assessed by SCr, BUN, and tubular injury score. The red arrows showed the vacuolar degeneration, tubular necrosis, cast formation, and tubular dilation of renal tubules. (L and M) The HO-1 protein expression was evaluated by western blotting in ARG2 KO and WT mice administrated with vancomycin. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001. mean ± SD, n = 6.

Techniques: Immunohistochemistry, Staining, Immunofluorescence, Expressing, Western Blot

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