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anti pgc 1α rabbit polyclonal  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology anti pgc 1α rabbit polyclonal
    Anti Pgc 1α Rabbit Polyclonal, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 530 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+rap1+antibody/RAP1+Antibody/pm41661273-70-24-27
    Average 94 stars, based on 530 article reviews
    anti pgc 1α rabbit polyclonal - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Incubation:

    Article Title: Ras guanyl nucleotide releasing protein 2 affects cell viability and cell-matrix adhesion in ECV304 endothelial cells.
    Article Snippet: Membranes were blocked for 30 min by using the PVDF blocking reagent for Can Get Signal® (Toyobo). .. After washing with PBS containing 0.05% Tween 20 (PBS-T), the membranes were incubated with rabbit anti-RasGRP2 antibody (GeneTex), mouse anti-β-actin antibody, rabbit anti-Rap1 antibody (Santa Cruz), mouse antipan-Ras antibody (Cell Biolabs), rabbit anti-phospho-p44/42 MAPK antibody, or rabbit anti-p44/42 MAPK antibody (Cell Signaling) in Can Get Signal® Solution 1 (Toyobo) for 1 h. Subsequently, the membranes were washed thrice with PBS-T and incubated with anti-rabbit IgG antibody (GeneTex) or antimouse IgG antibody (DakoCytomation) in Can Get Signal® Solution 2 (Toyobo) for 1 h. After five additional washes with PBS-T, immunoreactive proteins were detected using ECL Prime Western Blotting Detection Reagents and Amersham hyperfilmTM ECL (GE Healthcare). ..

    Article Title: Ras guanyl nucleotide releasing protein 2 affects cell viability and cell-matrix adhesion in ECV304 endothelial cells
    Article Snippet: Membranes were blocked for 30 min by using the PVDF blocking reagent for Can Get Signal ® (Toyobo). .. After washing with PBS containing 0.05% Tween 20 (PBS-T), the membranes were incubated with rabbit anti-RasGRP2 antibody (GeneTex), mouse anti-β-actin antibody, rabbit anti-Rap1 antibody (Santa Cruz), mouse anti-pan-Ras antibody (Cell Biolabs), rabbit anti-phospho-p44/42 MAPK antibody, or rabbit anti-p44/42 MAPK antibody (Cell Signaling) in Can Get Signal ® Solution 1 (Toyobo) for 1 h. Subsequently, the membranes were washed thrice with PBS-T and incubated with anti-rabbit IgG antibody (GeneTex) or anti-mouse IgG antibody (DakoCytomation) in Can Get Signal ® Solution 2 (Toyobo) for 1 h. After five additional washes with PBS-T, immunoreactive proteins were detected using ECL Prime Western Blotting Detection Reagents and Amersham hyperfilm TM ECL (GE Healthcare). .. Ras and Rap1 activity assay Ras activation was examined using the pan-Ras activation assay kit (Cell Biolabs).

    Article Title: RASGRP2 Suppresses Apoptosis via Inhibition of ROS Production in Vascular Endothelial Cells
    Article Snippet: Membranes were blocked for 30 min using the PVDF blocking agent for Can Get Signal® (Toyobo, Tokyo, Japan). .. After washing with PBS containing 0.05% Tween 20 (PBS-T), the membranes were incubated with rabbit anti-RASGRP2 antibody (GeneTex, Irvine, California, USA), mouse anti- β -actin antibody (Santa Cruz, USA), rabbit anti-NOX4 antibody (GeneTex), or rabbit anti-Rap1 antibody (Santa Cruz) in Can Get Signal® Solution 1 (Toyobo) for 1 h. Subsequently, the membranes were washed thrice with PBS-T and incubated with anti-rabbit IgG antibody (GeneTex) or anti-mouse IgG antibody (Dako-cytomation, USA) in Can Get Signal® Solution 2 (Toyobo) for 1 h. After five additional washes with PBS-T, immunoreactive proteins were detected using ECL Prime Western Blotting Detection Reagents and Amersham HyperfilmTM ECL (GE HealthCare, NJ, USA). .. Rap1 activity was examined using RalGDS-RBD Agarose Beads (Cell Biolabs, San Diego, CA).

