cell cycle control Search Results


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NuAire humidity
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Boster Bio fxr
Impacts of Limonin <t>upon</t> <t>FXR/FGF15</t> signaling pathway in intestinal of hyperlipidemia mice. ( A ) Representative picture of immunofluorescence expression in mice intestine. ( B ) The immunofluorescence protein expression of FGF15 in the ileum. ( C ) The immunofluorescence protein expression of FXR in the ileum. ( D ) Ileum mRNA expression levels of Fgf15 . ( E ) Ileum mRNA expression levels of Fxr . ( F ) Ileum mRNA expression levels of Asbt . ( G ) Representative protein bands detected by WB. ( H ) Ileum protein expression levels of FGF15. ( I ) Ileum protein expression levels of FXR. ( J ) Ileum protein expression levels of ASBT. Values are shown as mean ± SD ( n = 3). # P < 0.05, ## P < 0.01 vs. MG and * P < 0.05, ** P < 0.01 vs. NG
Fxr, supplied by Boster Bio, 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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NuAire культивирование клеток выполняли в ин кубаторе nu 5840e
Impacts of Limonin <t>upon</t> <t>FXR/FGF15</t> signaling pathway in intestinal of hyperlipidemia mice. ( A ) Representative picture of immunofluorescence expression in mice intestine. ( B ) The immunofluorescence protein expression of FGF15 in the ileum. ( C ) The immunofluorescence protein expression of FXR in the ileum. ( D ) Ileum mRNA expression levels of Fgf15 . ( E ) Ileum mRNA expression levels of Fxr . ( F ) Ileum mRNA expression levels of Asbt . ( G ) Representative protein bands detected by WB. ( H ) Ileum protein expression levels of FGF15. ( I ) Ileum protein expression levels of FXR. ( J ) Ileum protein expression levels of ASBT. Values are shown as mean ± SD ( n = 3). # P < 0.05, ## P < 0.01 vs. MG and * P < 0.05, ** P < 0.01 vs. NG
культивирование клеток выполняли в ин кубаторе Nu 5840e, supplied by NuAire, 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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Boster Bio p cdc2 boster
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
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Boster Bio cdk13
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
Cdk13, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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New Science Press Ltd the cell cycle: principles of control
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
The Cell Cycle: Principles Of Control, supplied by New Science Press Ltd, 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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Johns Hopkins HealthCare proteins that control cell cycle progression also drive multiciliated cell differentiation
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
Proteins That Control Cell Cycle Progression Also Drive Multiciliated Cell Differentiation, supplied by Johns Hopkins HealthCare, 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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Viollier AG cell cycle control by the master regulator ctra in sinorhizobium meliloti
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
Cell Cycle Control By The Master Regulator Ctra In Sinorhizobium Meliloti, supplied by Viollier AG, 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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Viollier AG functional dichotomy and distinct nanoscale assemblies of a cell cycle-controlled bipolar zincfinger regulator
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
Functional Dichotomy And Distinct Nanoscale Assemblies Of A Cell Cycle Controlled Bipolar Zincfinger Regulator, supplied by Viollier AG, 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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Proteos Inc cell cycle control and tumorigenesis
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
Cell Cycle Control And Tumorigenesis, supplied by Proteos Inc, 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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DWK Life Sciences cell cycle control
Figure 4: Changes of <t>cdc2,</t> cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).
Cell Cycle Control, supplied by DWK Life Sciences, 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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Hartenstein GmbH zygotic cell cycle control
Summary, showing fluctuations in levels of String (bold line), Cyclin B (dashed line), and Cdc2 (fine line) during the first 14 <t>cell</t> cycles. Protein levels are depicted along the y-axis on a linear scale, with arbitrary units. Time is indicated along the x-axis, with periods of mitosis boxed in black and numbered. During cycles 1–7, there is little fluctuation in Cyclin levels or Cdc2 kinase activity. Beginning at <t>cycle</t> 8, Cyclin degradation at metaphase/anaphase transitions becomes apparent, and the cycles begin to slow. At this point Cdc2 kinase activity also begins to fluctuate, due to gain and loss of the activating phosphate at T161. It is note-worthy that greater amounts of Cyclin are degraded with progressively later cycles. Because nuclei and mitotic apparatuses (presumed Cdc2/Cyclin substrates) increase exponentially in number, this suggests a connection between Cyclin utilization and its degradation. Accordingly, we propose that cycle slowdown following mitosis 8 is effected by titration and depletion of maternal Cyclins (Table 1). Mitosis 14 is timed by a distinct mechanism, in which inactive Cdc2/Cyclin complexes are activated by String translated from new <t>zygotic</t> transcripts.
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Image Search Results


