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Addgene inc xbai site
Xbai Site, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/starr+seq+vector/STARR-seq+luciferase+validation+vector_ORI_empty+(Plasmid+%2399297)/pmc12780183-479-8-11
Average 93 stars, based on 8 article reviews
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Related Articles

Luciferase:

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model.
Article Snippet: .. The STARR-seq luciferase reporter plasmid (vector_ORI_empty) was a gift from Alexander Stark (Addgene plasmid #99297; https://www.addgene.org/99297; RRID: Addgene_992927) 64. ..

Article Title: The non-canonical poly(A) polymerase FAM46C promotes erythropoiesis.
Article Snippet: The post-transcriptional regulation of mRNA is a crucial component of gene expression.. The disruption of this process has detrimental effects on the normal development and gives rise to various diseases.. Searching for novel post-transcriptional regulators and exploring their roles are essential for understanding development and disease.

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model
Article Snippet: .. The STARR-seq luciferase reporter plasmid (vector_ORI_empty) was a gift from Alexander Stark (Addgene plasmid #99297; https://www.addgene.org/99297 ; RRID: Addgene_992927) . ..

Article Title: Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma
Article Snippet: .. Enhancers were PCR-cloned from genomic DNA into the STARR-seq firefly luciferase validation vector ORI_empty (RRID: Addgene_99297). .. Vectors ORI_SV40 (RRID: Addgene_99309) and ORI_neg.cont (RRID: Addgene_99315) were used as positive and negative controls.

Article Title: Dynamic HSF2 regulation drives breast cancer progression by steering the balance between proliferation and invasion
Article Snippet: Following two weeks of culturing, the negative lentiviral status was confirmed for each cell line using the HIV-1 p24 DuoSet ELISA rom kit (DY7360-05, R&D Systems). .. The plasmids used for the luciferase assay were generated by cloning 1 kb of either the human HSF2 promoter or MMP9 promoter upstream of the respective TSS into a STARR-seq luciferase validation vector_ORI_empty vector (#99297, Addgene). ..

Plasmid Preparation:

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model.
Article Snippet: .. The STARR-seq luciferase reporter plasmid (vector_ORI_empty) was a gift from Alexander Stark (Addgene plasmid #99297; https://www.addgene.org/99297; RRID: Addgene_992927) 64. ..

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model
Article Snippet: .. The STARR-seq luciferase reporter plasmid (vector_ORI_empty) was a gift from Alexander Stark (Addgene plasmid #99297; https://www.addgene.org/99297 ; RRID: Addgene_992927) . ..

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model
Article Snippet: .. The 11X EBV TR was cloned into the XbaI site of Addgene #99297 plasmid using T4 DNA ligase (NEB, Cat. No. M0202). ..

Article Title: Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma
Article Snippet: .. Enhancers were PCR-cloned from genomic DNA into the STARR-seq firefly luciferase validation vector ORI_empty (RRID: Addgene_99297). .. Vectors ORI_SV40 (RRID: Addgene_99309) and ORI_neg.cont (RRID: Addgene_99315) were used as positive and negative controls.

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model.
Article Snippet: .. The 11X EBV TR was cloned into the XbaI site of Addgene #99297 plasmid using T4 DNA ligase (NEB, Cat. No. M0202). ..

Article Title: Dynamic HSF2 regulation drives breast cancer progression by steering the balance between proliferation and invasion
Article Snippet: Following two weeks of culturing, the negative lentiviral status was confirmed for each cell line using the HIV-1 p24 DuoSet ELISA rom kit (DY7360-05, R&D Systems). .. The plasmids used for the luciferase assay were generated by cloning 1 kb of either the human HSF2 promoter or MMP9 promoter upstream of the respective TSS into a STARR-seq luciferase validation vector_ORI_empty vector (#99297, Addgene). ..

other:

Article Title: Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma
Article Snippet: Vectors ORI_SV40 (RRID: Addgene_99309) and ORI_neg.cont (RRID: Addgene_99315) were used as positive and negative controls.

Polymerase Chain Reaction:

Article Title: The non-canonical poly(A) polymerase FAM46C promotes erythropoiesis.
Article Snippet: The post-transcriptional regulation of mRNA is a crucial component of gene expression.. The disruption of this process has detrimental effects on the normal development and gives rise to various diseases.. Searching for novel post-transcriptional regulators and exploring their roles are essential for understanding development and disease.

Article Title: Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma
Article Snippet: .. Enhancers were PCR-cloned from genomic DNA into the STARR-seq firefly luciferase validation vector ORI_empty (RRID: Addgene_99297). .. Vectors ORI_SV40 (RRID: Addgene_99309) and ORI_neg.cont (RRID: Addgene_99315) were used as positive and negative controls.

Cloning:

Article Title: The non-canonical poly(A) polymerase FAM46C promotes erythropoiesis.
Article Snippet: The post-transcriptional regulation of mRNA is a crucial component of gene expression.. The disruption of this process has detrimental effects on the normal development and gives rise to various diseases.. Searching for novel post-transcriptional regulators and exploring their roles are essential for understanding development and disease.