    Western Blot:

    Article Title: Ras guanyl nucleotide releasing protein 2 affects cell viability and cell-matrix adhesion in ECV304 endothelial cells.
    Article Snippet: Membranes were blocked for 30 min by using the PVDF blocking reagent for Can Get Signal® (Toyobo). .. After washing with PBS containing 0.05% Tween 20 (PBS-T), the membranes were incubated with rabbit anti-RasGRP2 antibody (GeneTex), mouse anti-β-actin antibody, rabbit anti-Rap1 antibody (Santa Cruz), mouse antipan-Ras antibody (Cell Biolabs), rabbit anti-phospho-p44/42 MAPK antibody, or rabbit anti-p44/42 MAPK antibody (Cell Signaling) in Can Get Signal® Solution 1 (Toyobo) for 1 h. Subsequently, the membranes were washed thrice with PBS-T and incubated with anti-rabbit IgG antibody (GeneTex) or antimouse IgG antibody (DakoCytomation) in Can Get Signal® Solution 2 (Toyobo) for 1 h. After five additional washes with PBS-T, immunoreactive proteins were detected using ECL Prime Western Blotting Detection Reagents and Amersham hyperfilmTM ECL (GE Healthcare). ..

    Article Title: Ras guanyl nucleotide releasing protein 2 affects cell viability and cell-matrix adhesion in ECV304 endothelial cells
    Article Snippet: Membranes were blocked for 30 min by using the PVDF blocking reagent for Can Get Signal ® (Toyobo). .. After washing with PBS containing 0.05% Tween 20 (PBS-T), the membranes were incubated with rabbit anti-RasGRP2 antibody (GeneTex), mouse anti-β-actin antibody, rabbit anti-Rap1 antibody (Santa Cruz), mouse anti-pan-Ras antibody (Cell Biolabs), rabbit anti-phospho-p44/42 MAPK antibody, or rabbit anti-p44/42 MAPK antibody (Cell Signaling) in Can Get Signal ® Solution 1 (Toyobo) for 1 h. Subsequently, the membranes were washed thrice with PBS-T and incubated with anti-rabbit IgG antibody (GeneTex) or anti-mouse IgG antibody (DakoCytomation) in Can Get Signal ® Solution 2 (Toyobo) for 1 h. After five additional washes with PBS-T, immunoreactive proteins were detected using ECL Prime Western Blotting Detection Reagents and Amersham hyperfilm TM ECL (GE Healthcare). .. Ras and Rap1 activity assay Ras activation was examined using the pan-Ras activation assay kit (Cell Biolabs).

    Article Title: RASGRP2 Suppresses Apoptosis via Inhibition of ROS Production in Vascular Endothelial Cells
    Article Snippet: Membranes were blocked for 30 min using the PVDF blocking agent for Can Get Signal® (Toyobo, Tokyo, Japan). .. After washing with PBS containing 0.05% Tween 20 (PBS-T), the membranes were incubated with rabbit anti-RASGRP2 antibody (GeneTex, Irvine, California, USA), mouse anti- β -actin antibody (Santa Cruz, USA), rabbit anti-NOX4 antibody (GeneTex), or rabbit anti-Rap1 antibody (Santa Cruz) in Can Get Signal® Solution 1 (Toyobo) for 1 h. Subsequently, the membranes were washed thrice with PBS-T and incubated with anti-rabbit IgG antibody (GeneTex) or anti-mouse IgG antibody (Dako-cytomation, USA) in Can Get Signal® Solution 2 (Toyobo) for 1 h. After five additional washes with PBS-T, immunoreactive proteins were detected using ECL Prime Western Blotting Detection Reagents and Amersham HyperfilmTM ECL (GE HealthCare, NJ, USA). .. Rap1 activity was examined using RalGDS-RBD Agarose Beads (Cell Biolabs, San Diego, CA).

