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rbfox1 transgenic mice human rbfox1 cdna  (Addgene inc)


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    Structured Review

    Addgene inc rbfox1 transgenic mice human rbfox1 cdna
    Rbfox1 Transgenic Mice Human Rbfox1 Cdna, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+rbfox1+cdna/pENTR-A2BP1+(Plasmid+%2316176)/pm41928095-78-2-10
    Average 93 stars, based on 6 article reviews
    rbfox1 transgenic mice human rbfox1 cdna - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Clone Assay:

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology
    Article Snippet: .. Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004). ..

    Plasmid Preparation:

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology
    Article Snippet: .. Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004). ..

    Sequencing:

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology
    Article Snippet: .. Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004). ..



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    93
    Addgene inc rbfox1 transgenic mice human rbfox1 cdna
    Rbfox1 Transgenic Mice Human Rbfox1 Cdna, supplied by Addgene inc, 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/product/human+rbfox1+cdna/pENTR-A2BP1+(Plasmid+%2316176)/pm41928095-78-2-10
    Average 93 stars, based on 1 article reviews
    rbfox1 transgenic mice human rbfox1 cdna - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    93
    Addgene inc human rbfox1 cdna
    ( A ) Normalized counts of the three RBFOX genes in striatal RNA from 3.5 month-old WT (n=3) and R6/1 mice (n=3) according to RNA-seq datasets in Elorza et al . 15 ( B ) Quantification of <t>Rbfox1</t> transcript levels by RT-qPCR in striatal RNA from 3.5 month-old WT (n=7) and R6/1 mice (n=7) (Student’s t-test; * P < 0.05). ( C ) Rbfox1 immunohistochemistry in striatum of 3.5 month-old WT and R6/1 mice. ( E ) Representative RBFOX1 immunohistochemistry staining in striatum of control and HD subjects.
    Human Rbfox1 Cdna, supplied by Addgene inc, 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/product/human+rbfox1+cdna/pENTR-A2BP1+(Plasmid+%2316176)/bio_rxiv__2024__11__06__622223-111-0-5
    Average 93 stars, based on 1 article reviews
    human rbfox1 cdna - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    Image Search Results


    ( A ) Normalized counts of the three RBFOX genes in striatal RNA from 3.5 month-old WT (n=3) and R6/1 mice (n=3) according to RNA-seq datasets in Elorza et al . 15 ( B ) Quantification of Rbfox1 transcript levels by RT-qPCR in striatal RNA from 3.5 month-old WT (n=7) and R6/1 mice (n=7) (Student’s t-test; * P < 0.05). ( C ) Rbfox1 immunohistochemistry in striatum of 3.5 month-old WT and R6/1 mice. ( E ) Representative RBFOX1 immunohistochemistry staining in striatum of control and HD subjects.

    Journal: bioRxiv

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology

    doi: 10.1101/2024.11.06.622223

    Figure Lengend Snippet: ( A ) Normalized counts of the three RBFOX genes in striatal RNA from 3.5 month-old WT (n=3) and R6/1 mice (n=3) according to RNA-seq datasets in Elorza et al . 15 ( B ) Quantification of Rbfox1 transcript levels by RT-qPCR in striatal RNA from 3.5 month-old WT (n=7) and R6/1 mice (n=7) (Student’s t-test; * P < 0.05). ( C ) Rbfox1 immunohistochemistry in striatum of 3.5 month-old WT and R6/1 mice. ( E ) Representative RBFOX1 immunohistochemistry staining in striatum of control and HD subjects.

    Article Snippet: Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004).

    Techniques: RNA Sequencing, Quantitative RT-PCR, Immunohistochemistry, Staining, Control

    ( A ) Mice expressing tTA under control of the CamKII promoter (CamKII-tTA mice) were bred with mice carrying the β-Gal-BiTetO-RBFOX1 or β-Gal-BiTetO-U2AF2 construct to yield TgRBFOX1 (CamKII-tTA:β-Gal-BiTetO-RBFOX1) mice or TgU2AF2 (CamKII-tTA:β-Gal-BiTetO-U2AF2) . ( B ) Immunohistochemistry with anti-RBFOX1 or anti-U2AF2 antibody in sagittal sections from 1.5 month-old WT, TgRBFOX1 or TgU2AF2 mice.