Impacts of Limonin upon FXR/FGF15 signaling pathway in intestinal of hyperlipidemia mice. ( A ) Representative picture of immunofluorescence expression in mice intestine. ( B ) The immunofluorescence protein expression of FGF15 in the ileum. ( C ) The immunofluorescence protein expression of FXR in the ileum. ( D ) Ileum mRNA expression levels of Fgf15 . ( E ) Ileum mRNA expression levels of Fxr . ( F ) Ileum mRNA expression levels of Asbt . ( G ) Representative protein bands detected by WB. ( H ) Ileum protein expression levels of FGF15. ( I ) Ileum protein expression levels of FXR. ( J ) Ileum protein expression levels of ASBT. Values are shown as mean ± SD ( n = 3). # P < 0.05, ## P < 0.01 vs. MG and * P < 0.05, ** P < 0.01 vs. NG

Journal: Journal of Translational Medicine

Article Title: Limonin attenuates hyperlipidemia by regulating the gut microbiota-bile acid-farnesoid X receptor axis

doi: 10.1186/s12967-026-07826-7

Figure Lengend Snippet: Impacts of Limonin upon FXR/FGF15 signaling pathway in intestinal of hyperlipidemia mice. ( A ) Representative picture of immunofluorescence expression in mice intestine. ( B ) The immunofluorescence protein expression of FGF15 in the ileum. ( C ) The immunofluorescence protein expression of FXR in the ileum. ( D ) Ileum mRNA expression levels of Fgf15 . ( E ) Ileum mRNA expression levels of Fxr . ( F ) Ileum mRNA expression levels of Asbt . ( G ) Representative protein bands detected by WB. ( H ) Ileum protein expression levels of FGF15. ( I ) Ileum protein expression levels of FXR. ( J ) Ileum protein expression levels of ASBT. Values are shown as mean ± SD ( n = 3). # P < 0.05, ## P < 0.01 vs. MG and * P < 0.05, ** P < 0.01 vs. NG

Article Snippet: The protein expression of FXR (BOSTER, M03308), FGF15 (Cohesion, CQA5895), ASBT (Cohesion, CQA5895), and FGFR4 (Cohesion, CPA9200) in the liver and ileum were detected by TSA multi-marker staining technique.

Techniques: Immunofluorescence, Expressing

Impacts of Limonin upon FXR/FGF15 signaling pathway in hyperlipidemia mice liver. ( A ) mRNA expression levels of fgf15 in liver. ( B ) mRNA expression levels of Fgfr4 in liver. ( C ) mRNA expression levels of Cyp7a1 in liver. ( D ) Representative picture of immunofluorescence expression in mice liver. ( E ) F Immunofluorescence expression of CYP7A1 in liver. ( F ) Immunofluorescence expression of CYP7A1 in liver. ( G ) Immunofluorescence expression of CYP7A1 in liver. ( H ) FGF15 protein expression levels. ( I ) FGFR4 protein expression levels. ( J ) CYP7A1 protein expression levels. ( K ) Representative protein bands detected by WB. Values are denoted by mean ± SD ( n = 3). # P < 0.05, ## P < 0.01 vs. MG and * P < 0.05, ** P < 0.01 vs. NG

Journal: Journal of Translational Medicine

Article Title: Limonin attenuates hyperlipidemia by regulating the gut microbiota-bile acid-farnesoid X receptor axis

doi: 10.1186/s12967-026-07826-7

Figure Lengend Snippet: Impacts of Limonin upon FXR/FGF15 signaling pathway in hyperlipidemia mice liver. ( A ) mRNA expression levels of fgf15 in liver. ( B ) mRNA expression levels of Fgfr4 in liver. ( C ) mRNA expression levels of Cyp7a1 in liver. ( D ) Representative picture of immunofluorescence expression in mice liver. ( E ) F Immunofluorescence expression of CYP7A1 in liver. ( F ) Immunofluorescence expression of CYP7A1 in liver. ( G ) Immunofluorescence expression of CYP7A1 in liver. ( H ) FGF15 protein expression levels. ( I ) FGFR4 protein expression levels. ( J ) CYP7A1 protein expression levels. ( K ) Representative protein bands detected by WB. Values are denoted by mean ± SD ( n = 3). # P < 0.05, ## P < 0.01 vs. MG and * P < 0.05, ** P < 0.01 vs. NG

Article Snippet: The protein expression of FXR (BOSTER, M03308), FGF15 (Cohesion, CQA5895), ASBT (Cohesion, CQA5895), and FGFR4 (Cohesion, CPA9200) in the liver and ileum were detected by TSA multi-marker staining technique.