    Double Immunofluorescence Staining:

    Article Title: Rap1 induces cytokine production in pro-inflammatory macrophages through NFκB signaling and is highly expressed in human atherosclerotic lesions
    Article Snippet: .. For the localization of Rap1 to respective cell types, double immunofluorescence staining was performed using rabbit anti-Rap1 antibody (Santa Cruz, CA, USA) mixed with cell selective monoclonal antibodies: mouse anti-CD68 (macrophages, Dako), or CD31 (endothelial cells, Dako), or HHF35 (smooth muscle cells, Enzo Life Sciences). .. Subsequently, a mixture of secondary antibodies goat anti-rabbit Alexa 555 (red, Cat. no. A-21428, Invitrogen) and goat anti-mouse Alexa 488 (green, Cat. no. A-11029, Invitrogen) was applied to visualize antigens.

    other:

    Article Title: Rap1 induces cytokine production in pro-inflammatory macrophages through NFκB signaling and is highly expressed in human atherosclerotic lesions
    Article Snippet: Subsequently, a mixture of secondary antibodies goat anti-rabbit Alexa 555 (red, Cat. no. A-21428, Invitrogen) and goat anti-mouse Alexa 488 (green, Cat. no. A-11029, Invitrogen) was applied to visualize antigens.



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    Information of primary antibodies used in the present study.
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    Image Search Results


    Information of primary antibodies used in the present study.

    Journal: Scientific Reports

    Article Title: CD147 regulates the Rap1 signaling pathway to promote proliferation, migration, and invasion, and inhibit apoptosis in colorectal cancer cells

    doi: 10.1038/s41598-025-98266-8

    Figure Lengend Snippet: Information of primary antibodies used in the present study.

    Article Snippet: Anti RAP1 rabbit polyclonal antibody , 14595-1-AP , ProteinTech Group, Inc. , 1:1000.

    Techniques:

    Primer sequence and promoter primer sequence.

    Journal: Scientific Reports

    Article Title: CD147 regulates the Rap1 signaling pathway to promote proliferation, migration, and invasion, and inhibit apoptosis in colorectal cancer cells

    doi: 10.1038/s41598-025-98266-8

    Figure Lengend Snippet: Primer sequence and promoter primer sequence.

    Article Snippet: Anti RAP1 rabbit polyclonal antibody , 14595-1-AP , ProteinTech Group, Inc. , 1:1000.

    Techniques: Sequencing

    CD147 overexpression correlates with poor prognosis and RAP1 co-expression in colorectal cancer. ( A , B ) CD147 mRNA expression levels in tumor vs. normal tissues across multiple cancers (UCSC Xena database) and specifically in colorectal cancer (CRC) (GEPIA database). ** P < 0.01, unpaired t-test. ( C ) Kaplan-Meier survival analysis of CRC patients stratified by CD147 expression (log-rank test, P < 0.05). ( D ) Representative immunohistochemical images from The Human Protein Atlas showing CD147 expression in normal colorectal tissue (negative) and CRC tissue (cytoplasmic/membrane staining). ( E , F ) Western blot analysis of CD147 protein levels in paired CRC and adjacent normal tissues ( n = 12). β-actin served as loading control. *** P < 0.001, paired t-test. Origin blots are presented in Supplementary Fig. 1. ( G , H ) Correlation analyses between CD147 and RAP1A/B mRNA expression using GEPIA (Pearson’s correlation, P < 0.05) and TIMER2.0 (no significant correlation). ( I ) qRT-PCR validation of CD147 and Rap1 expression correlation in 12 CRC tissues (Pearson’s correlation, P < 0.01).

