anti-rap 1a Search Results


90
Danaher Inc rap-1a antibody
Rap 1a Antibody, supplied by Danaher 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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Santa Cruz Biotechnology anti ras related protein 1a rap1a
Toxicity of ARC39 in vitro. (A, B) L929 and HepG2 cells were treated with ARC39 as indicated. A: After 24 h treatment, cells were stained with annexin V/PI and analyzed by flow cytometry. B: After 24 and 48 h treatment, cell viability was determined with XTT reduction assay. C, D: Unprenylated <t>Rap1A</t> and RAP1A protein, respectively, normalized to β-actin in L929 and HepG2 cells, respectively, after 24 h treatment with ARC39 with representative Western blots. Zoledronate served as a positive control. Control values are normalized to their mean. Data are represented as mean ± SD, n = 3–4 experiments. One-way ANOVA was used in A, C, and D and two-way ANOVA in B, both followed by Bonferroni correction. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.
Anti Ras Related Protein 1a Rap1a, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti ras related protein 1a rap1a/product/Santa Cruz Biotechnology
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90
GenScript corporation antirap 1a/b rabbit polyclonal antibodies
Toxicity of ARC39 in vitro. (A, B) L929 and HepG2 cells were treated with ARC39 as indicated. A: After 24 h treatment, cells were stained with annexin V/PI and analyzed by flow cytometry. B: After 24 and 48 h treatment, cell viability was determined with XTT reduction assay. C, D: Unprenylated <t>Rap1A</t> and RAP1A protein, respectively, normalized to β-actin in L929 and HepG2 cells, respectively, after 24 h treatment with ARC39 with representative Western blots. Zoledronate served as a positive control. Control values are normalized to their mean. Data are represented as mean ± SD, n = 3–4 experiments. One-way ANOVA was used in A, C, and D and two-way ANOVA in B, both followed by Bonferroni correction. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.
Antirap 1a/B Rabbit Polyclonal Antibodies, supplied by GenScript corporation, 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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Becton Dickinson mouse anti-ras-related protein rap 1a
Toxicity of ARC39 in vitro. (A, B) L929 and HepG2 cells were treated with ARC39 as indicated. A: After 24 h treatment, cells were stained with annexin V/PI and analyzed by flow cytometry. B: After 24 and 48 h treatment, cell viability was determined with XTT reduction assay. C, D: Unprenylated <t>Rap1A</t> and RAP1A protein, respectively, normalized to β-actin in L929 and HepG2 cells, respectively, after 24 h treatment with ARC39 with representative Western blots. Zoledronate served as a positive control. Control values are normalized to their mean. Data are represented as mean ± SD, n = 3–4 experiments. One-way ANOVA was used in A, C, and D and two-way ANOVA in B, both followed by Bonferroni correction. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.
Mouse Anti Ras Related Protein Rap 1a, supplied by Becton Dickinson, 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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Average 90 stars, based on 1 article reviews
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90
Santa Cruz Biotechnology goat anti-rap1a (c-17 - epitope mapping at the c-terminus of rap 1a of human origin)
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Goat Anti Rap1a (C 17 Epitope Mapping At The C Terminus Of Rap 1a Of Human Origin), supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/goat anti-rap1a (c-17 - epitope mapping at the c-terminus of rap 1a of human origin)/product/Santa Cruz Biotechnology
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90
GenScript corporation anti-rap 1a/b rabbit polyclonal antibodies
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Anti Rap 1a/B Rabbit Polyclonal Antibodies, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-rap 1a/b rabbit polyclonal antibodies/product/GenScript corporation
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Santa Cruz Biotechnology anti-rap 1a antibody detects total rap 1a
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Anti Rap 1a Antibody Detects Total Rap 1a, supplied by Santa Cruz Biotechnology, 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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96
Santa Cruz Biotechnology anti rap 1a sc 1482 antiserum
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Anti Rap 1a Sc 1482 Antiserum, supplied by Santa Cruz Biotechnology, 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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90
Santa Cruz Biotechnology rabbit antirat srebp-1c polyclonal antibody
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Rabbit Antirat Srebp 1c Polyclonal Antibody, supplied by Santa Cruz Biotechnology, 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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Santa Cruz Biotechnology goat polyclonal anti-rap 1a (c17
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Goat Polyclonal Anti Rap 1a (C17, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/goat polyclonal anti-rap 1a (c17/product/Santa Cruz Biotechnology
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90
Cell Signaling Technology Inc rap 1a/b antibody
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Rap 1a/B Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rap 1a/b antibody/product/Cell Signaling Technology Inc
Average 90 stars, based on 1 article reviews
rap 1a/b antibody - by Bioz Stars, 2026-03
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90
Santa Cruz Biotechnology anti-rap 1a-c17
N-BP-induced accumulation of unprenylated <t>Rap1A</t> and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.
Anti Rap 1a C17, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-rap 1a-c17/product/Santa Cruz Biotechnology
Average 90 stars, based on 1 article reviews
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Image Search Results


