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Proteintech anti ccnd1 mouse monoclonal antibody
CXCL12 overexpression and knockdown in GCs. (A,B) Changes in the expression of CXCL12 after its overexpression and knockdown in GCs. (C,D) The mRNA expression level of PCNA , <t>CCND1</t> , CDK2 , Bcl-2 and Bax was detected after overexpressing or knocking down CXCL12 in GCs. (E) The protein expression levels of CCND1, PCNA, Bcl-2 and Bax were detected after overexpressing and knocking down CXCL12 in GCs. H, high-litter size group; L, low-itter size group; GAPDH was selected as the internal reference gene (The t test was used for the above analyses comparing two individual samples. * p<0.05; ** p<0.01; *** p<0.001; ns, not significant). GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GC, granulosa cells.
Anti Ccnd1 Mouse Monoclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CXCL12 overexpression and knockdown in GCs. (A,B) Changes in the expression of CXCL12 after its overexpression and knockdown in GCs. (C,D) The mRNA expression level of PCNA , <t>CCND1</t> , CDK2 , Bcl-2 and Bax was detected after overexpressing or knocking down CXCL12 in GCs. (E) The protein expression levels of CCND1, PCNA, Bcl-2 and Bax were detected after overexpressing and knocking down CXCL12 in GCs. H, high-litter size group; L, low-itter size group; GAPDH was selected as the internal reference gene (The t test was used for the above analyses comparing two individual samples. * p<0.05; ** p<0.01; *** p<0.001; ns, not significant). GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GC, granulosa cells.
Anti Ccnd1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Proteintech antibodies against cyclin d1 ccnd1
Different doses of RRP promote liver regeneration at 48 h post-PHx in mice. ( A ) Experimental design of PHx surgery, RRP administration (L, M, and H correspond to 2.5, 5, or 10 g/kg, respectively), and sample collection at 48 h post-PHx. ( B ) Liver coefficient. ( C ) Serum levels of ALT and AST. ( D ) H & E staining and immunohistochemistry of Ki67 and <t>CCND1</t> in liver sections at 48 h post-PHx in the control and RRP-treated groups (2.5, 5, and 10 g/kg). Scale bar = 100 μm. ( E ) AOD quantification of KI67 and CCND1. ( F ) Relative mRNA expression of Ccnd1 and Ki67 in liver from each group was determined by qPCR and normalized using Hprt1 as an internal control. Statistical significance: ** p < 0.01, *** p < 0.001, **** p < 0.0001 as compared with the control group; # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 as compared with the PHx group ( n = 6 for mice).
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Proteintech rabbit anti ccnd1
Different doses of RRP promote liver regeneration at 48 h post-PHx in mice. ( A ) Experimental design of PHx surgery, RRP administration (L, M, and H correspond to 2.5, 5, or 10 g/kg, respectively), and sample collection at 48 h post-PHx. ( B ) Liver coefficient. ( C ) Serum levels of ALT and AST. ( D ) H & E staining and immunohistochemistry of Ki67 and <t>CCND1</t> in liver sections at 48 h post-PHx in the control and RRP-treated groups (2.5, 5, and 10 g/kg). Scale bar = 100 μm. ( E ) AOD quantification of KI67 and CCND1. ( F ) Relative mRNA expression of Ccnd1 and Ki67 in liver from each group was determined by qPCR and normalized using Hprt1 as an internal control. Statistical significance: ** p < 0.01, *** p < 0.001, **** p < 0.0001 as compared with the control group; # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 as compared with the PHx group ( n = 6 for mice).
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Average 96 stars, based on 1 article reviews
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CXCL12 overexpression and knockdown in GCs. (A,B) Changes in the expression of CXCL12 after its overexpression and knockdown in GCs. (C,D) The mRNA expression level of PCNA , CCND1 , CDK2 , Bcl-2 and Bax was detected after overexpressing or knocking down CXCL12 in GCs. (E) The protein expression levels of CCND1, PCNA, Bcl-2 and Bax were detected after overexpressing and knocking down CXCL12 in GCs. H, high-litter size group; L, low-itter size group; GAPDH was selected as the internal reference gene (The t test was used for the above analyses comparing two individual samples. * p<0.05; ** p<0.01; *** p<0.001; ns, not significant). GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GC, granulosa cells.