    Journal: Scientific Reports

    Article Title: CD147 regulates the Rap1 signaling pathway to promote proliferation, migration, and invasion, and inhibit apoptosis in colorectal cancer cells

    doi: 10.1038/s41598-025-98266-8

    Figure Lengend Snippet: CD147 overexpression correlates with poor prognosis and RAP1 co-expression in colorectal cancer. ( A , B ) CD147 mRNA expression levels in tumor vs. normal tissues across multiple cancers (UCSC Xena database) and specifically in colorectal cancer (CRC) (GEPIA database). ** P < 0.01, unpaired t-test. ( C ) Kaplan-Meier survival analysis of CRC patients stratified by CD147 expression (log-rank test, P < 0.05). ( D ) Representative immunohistochemical images from The Human Protein Atlas showing CD147 expression in normal colorectal tissue (negative) and CRC tissue (cytoplasmic/membrane staining). ( E , F ) Western blot analysis of CD147 protein levels in paired CRC and adjacent normal tissues ( n = 12). β-actin served as loading control. *** P < 0.001, paired t-test. Origin blots are presented in Supplementary Fig. 1. ( G , H ) Correlation analyses between CD147 and RAP1A/B mRNA expression using GEPIA (Pearson’s correlation, P < 0.05) and TIMER2.0 (no significant correlation). ( I ) qRT-PCR validation of CD147 and Rap1 expression correlation in 12 CRC tissues (Pearson’s correlation, P < 0.01).

    Article Snippet: Anti RAP1 rabbit polyclonal antibody , 14595-1-AP , ProteinTech Group, Inc. , 1:1000.

    Techniques: Over Expression, Expressing, Immunohistochemical staining, Membrane, Staining, Western Blot, Control, Quantitative RT-PCR, Biomarker Discovery

    Rap1 overexpression reverses the expression of key proteins in CD147 knockdown mediated cell proliferation, apoptosis and EMT. ( A , B ) Western blot analysis of Rap1 and Rap1GAP protein levels in HCT116 and SW620 cells after CD147 knockdown (shCD147). β-actin served as a loading control. Data represent mean ± SD ( n = 3; ** P < 0.01, *** P < 0.001 vs. shNC, Student’s t-test). Original blots are presented in Supplementary Fig. 3. ( C ) qRT-PCR validation of Rap1 mRNA overexpression in CD147-knockdown cells. Expression normalized to β-actin ( n = 3; *** P < 0.001 vs. HCT116 or SW620, Student’s t-test). ( D , E ) Western blot analysis of c-Myc, Bcl-2, Bax, N-cadherin, and E-cadherin protein levels in CD147-Knockdown cells with Rap1 overexpression ( n = 3; * P < 0.05, ** P < 0.01, *** P < 0.001 vs. shNC, # P < 0.05, ## P < 0.01, ### P < 0.001 vs. shCD147, one-way ANOVA). Original blots are presented in Supplementary Fig. 4.

    Journal: Scientific Reports

    Article Title: CD147 regulates the Rap1 signaling pathway to promote proliferation, migration, and invasion, and inhibit apoptosis in colorectal cancer cells

    doi: 10.1038/s41598-025-98266-8

    Figure Lengend Snippet: Rap1 overexpression reverses the expression of key proteins in CD147 knockdown mediated cell proliferation, apoptosis and EMT. ( A , B ) Western blot analysis of Rap1 and Rap1GAP protein levels in HCT116 and SW620 cells after CD147 knockdown (shCD147). β-actin served as a loading control. Data represent mean ± SD ( n = 3; ** P < 0.01, *** P < 0.001 vs. shNC, Student’s t-test). Original blots are presented in Supplementary Fig. 3. ( C ) qRT-PCR validation of Rap1 mRNA overexpression in CD147-knockdown cells. Expression normalized to β-actin ( n = 3; *** P < 0.001 vs. HCT116 or SW620, Student’s t-test). ( D , E ) Western blot analysis of c-Myc, Bcl-2, Bax, N-cadherin, and E-cadherin protein levels in CD147-Knockdown cells with Rap1 overexpression ( n = 3; * P < 0.05, ** P < 0.01, *** P < 0.001 vs. shNC, # P < 0.05, ## P < 0.01, ### P < 0.001 vs. shCD147, one-way ANOVA). Original blots are presented in Supplementary Fig. 4.

    Article Snippet: Anti RAP1 rabbit polyclonal antibody , 14595-1-AP , ProteinTech Group, Inc. , 1:1000.