Techniques: Expressing, Immunofluorescence

Graphical illustration of mechanism mediating anti-hyperlipidemia effects of Limonin. The possible mechanisms by which limonin alleviates dyslipidemia are as follows: (1) Reduced relative abundance of BSH-producing microbes induced by Limonin. (2) Boosted conjugated BAs, particularly TCA, T-αMCA, and T-βMCA acting in antagonistic manner on intestinal FXR, (3) The increased conjugated BAs boosted elimination of BAs via feces, and also as endogenous signaling molecules that inhibited activation of intestinal FXR causing FGF15’s reduced production in the distal ileum. (4) The FGF15 through the enterohepatic circulation to enter mice liver, and regulates liver CYP7A1 expression via negative feedback of FGF15-FGFR4 pathway to promoting the synthesis of TC to BA, thereby reducing TC

Journal: Journal of Translational Medicine

Article Title: Limonin attenuates hyperlipidemia by regulating the gut microbiota-bile acid-farnesoid X receptor axis

doi: 10.1186/s12967-026-07826-7

Figure Lengend Snippet: Graphical illustration of mechanism mediating anti-hyperlipidemia effects of Limonin. The possible mechanisms by which limonin alleviates dyslipidemia are as follows: (1) Reduced relative abundance of BSH-producing microbes induced by Limonin. (2) Boosted conjugated BAs, particularly TCA, T-αMCA, and T-βMCA acting in antagonistic manner on intestinal FXR, (3) The increased conjugated BAs boosted elimination of BAs via feces, and also as endogenous signaling molecules that inhibited activation of intestinal FXR causing FGF15’s reduced production in the distal ileum. (4) The FGF15 through the enterohepatic circulation to enter mice liver, and regulates liver CYP7A1 expression via negative feedback of FGF15-FGFR4 pathway to promoting the synthesis of TC to BA, thereby reducing TC

Article Snippet: The protein expression of FXR (BOSTER, M03308), FGF15 (Cohesion, CQA5895), ASBT (Cohesion, CQA5895), and FGFR4 (Cohesion, CPA9200) in the liver and ileum were detected by TSA multi-marker staining technique.

Techniques: Activation Assay, Expressing

Figure 4: Changes of cdc2, cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).

Journal: Oncotarget

Article Title: Dietary NiCl₂ causes G₂/M cell cycle arrest in the broiler's kidney.

doi: 10.18632/oncotarget.5934

Figure Lengend Snippet: Figure 4: Changes of cdc2, cyclinB and PCNA protein expression levels in the kidney at 42 days of age. (Immunohistochemistry, ×400).

Article Snippet: Table 1: Antibodies used in immunohitochemistry Name Company Cat# Dilution p-ATM Bioss, China bs-2272R 1:100 p-Chk1 Bioss, China bs-5251R 1:100 p-Chk2 Bioss, China bs-3721R 1:100 p53 Boster, China BM0101 1:100 p21 Boster, China BA0272 1:100 p-cdc25C Bioss, China bs-3482R 1:100 p-cdc2 Boster, China BM0027 1:100 cyclinB1 Bioss, China bs-0572R 1:100 PCNA Boster, China BM0104 1:100 Oncotarget35969www.impactjournals.com/oncotarget or P < 0.01) in the 900 mg/kg groups at 14 days of age and in the three NiCl2-treated groups from 28 to 42 days of age in comparison with those in the control group.

Techniques: Expressing, Immunohistochemistry

Figure 6: Changes of the mean density of cdc2, cyclinB and PCNA protein expression in the kidney. Data are presented with the mean ± standard deviation (n=5×5) *P<0.05, compared with the control group **P<0.01, compared with the control group.

Journal: Oncotarget

Article Title: Dietary NiCl₂ causes G₂/M cell cycle arrest in the broiler's kidney.

doi: 10.18632/oncotarget.5934

Figure Lengend Snippet: Figure 6: Changes of the mean density of cdc2, cyclinB and PCNA protein expression in the kidney. Data are presented with the mean ± standard deviation (n=5×5) *P<0.05, compared with the control group **P<0.01, compared with the control group.

Article Snippet: Table 1: Antibodies used in immunohitochemistry Name Company Cat# Dilution p-ATM Bioss, China bs-2272R 1:100 p-Chk1 Bioss, China bs-5251R 1:100 p-Chk2 Bioss, China bs-3721R 1:100 p53 Boster, China BM0101 1:100 p21 Boster, China BA0272 1:100 p-cdc25C Bioss, China bs-3482R 1:100 p-cdc2 Boster, China BM0027 1:100 cyclinB1 Bioss, China bs-0572R 1:100 PCNA Boster, China BM0104 1:100 Oncotarget35969www.impactjournals.com/oncotarget or P < 0.01) in the 900 mg/kg groups at 14 days of age and in the three NiCl2-treated groups from 28 to 42 days of age in comparison with those in the control group.