    Journal: bioRxiv

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology

    doi: 10.1101/2024.11.06.622223

    Figure Lengend Snippet: ( A ) Mice expressing tTA under control of the CamKII promoter (CamKII-tTA mice) were bred with mice carrying the β-Gal-BiTetO-RBFOX1 or β-Gal-BiTetO-U2AF2 construct to yield TgRBFOX1 (CamKII-tTA:β-Gal-BiTetO-RBFOX1) mice or TgU2AF2 (CamKII-tTA:β-Gal-BiTetO-U2AF2) . ( B ) Immunohistochemistry with anti-RBFOX1 or anti-U2AF2 antibody in sagittal sections from 1.5 month-old WT, TgRBFOX1 or TgU2AF2 mice.

    Article Snippet: Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004).

    Techniques: Expressing, Control, Construct, Immunohistochemistry

    (A) Gel shows RT-PCR amplification of Tg-RBFOX1 or TgU2AF2 mRNA in wild-type, MildTgRBFOX1 or MildTgU2AF2 and StrongTgRBFOX1 or StrongTgU2AF2 mice. (B) Histogram shows brain weight of WT (n=5/n=8), MildTgRBFOX1 (n=7) or MildTgU2AF2 (n=5) and Strong TgRBFOX1 (n=7) or Strong TgU2AF2 (n=6) mice (ANOVA, followed by Tukey’s post hoc test; *P < 0.05;**P < 0.01; ***P < 0.001).

    Journal: bioRxiv

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology

    doi: 10.1101/2024.11.06.622223

    Figure Lengend Snippet: (A) Gel shows RT-PCR amplification of Tg-RBFOX1 or TgU2AF2 mRNA in wild-type, MildTgRBFOX1 or MildTgU2AF2 and StrongTgRBFOX1 or StrongTgU2AF2 mice. (B) Histogram shows brain weight of WT (n=5/n=8), MildTgRBFOX1 (n=7) or MildTgU2AF2 (n=5) and Strong TgRBFOX1 (n=7) or Strong TgU2AF2 (n=6) mice (ANOVA, followed by Tukey’s post hoc test; *P < 0.05;**P < 0.01; ***P < 0.001).

    Article Snippet: Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004).

    Techniques: Reverse Transcription Polymerase Chain Reaction, Amplification

    ( A ) Venn diagram showing the 83 genes in the intersection between the 245 genes with exons mis-spliced in Huntington’s disease 15 and the 543 genes with RBFOX-direct target exons 25 ( B ) Venn diagram showing the 76 genes in the intersection between the 245 genes with exons mis-spliced in Huntington’s disease 15 and the 966 genes that are functional targets of Rbfox1 according to Supplementary Table 1. Representation factor (RF) was determined with Two-sided Fisher’s Exact test, using as background genes the human-mouse orthologous genes coincidentally detected in the human and mouse RNA-seq datasets used to define the Huntington’s disease mis-splicing signature 15 ( n = 12,882).

    Journal: bioRxiv

    Article Title: Correction of RBFOX1 deficit rescues Huntington’s disease mis-splicing and pathology

    doi: 10.1101/2024.11.06.622223

    Figure Lengend Snippet: ( A ) Venn diagram showing the 83 genes in the intersection between the 245 genes with exons mis-spliced in Huntington’s disease 15 and the 543 genes with RBFOX-direct target exons 25 ( B ) Venn diagram showing the 76 genes in the intersection between the 245 genes with exons mis-spliced in Huntington’s disease 15 and the 966 genes that are functional targets of Rbfox1 according to Supplementary Table 1. Representation factor (RF) was determined with Two-sided Fisher’s Exact test, using as background genes the human-mouse orthologous genes coincidentally detected in the human and mouse RNA-seq datasets used to define the Huntington’s disease mis-splicing signature 15 ( n = 12,882).

    Article Snippet: Human RBFOX1 cDNA (from pENTR-A2BP1, Addgene, 16176) or human U2AF2 cDNA (from pCDNA3-U2AF65-DYK, GenScript, OHu17874) were independently cloned into a plasmid containing a bidirectional TetO sequence that also harbors the β-galactosidase (β-Gal) reporter with a NLS (pBI-G, Clontech, 631004).

    Techniques: Functional Assay, RNA Sequencing