fos b Search Results


anti fosb  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology anti fosb
Anti Fosb, 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
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fosb sc 35403 sirnas  (Santa Cruz Biotechnology)
85
Santa Cruz Biotechnology fosb sc 35403 sirnas
Fosb Sc 35403 Sirnas, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 85 stars, based on 1 article reviews
fosb sc 35403 sirnas - by Bioz Stars, 2026-04
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fosb  (OriGene)
94
OriGene fosb
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Fosb, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fosb/product/OriGene
Average 94 stars, based on 1 article reviews
fosb - by Bioz Stars, 2026-04
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sirna targeting fos  (Santa Cruz Biotechnology)
85
Santa Cruz Biotechnology sirna targeting fos
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Sirna Targeting Fos, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 85 stars, based on 1 article reviews
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fos b  (Santa Cruz Biotechnology)
86
Santa Cruz Biotechnology fos b
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Fos B, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fos-b stellaris fish probe set  (LGC Biosearch)
90
LGC Biosearch fos-b stellaris fish probe set
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Fos B Stellaris Fish Probe Set, supplied by LGC Biosearch, 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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fos and fosb genes  (Wolters Kluwer Health)
90
Wolters Kluwer Health fos and fosb genes
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Fos And Fosb Genes, supplied by Wolters Kluwer Health, 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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elisa kit trans am ap-1c-fos/fosb/c-jun/jun d  (Active Motif)
90
Active Motif elisa kit trans am ap-1c-fos/fosb/c-jun/jun d
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Elisa Kit Trans Am Ap 1c Fos/Fosb/C Jun/Jun D, supplied by Active Motif, 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/elisa kit trans am ap-1c-fos/fosb/c-jun/jun d/product/Active Motif
Average 90 stars, based on 1 article reviews
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fos (cfos, fosb, fra1, and fra2)  (Rauscher GmbH)
90
Rauscher GmbH fos (cfos, fosb, fra1, and fra2)
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Fos (Cfos, Fosb, Fra1, And Fra2), supplied by Rauscher GmbH, 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/fos (cfos, fosb, fra1, and fra2)/product/Rauscher GmbH
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antibodies fos b (sc-398595 x)  (Active Motif)
90
Active Motif antibodies fos b (sc-398595 x)
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Antibodies Fos B (Sc 398595 X), supplied by Active Motif, 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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antibodies against c-fos and fos-b proteins  (Kitayama Labes Co Ltd)
90
Kitayama Labes Co Ltd antibodies against c-fos and fos-b proteins
a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; <t>FosB;</t> Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: <t>c-Jun,</t> <t>JunB,</t> JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.
Antibodies Against C Fos And Fos B Proteins, supplied by Kitayama Labes Co 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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Image Search Results


a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; FosB; Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: c-Jun, JunB, JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.

Journal: medRxiv

Article Title: Allelic effects on KLHL17 expression likely mediated by JunB/D underlie a PDAC GWAS signal at chr1p36.33

doi: 10.1101/2024.09.16.24313748

Figure Lengend Snippet: a) in silico TF binding predictions; b) EMSA using TPA-stimulated nuclear HeLa extract and fluorescently labeled oligonucleotide. Arrow indicates the allele-preferential binding; c) Luciferase reporter assay using DMSO and TPA stimulation and the rs13303160 sequence as an enhancer in the PANC-1 cell line; luciferase activity reported relative to the Empty Vector (EV). Unpaired t-tests were performed on the relative luciferase activity of the A/G ratio compared to A/A; d) Representative EMSAs with increasing amounts of recombinant Fos proteins (from left to right: c-Fos; FosB; Fos1L; Fos2L); e) Representative EMSAs with increasing amounts of recombinant Jun proteins (from left to right: c-Jun, JunB, JunD). Arrow indicates the allele-specific binding; f, g) Supershift EMSA with antibodies against JunB and JunD respectively using both TPA-stimulated nuclear lysate and recombinant protein; Arrows denote the shift in the bands; h) ChIP-qPCR in SW1990 PDAC cells for JunB and JunD using 3 primer sets (PS) surrounding the SNP. Positive controls are from a JunB ChIP-seq performed in the CFPAC1 PDAC cell line. Negative control is from a quiescent region on 1p36.33; i) TaqMan genotyping assay for rs13303160 using immunoprecipitated DNA from the ChIP. The ratio of A to G was determined relative to the quantity of A and G alleles in the input DNA. For all graphs, error bars represent the SEM. Unpaired two-tailed t-tests were performed; * P <0.05; ** P <0.01; *** P <0.001.

Article Snippet: Recombinant ELF1 (TP760629), ELF2 (TP760288), ELF3 (TP300631), ELF4 (TP761826), JUNB (TP303595), JUND (TP316958 4), c-FOS (TP760257), FOS1L (TP302104), FOSB (TP762032), FOS2L (TP760114) protein were purchased from Origene (Rockville, MD). c-JUN was purchased from Abcam (Waltham, MA) (ab84134).

Techniques: In Silico, Binding Assay, Labeling, Luciferase, Reporter Assay, Sequencing, Activity Assay, Plasmid Preparation, Recombinant, ChIP-sequencing, Negative Control, Genotyping Assay, Immunoprecipitation, Two Tailed Test