Article Title: Dynamic HSF2 regulation drives breast cancer progression by steering the balance between proliferation and invasion
Article Snippet: Following two weeks of culturing, the negative lentiviral status was confirmed for each cell line using the HIV-1 p24 DuoSet ELISA rom kit (DY7360-05, R&D Systems). .. The plasmids used for the luciferase assay were generated by cloning 1 kb of either the human HSF2 promoter or MMP9 promoter upstream of the respective TSS into a STARR-seq luciferase validation vector_ORI_empty vector (#99297, Addgene). ..

Clone Assay:

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model
Article Snippet: .. The 11X EBV TR was cloned into the XbaI site of Addgene #99297 plasmid using T4 DNA ligase (NEB, Cat. No. M0202). ..

Article Title: Discovering the complete enhancer map of human herpesviruses using a natural language processing model.
Article Snippet: .. The 11X EBV TR was cloned into the XbaI site of Addgene #99297 plasmid using T4 DNA ligase (NEB, Cat. No. M0202). ..

Biomarker Discovery:

Article Title: Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma
Article Snippet: .. Enhancers were PCR-cloned from genomic DNA into the STARR-seq firefly luciferase validation vector ORI_empty (RRID: Addgene_99297). .. Vectors ORI_SV40 (RRID: Addgene_99309) and ORI_neg.cont (RRID: Addgene_99315) were used as positive and negative controls.

Article Title: Dynamic HSF2 regulation drives breast cancer progression by steering the balance between proliferation and invasion
Article Snippet: Following two weeks of culturing, the negative lentiviral status was confirmed for each cell line using the HIV-1 p24 DuoSet ELISA rom kit (DY7360-05, R&D Systems). .. The plasmids used for the luciferase assay were generated by cloning 1 kb of either the human HSF2 promoter or MMP9 promoter upstream of the respective TSS into a STARR-seq luciferase validation vector_ORI_empty vector (#99297, Addgene). ..

Generated:

Article Title: Dynamic HSF2 regulation drives breast cancer progression by steering the balance between proliferation and invasion
Article Snippet: Following two weeks of culturing, the negative lentiviral status was confirmed for each cell line using the HIV-1 p24 DuoSet ELISA rom kit (DY7360-05, R&D Systems). .. The plasmids used for the luciferase assay were generated by cloning 1 kb of either the human HSF2 promoter or MMP9 promoter upstream of the respective TSS into a STARR-seq luciferase validation vector_ORI_empty vector (#99297, Addgene). ..