Techniques: Expressing, Standard Deviation, Control

Figure 8: Changes of cdc2, cyclinB and PCNA mRNA expression levels in the kidney. Data are presented with the mean ± standard deviation (n=5) *P<0.05, compared with the control group **P<0.01, compared with the control group.

Journal: Oncotarget

Article Title: Dietary NiCl₂ causes G₂/M cell cycle arrest in the broiler's kidney.

doi: 10.18632/oncotarget.5934

Figure Lengend Snippet: Figure 8: Changes of cdc2, cyclinB and PCNA mRNA expression levels in the kidney. Data are presented with the mean ± standard deviation (n=5) *P<0.05, compared with the control group **P<0.01, compared with the control group.

Article Snippet: Table 1: Antibodies used in immunohitochemistry Name Company Cat# Dilution p-ATM Bioss, China bs-2272R 1:100 p-Chk1 Bioss, China bs-5251R 1:100 p-Chk2 Bioss, China bs-3721R 1:100 p53 Boster, China BM0101 1:100 p21 Boster, China BA0272 1:100 p-cdc25C Bioss, China bs-3482R 1:100 p-cdc2 Boster, China BM0027 1:100 cyclinB1 Bioss, China bs-0572R 1:100 PCNA Boster, China BM0104 1:100 Oncotarget35969www.impactjournals.com/oncotarget or P < 0.01) in the 900 mg/kg groups at 14 days of age and in the three NiCl2-treated groups from 28 to 42 days of age in comparison with those in the control group.

Techniques: Expressing, Standard Deviation, Control

Summary, showing fluctuations in levels of String (bold line), Cyclin B (dashed line), and Cdc2 (fine line) during the first 14 cell cycles. Protein levels are depicted along the y-axis on a linear scale, with arbitrary units. Time is indicated along the x-axis, with periods of mitosis boxed in black and numbered. During cycles 1–7, there is little fluctuation in Cyclin levels or Cdc2 kinase activity. Beginning at cycle 8, Cyclin degradation at metaphase/anaphase transitions becomes apparent, and the cycles begin to slow. At this point Cdc2 kinase activity also begins to fluctuate, due to gain and loss of the activating phosphate at T161. It is note-worthy that greater amounts of Cyclin are degraded with progressively later cycles. Because nuclei and mitotic apparatuses (presumed Cdc2/Cyclin substrates) increase exponentially in number, this suggests a connection between Cyclin utilization and its degradation. Accordingly, we propose that cycle slowdown following mitosis 8 is effected by titration and depletion of maternal Cyclins (Table 1). Mitosis 14 is timed by a distinct mechanism, in which inactive Cdc2/Cyclin complexes are activated by String translated from new zygotic transcripts.

Journal: Genes & development

Article Title: Distinct molecular mechanisms regulate cell cycle timing at successive stages of Drosophila embryogenesis

doi:

Figure Lengend Snippet: Summary, showing fluctuations in levels of String (bold line), Cyclin B (dashed line), and Cdc2 (fine line) during the first 14 cell cycles. Protein levels are depicted along the y-axis on a linear scale, with arbitrary units. Time is indicated along the x-axis, with periods of mitosis boxed in black and numbered. During cycles 1–7, there is little fluctuation in Cyclin levels or Cdc2 kinase activity. Beginning at cycle 8, Cyclin degradation at metaphase/anaphase transitions becomes apparent, and the cycles begin to slow. At this point Cdc2 kinase activity also begins to fluctuate, due to gain and loss of the activating phosphate at T161. It is note-worthy that greater amounts of Cyclin are degraded with progressively later cycles. Because nuclei and mitotic apparatuses (presumed Cdc2/Cyclin substrates) increase exponentially in number, this suggests a connection between Cyclin utilization and its degradation. Accordingly, we propose that cycle slowdown following mitosis 8 is effected by titration and depletion of maternal Cyclins (Table 1). Mitosis 14 is timed by a distinct mechanism, in which inactive Cdc2/Cyclin complexes are activated by String translated from new zygotic transcripts.

Article Snippet: Zygotic cell cycle control begins during interphase 14, and a series of slower, spatially patterned, G 2 -regulated cell cycles follow ( Hartenstein and Campos-Ortega 1985 ; Foe 1989 ; Edgar and O’Farrell 1990 ).

Techniques: Activity Assay, Titration