Journal: Animal Bioscience

Article Title: Transcriptomic analysis identifies CXCL12 as a novel candidate gene for litter size in rabbits

doi: 10.5713/ab.24.0640

Figure Lengend Snippet: CXCL12 overexpression and knockdown in GCs. (A,B) Changes in the expression of CXCL12 after its overexpression and knockdown in GCs. (C,D) The mRNA expression level of PCNA , CCND1 , CDK2 , Bcl-2 and Bax was detected after overexpressing or knocking down CXCL12 in GCs. (E) The protein expression levels of CCND1, PCNA, Bcl-2 and Bax were detected after overexpressing and knocking down CXCL12 in GCs. H, high-litter size group; L, low-itter size group; GAPDH was selected as the internal reference gene (The t test was used for the above analyses comparing two individual samples. * p<0.05; ** p<0.01; *** p<0.001; ns, not significant). GAPDH, glyceraldehyde-3-phosphate dehydrogenase; GC, granulosa cells.

Article Snippet: Protein detection was achieved using the following antibodies: anti-CCND1 mouse monoclonal antibody (1:250, Proteintech), anti-PCNA rabbit polyclonal antibody (1:250, Proteintech), anti-Bcl2 rabbit polyclonal antibody (1:250, Proteintech), anti-Bax rabbit polyclonal antibody (1:250, Proteintech), anti-CITED1 rabbit polyclonal antibody (1:50, Proteintech), anti-WNT10B mouse monoclonal polyclonal antibody (1:250, Proteintech), anti-CXCR4 mouse monoclonal polyclonal antibody (1:250, Proteintech), anti-phospho-JAK2 rabbit monoclonal polyclonal antibody (1:250, Abcam, Cambridge, UK), anti-JAK2 rabbit monoclonal polyclonal antibody (1:250, Abcam), anti-phospho-STAT1 rabbit polyclonal antibody (1:250, Proteintech), anti-STAT1 rabbit polyclonal antibody (1:250, Proteintech), anti-GAPDH mouse monoclonal antibody (1:2,500, Proteintech), 1:1,000 goat anti-rabbit secondary antibody IgG (Proteintech) and 1:1,000 goat anti-mouse secondary antibody IgG (Proteintech).

Techniques: Over Expression, Knockdown, Expressing

Different doses of RRP promote liver regeneration at 48 h post-PHx in mice. ( A ) Experimental design of PHx surgery, RRP administration (L, M, and H correspond to 2.5, 5, or 10 g/kg, respectively), and sample collection at 48 h post-PHx. ( B ) Liver coefficient. ( C ) Serum levels of ALT and AST. ( D ) H & E staining and immunohistochemistry of Ki67 and CCND1 in liver sections at 48 h post-PHx in the control and RRP-treated groups (2.5, 5, and 10 g/kg). Scale bar = 100 μm. ( E ) AOD quantification of KI67 and CCND1. ( F ) Relative mRNA expression of Ccnd1 and Ki67 in liver from each group was determined by qPCR and normalized using Hprt1 as an internal control. Statistical significance: ** p < 0.01, *** p < 0.001, **** p < 0.0001 as compared with the control group; # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 as compared with the PHx group ( n = 6 for mice).

Journal: Nutrients

Article Title: Radix Rehmanniae Praeparata Extract Enhances Liver Regeneration Through AMPK-Driven Metabolic Reprogramming

doi: 10.3390/nu17223579

Figure Lengend Snippet: Different doses of RRP promote liver regeneration at 48 h post-PHx in mice. ( A ) Experimental design of PHx surgery, RRP administration (L, M, and H correspond to 2.5, 5, or 10 g/kg, respectively), and sample collection at 48 h post-PHx. ( B ) Liver coefficient. ( C ) Serum levels of ALT and AST. ( D ) H & E staining and immunohistochemistry of Ki67 and CCND1 in liver sections at 48 h post-PHx in the control and RRP-treated groups (2.5, 5, and 10 g/kg). Scale bar = 100 μm. ( E ) AOD quantification of KI67 and CCND1. ( F ) Relative mRNA expression of Ccnd1 and Ki67 in liver from each group was determined by qPCR and normalized using Hprt1 as an internal control. Statistical significance: ** p < 0.01, *** p < 0.001, **** p < 0.0001 as compared with the control group; # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 as compared with the PHx group ( n = 6 for mice).

Article Snippet: Paraffin sections underwent antigen retrieval; endogenous peroxidase blocking with 3% H 2 O 2 ; and overnight incubation with primary antibodies against Cyclin D1 (Ccnd1) (Proteintech, 1:100), Marker of proliferation Ki-67 (Ki67) (Proteintech, 1:600), and H3K27ac (CST, 1:100) in a wet chamber at 4 °C.