    Techniques: Over Expression, Expressing, Knockdown, Western Blot, Control, Quantitative RT-PCR, Biomarker Discovery

    Rap1 overexpression rescues the regulatory effects of CD147 knockdown on proliferation and apoptosis. ( A ) CCK-8 assay showing proliferation of HCT116 ( n = 3; *** P < 0.001 vs. shNC, ### P < 0.001 vs. shCD147, one-way ANOVA). ( B , C ) Colony formation assays in HCT116 cells. Colonies were counted and normalized to shCtrl ( n = 3; ** P < 0.01, *** P < 0.001 vs. shNC, ### P < 0.001 vs. shCD147, one-way ANOVA). ( D , E ) Flow cytometry analysis of apoptosis in HCT116 cells. Percentages of apoptotic cells are shown ( n = 3; * P < 0.05 vs. shNC, # P < 0.05 vs. shCD147, one-way ANOVA). Similar results were observed in SW620 cells.

    Journal: Scientific Reports

    Article Title: CD147 regulates the Rap1 signaling pathway to promote proliferation, migration, and invasion, and inhibit apoptosis in colorectal cancer cells

    doi: 10.1038/s41598-025-98266-8

    Figure Lengend Snippet: Rap1 overexpression rescues the regulatory effects of CD147 knockdown on proliferation and apoptosis. ( A ) CCK-8 assay showing proliferation of HCT116 ( n = 3; *** P < 0.001 vs. shNC, ### P < 0.001 vs. shCD147, one-way ANOVA). ( B , C ) Colony formation assays in HCT116 cells. Colonies were counted and normalized to shCtrl ( n = 3; ** P < 0.01, *** P < 0.001 vs. shNC, ### P < 0.001 vs. shCD147, one-way ANOVA). ( D , E ) Flow cytometry analysis of apoptosis in HCT116 cells. Percentages of apoptotic cells are shown ( n = 3; * P < 0.05 vs. shNC, # P < 0.05 vs. shCD147, one-way ANOVA). Similar results were observed in SW620 cells.

    Article Snippet: Anti RAP1 rabbit polyclonal antibody , 14595-1-AP , ProteinTech Group, Inc. , 1:1000.

    Techniques: Over Expression, Knockdown, CCK-8 Assay, Flow Cytometry

    Rap1 restores CD147-mediated migration and invasion in colorectal cancer cells. ( A , C ) Scratch wound healing assay in HCT116 cells. Healing rates were quantified at 24 h and 48 h ( n = 3; *** P < 0.001 vs. shNC, ## P < 0.01, ### P < 0.001 vs. shCD147, one-way ANOVA). ( B , D ) Transwell migration and Matrigel invasion assays. Migrated/invaded cells were counted and normalized to shCtrl ( n = 3; *** P < 0.001 vs. shNC, ### P < 0.001 vs. shCD147, one-way ANOVA). SW620 cells showed consistent trends. ( E ) Mechanistic diagram of CD147 promoting tumor progression through Rap1/Rap1GAP signaling in colorectal cancer cells.

    Journal: Scientific Reports

    Article Title: CD147 regulates the Rap1 signaling pathway to promote proliferation, migration, and invasion, and inhibit apoptosis in colorectal cancer cells

    doi: 10.1038/s41598-025-98266-8

    Figure Lengend Snippet: Rap1 restores CD147-mediated migration and invasion in colorectal cancer cells. ( A , C ) Scratch wound healing assay in HCT116 cells. Healing rates were quantified at 24 h and 48 h ( n = 3; *** P < 0.001 vs. shNC, ## P < 0.01, ### P < 0.001 vs. shCD147, one-way ANOVA). ( B , D ) Transwell migration and Matrigel invasion assays. Migrated/invaded cells were counted and normalized to shCtrl ( n = 3; *** P < 0.001 vs. shNC, ### P < 0.001 vs. shCD147, one-way ANOVA). SW620 cells showed consistent trends. ( E ) Mechanistic diagram of CD147 promoting tumor progression through Rap1/Rap1GAP signaling in colorectal cancer cells.

    Article Snippet: Anti RAP1 rabbit polyclonal antibody , 14595-1-AP , ProteinTech Group, Inc. , 1:1000.

    Techniques: Migration, Wound Healing Assay