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Novel motifs affect gene transcription in Jurkats. A Shown, is a diagram of <t>the</t> <t>STARR-seq</t> oligo library design. The figure was adapted from Georgakopoulos-Soares et al under the Creative Commons license http://creativecommons.org/licenses/by/4.0/ . Changes were made to the figure to account for the differences in our overall library design. Eighteen candidate motifs (nine novel and nine TFBS motifs) were embedded in a synthetic background DNA sequence. Each sequence contained one to three instances of a motif, separated by 10bp. The oligonucleotide library contains every possible combination, position, and orientation of the 18 candidate motifs. B The mean activity score for the 18 motifs in their respective orientations for Jurkat and ( C ) K562 cells are shown above. Mean activity scores were obtained from oligos containing the motif of interest only in its indicated orientation. Motifs with a significant effect on gene transcription were identified using a two-sided t-test that compared oligos containing the motif of interest to those that do not contain the motif. Only oligos containing 1-3 instances of the given motif in its respective orientation were used. Motifs with a significant effect of gene transcription are indicated as solid bars (Bonferroni corrected, p -value < 0.001, |Cohen's D| > 0.5). Error bars represent the standard error of activity scores. D Linear modelling was used to determine if there was an association between the number of copies of a motif and the mean activity score for the motifs with a significant effect on gene transcription in Jurkat cells and ( E ) K562 cells (Bonferroni corrected, p -value < 0.007). Only oligos containing one to three copies of the motif of interest were included in the analysis
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Novel motifs affect gene transcription in Jurkats. A Shown, is a diagram of <t>the</t> <t>STARR-seq</t> oligo library design. The figure was adapted from Georgakopoulos-Soares et al under the Creative Commons license http://creativecommons.org/licenses/by/4.0/ . Changes were made to the figure to account for the differences in our overall library design. Eighteen candidate motifs (nine novel and nine TFBS motifs) were embedded in a synthetic background DNA sequence. Each sequence contained one to three instances of a motif, separated by 10bp. The oligonucleotide library contains every possible combination, position, and orientation of the 18 candidate motifs. B The mean activity score for the 18 motifs in their respective orientations for Jurkat and ( C ) K562 cells are shown above. Mean activity scores were obtained from oligos containing the motif of interest only in its indicated orientation. Motifs with a significant effect on gene transcription were identified using a two-sided t-test that compared oligos containing the motif of interest to those that do not contain the motif. Only oligos containing 1-3 instances of the given motif in its respective orientation were used. Motifs with a significant effect of gene transcription are indicated as solid bars (Bonferroni corrected, p -value < 0.001, |Cohen's D| > 0.5). Error bars represent the standard error of activity scores. D Linear modelling was used to determine if there was an association between the number of copies of a motif and the mean activity score for the motifs with a significant effect on gene transcription in Jurkat cells and ( E ) K562 cells (Bonferroni corrected, p -value < 0.007). Only oligos containing one to three copies of the motif of interest were included in the analysis
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Novel motifs affect gene transcription in Jurkats. A Shown, is a diagram of <t>the</t> <t>STARR-seq</t> oligo library design. The figure was adapted from Georgakopoulos-Soares et al under the Creative Commons license http://creativecommons.org/licenses/by/4.0/ . Changes were made to the figure to account for the differences in our overall library design. Eighteen candidate motifs (nine novel and nine TFBS motifs) were embedded in a synthetic background DNA sequence. Each sequence contained one to three instances of a motif, separated by 10bp. The oligonucleotide library contains every possible combination, position, and orientation of the 18 candidate motifs. B The mean activity score for the 18 motifs in their respective orientations for Jurkat and ( C ) K562 cells are shown above. Mean activity scores were obtained from oligos containing the motif of interest only in its indicated orientation. Motifs with a significant effect on gene transcription were identified using a two-sided t-test that compared oligos containing the motif of interest to those that do not contain the motif. Only oligos containing 1-3 instances of the given motif in its respective orientation were used. Motifs with a significant effect of gene transcription are indicated as solid bars (Bonferroni corrected, p -value < 0.001, |Cohen's D| > 0.5). Error bars represent the standard error of activity scores. D Linear modelling was used to determine if there was an association between the number of copies of a motif and the mean activity score for the motifs with a significant effect on gene transcription in Jurkat cells and ( E ) K562 cells (Bonferroni corrected, p -value < 0.007). Only oligos containing one to three copies of the motif of interest were included in the analysis
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Novel motifs affect gene transcription in Jurkats. A Shown, is a diagram of the STARR-seq oligo library design. The figure was adapted from Georgakopoulos-Soares et al under the Creative Commons license http://creativecommons.org/licenses/by/4.0/ . Changes were made to the figure to account for the differences in our overall library design. Eighteen candidate motifs (nine novel and nine TFBS motifs) were embedded in a synthetic background DNA sequence. Each sequence contained one to three instances of a motif, separated by 10bp. The oligonucleotide library contains every possible combination, position, and orientation of the 18 candidate motifs. B The mean activity score for the 18 motifs in their respective orientations for Jurkat and ( C ) K562 cells are shown above. Mean activity scores were obtained from oligos containing the motif of interest only in its indicated orientation. Motifs with a significant effect on gene transcription were identified using a two-sided t-test that compared oligos containing the motif of interest to those that do not contain the motif. Only oligos containing 1-3 instances of the given motif in its respective orientation were used. Motifs with a significant effect of gene transcription are indicated as solid bars (Bonferroni corrected, p -value < 0.001, |Cohen's D| > 0.5). Error bars represent the standard error of activity scores. D Linear modelling was used to determine if there was an association between the number of copies of a motif and the mean activity score for the motifs with a significant effect on gene transcription in Jurkat cells and ( E ) K562 cells (Bonferroni corrected, p -value < 0.007). Only oligos containing one to three copies of the motif of interest were included in the analysis

Journal: BMC Genomics

Article Title: Identification of novel DNA sequence motifs that modulate transcription in T cells

doi: 10.1186/s12864-025-12425-9

Figure Lengend Snippet: Novel motifs affect gene transcription in Jurkats. A Shown, is a diagram of the STARR-seq oligo library design. The figure was adapted from Georgakopoulos-Soares et al under the Creative Commons license http://creativecommons.org/licenses/by/4.0/ . Changes were made to the figure to account for the differences in our overall library design. Eighteen candidate motifs (nine novel and nine TFBS motifs) were embedded in a synthetic background DNA sequence. Each sequence contained one to three instances of a motif, separated by 10bp. The oligonucleotide library contains every possible combination, position, and orientation of the 18 candidate motifs. B The mean activity score for the 18 motifs in their respective orientations for Jurkat and ( C ) K562 cells are shown above. Mean activity scores were obtained from oligos containing the motif of interest only in its indicated orientation. Motifs with a significant effect on gene transcription were identified using a two-sided t-test that compared oligos containing the motif of interest to those that do not contain the motif. Only oligos containing 1-3 instances of the given motif in its respective orientation were used. Motifs with a significant effect of gene transcription are indicated as solid bars (Bonferroni corrected, p -value < 0.001, |Cohen's D| > 0.5). Error bars represent the standard error of activity scores. D Linear modelling was used to determine if there was an association between the number of copies of a motif and the mean activity score for the motifs with a significant effect on gene transcription in Jurkat cells and ( E ) K562 cells (Bonferroni corrected, p -value < 0.007). Only oligos containing one to three copies of the motif of interest were included in the analysis

Article Snippet: After designing the library, the oligonucleotide sequences were flanked by AgeI and SalI restriction sites to facilitate cloning into the STARR-seq vector (hSTARR-seq_ORI, Addgene #99296) and the necessary priming and Illumina adapter sequences were added to enable sequencing (Supplemental Table S3).

Techniques: Sequencing, Activity Assay