Toxicity of ARC39 in vitro. (A, B) L929 and HepG2 cells were treated with ARC39 as indicated. A: After 24 h treatment, cells were stained with annexin V/PI and analyzed by flow cytometry. B: After 24 and 48 h treatment, cell viability was determined with XTT reduction assay. C, D: Unprenylated Rap1A and RAP1A protein, respectively, normalized to β-actin in L929 and HepG2 cells, respectively, after 24 h treatment with ARC39 with representative Western blots. Zoledronate served as a positive control. Control values are normalized to their mean. Data are represented as mean ± SD, n = 3–4 experiments. One-way ANOVA was used in A, C, and D and two-way ANOVA in B, both followed by Bonferroni correction. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.

Journal: Journal of Lipid Research

Article Title: Characterization of the small molecule ARC39, a direct and specific inhibitor of acid sphingomyelinase in vitro [S]

doi: 10.1194/jlr.RA120000682

Figure Lengend Snippet: Toxicity of ARC39 in vitro. (A, B) L929 and HepG2 cells were treated with ARC39 as indicated. A: After 24 h treatment, cells were stained with annexin V/PI and analyzed by flow cytometry. B: After 24 and 48 h treatment, cell viability was determined with XTT reduction assay. C, D: Unprenylated Rap1A and RAP1A protein, respectively, normalized to β-actin in L929 and HepG2 cells, respectively, after 24 h treatment with ARC39 with representative Western blots. Zoledronate served as a positive control. Control values are normalized to their mean. Data are represented as mean ± SD, n = 3–4 experiments. One-way ANOVA was used in A, C, and D and two-way ANOVA in B, both followed by Bonferroni correction. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.

Article Snippet: Proteins were transferred to nitrocellulose membranes blocked 1 h with StartingBlock blocking buffer (Thermo Fisher) and incubated with the appropriate primary antibody overnight at 4°C: anti-AC (4741, ProSci, 1:1,000), anti-ASM (AF5348, R&D, 1:50), anti-Ras-related protein 1A (RAP1A) (398755, Santa Cruz, 1:200), anti-β-actin (4778, Santa Cruz, 1:100,000), and subsequently secondary HRP- or AP-conjugated anti-rabbit or anti-mouse antibodies.

Techniques: In Vitro, Staining, Flow Cytometry, Western Blot, Positive Control, Control

N-BP-induced accumulation of unprenylated Rap1A and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.

Journal: Genome Biology

Article Title: Identification of secondary targets of N-containing bisphosphonates in mammalian cells via parallel competition analysis of the barcoded yeast deletion collection

doi: 10.1186/gb-2009-10-9-r93

Figure Lengend Snippet: N-BP-induced accumulation of unprenylated Rap1A and increase of DBF4, but not of TBCB, can be reversed by GGPP. Western blot (WB) analysis of MCF-7 cells treated with 10 -4 M ALE alone or in combination with 25 μM GGPP. The same volume of absolute ethanol was used as control vehicle of GGPP (Ctrl). Actin was used to show equal loading of the lanes.

Article Snippet: Blots were incubated with the following polyclonal antibodies: rabbit anti-Dbf4 (Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA), rabbit anti-actin (Sigma), goat anti-Rap1A (C-17 - epitope mapping at the C-terminus of Rap 1A of human origin), and rabbit anti-Rap1 (121 - epitope mapping near the C-terminus of Rap 1 of human origin) (Santa Cruz Biotechnology), and anti-TBCB, a generous gift of JC Zabala, Universidad de Cantabria, Santander, Spain.

Techniques: Western Blot