Techniques: Staining, Immunohistochemistry, Control, Expressing

RRP promotes early and sustained hepatocyte proliferation and alleviates liver injury after PHx. ( A ) Experimental timeline of 70% PHx and RRP treatment (5 g/kg). ( B ) Liver coefficient. ( C ) Serum levels of ALT and AST. ( D ) H & E, KI67, and CCND1 staining of liver sections at 24 h and 96 h post-PHx with or without RRP treatment. Scale bar = 100 μm. ( E ) AOD quantification of KI67 and CCND1. ( F ) Relative mRNA expression of Ccnd1 and Ki67 in liver, normalized to Hprt1. Statistical significance: ** p < 0.01, **** p < 0.0001 as compared with the control group; # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 as compared with the PHx group without RRP treatment; $$$$ p < 0.0001 between indicated groups ( n = 6 for mice).

Journal: Nutrients

Article Title: Radix Rehmanniae Praeparata Extract Enhances Liver Regeneration Through AMPK-Driven Metabolic Reprogramming

doi: 10.3390/nu17223579

Figure Lengend Snippet: RRP promotes early and sustained hepatocyte proliferation and alleviates liver injury after PHx. ( A ) Experimental timeline of 70% PHx and RRP treatment (5 g/kg). ( B ) Liver coefficient. ( C ) Serum levels of ALT and AST. ( D ) H & E, KI67, and CCND1 staining of liver sections at 24 h and 96 h post-PHx with or without RRP treatment. Scale bar = 100 μm. ( E ) AOD quantification of KI67 and CCND1. ( F ) Relative mRNA expression of Ccnd1 and Ki67 in liver, normalized to Hprt1. Statistical significance: ** p < 0.01, **** p < 0.0001 as compared with the control group; # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 as compared with the PHx group without RRP treatment; $$$$ p < 0.0001 between indicated groups ( n = 6 for mice).

Article Snippet: Paraffin sections underwent antigen retrieval; endogenous peroxidase blocking with 3% H 2 O 2 ; and overnight incubation with primary antibodies against Cyclin D1 (Ccnd1) (Proteintech, 1:100), Marker of proliferation Ki-67 (Ki67) (Proteintech, 1:600), and H3K27ac (CST, 1:100) in a wet chamber at 4 °C.

Techniques: Staining, Expressing, Control

AMPK inhibition impairs RRP-induced metabolic remodeling and hepatocyte proliferation post-PHx. ( A ) Experimental timeline showing PHx, RRP administration (5 mg/kg), and Compound C (20 mg/kg) intervention. ( B ) Western blot analysis of pACC, ACC, pAMPK, and AMPK protein levels. ( C ) Hepatic acetyl-CoA levels. ( D ) Relative mRNA expression of Ccnd1 and Ki67 in liver from each group was determined by qPCR and normalized using Hprt1 as an internal control. ( E ) H&E and immunohistochemical staining for KI67, CCND1, and H3K27ac, with AOD quantitative analysis. ( F , G ) Serum levels of ALT and AST. Scale bar = 100 μm. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 as compared with the PHx group; # p < 0.05, ### p < 0.001, #### p < 0.0001 as compared with the PHx + RRP group ( n = 6 for mice).

Journal: Nutrients

Article Title: Radix Rehmanniae Praeparata Extract Enhances Liver Regeneration Through AMPK-Driven Metabolic Reprogramming

doi: 10.3390/nu17223579

Figure Lengend Snippet: AMPK inhibition impairs RRP-induced metabolic remodeling and hepatocyte proliferation post-PHx. ( A ) Experimental timeline showing PHx, RRP administration (5 mg/kg), and Compound C (20 mg/kg) intervention. ( B ) Western blot analysis of pACC, ACC, pAMPK, and AMPK protein levels. ( C ) Hepatic acetyl-CoA levels. ( D ) Relative mRNA expression of Ccnd1 and Ki67 in liver from each group was determined by qPCR and normalized using Hprt1 as an internal control. ( E ) H&E and immunohistochemical staining for KI67, CCND1, and H3K27ac, with AOD quantitative analysis. ( F , G ) Serum levels of ALT and AST. Scale bar = 100 μm. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 as compared with the PHx group; # p < 0.05, ### p < 0.001, #### p < 0.0001 as compared with the PHx + RRP group ( n = 6 for mice).

Article Snippet: Paraffin sections underwent antigen retrieval; endogenous peroxidase blocking with 3% H 2 O 2 ; and overnight incubation with primary antibodies against Cyclin D1 (Ccnd1) (Proteintech, 1:100), Marker of proliferation Ki-67 (Ki67) (Proteintech, 1:600), and H3K27ac (CST, 1:100) in a wet chamber at 4 °C.

Techniques: Inhibition, Western Blot, Expressing, Control, Immunohistochemical staining, Staining