Review



psip1 novus  (Santa Cruz Biotechnology)


Bioz Verified Symbol Santa Cruz Biotechnology is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 92

    Structured Review

    Santa Cruz Biotechnology psip1 novus
    Isoform switch from PBX1a and PBX1b during hESC differentiation. a Genome browser view shows the AS event and H3K36me3 signals of PBX1 upon hESC differentiation. The green horizontal bars below the ChIP-seq tracks indicate the narrow peaks called by MACS2. b The inclusion level for exon 7 of PBX1 is significantly correlated to the H3K36me3 signals over this exon across cell lineages. c The sequence difference of three protein isoforms of PBX1 and the main functional domains. d The relative expressions of PBX1a and PBX1b in 56 cells/tissues, representing the differential expressions of two isoforms in three groups based on their developmental states. e The expression levels of NANOG and OCT4 genes are negatively correlated with the expression of PBX1b. f The expression levels of <t>PSIP1</t> and SRSF1 show significant positive correlations with the expression level of PBX1a. Also see Additional file : Figures S9, S10
    Psip1 Novus, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/psip1+novus/PSIP1+Antibody/pmc06138936-395-19-23
    Average 92 stars, based on 8 article reviews
    psip1 novus - by Bioz Stars, 2026-09
    92/100 stars

    Images

    1) Product Images from "Alternative splicing links histone modifications to stem cell fate decision"

    Article Title: Alternative splicing links histone modifications to stem cell fate decision

    Journal: Genome Biology

    doi: 10.1186/s13059-018-1512-3

    Isoform switch from PBX1a and PBX1b during hESC differentiation. a Genome browser view shows the AS event and H3K36me3 signals of PBX1 upon hESC differentiation. The green horizontal bars below the ChIP-seq tracks indicate the narrow peaks called by MACS2. b The inclusion level for exon 7 of PBX1 is significantly correlated to the H3K36me3 signals over this exon across cell lineages. c The sequence difference of three protein isoforms of PBX1 and the main functional domains. d The relative expressions of PBX1a and PBX1b in 56 cells/tissues, representing the differential expressions of two isoforms in three groups based on their developmental states. e The expression levels of NANOG and OCT4 genes are negatively correlated with the expression of PBX1b. f The expression levels of PSIP1 and SRSF1 show significant positive correlations with the expression level of PBX1a. Also see Additional file : Figures S9, S10
    Figure Legend Snippet: Isoform switch from PBX1a and PBX1b during hESC differentiation. a Genome browser view shows the AS event and H3K36me3 signals of PBX1 upon hESC differentiation. The green horizontal bars below the ChIP-seq tracks indicate the narrow peaks called by MACS2. b The inclusion level for exon 7 of PBX1 is significantly correlated to the H3K36me3 signals over this exon across cell lineages. c The sequence difference of three protein isoforms of PBX1 and the main functional domains. d The relative expressions of PBX1a and PBX1b in 56 cells/tissues, representing the differential expressions of two isoforms in three groups based on their developmental states. e The expression levels of NANOG and OCT4 genes are negatively correlated with the expression of PBX1b. f The expression levels of PSIP1 and SRSF1 show significant positive correlations with the expression level of PBX1a. Also see Additional file : Figures S9, S10

    Techniques Used: ChIP-sequencing, Sequencing, Functional Assay, Expressing

    Isoform switch of PBX1 links H3K36me3 to hESC fate decision. a qRT-PCR and western blot show the expression levels of Yamanaka factors in H1, MSC, and IMR90 cells. Whiskers denote the standard deviations of three replicates. b RT-PCR and western blot show the isoform switches between PBX1a and PBX1b from H1 cells to differentiated cells. c i. ChIP-PCR shows the differential binding of PBX1b to NANOG promoter in H1 cells and differentiated cells; ii. ChIP-PCR shows the reduced H3K36me3 signal in differentiated cells; iii. ChIP-PCR shows the differential recruitment of PSIP1 to exon 7 of PBX1. d RIP-PCR show the differential recruitment of SRSF1 around exon 7 of PBX1. e Co-IP shows the overall physical interaction between PSIP1 and SRSF1 in all studied cell types. f The mechanism by which H3K36me3 is linked to cell fate decision by regulating the isoform switch of PBX1, which functions upstream of the pluripotency regulatory network. Also see Additional file : Figures S9, S10
    Figure Legend Snippet: Isoform switch of PBX1 links H3K36me3 to hESC fate decision. a qRT-PCR and western blot show the expression levels of Yamanaka factors in H1, MSC, and IMR90 cells. Whiskers denote the standard deviations of three replicates. b RT-PCR and western blot show the isoform switches between PBX1a and PBX1b from H1 cells to differentiated cells. c i. ChIP-PCR shows the differential binding of PBX1b to NANOG promoter in H1 cells and differentiated cells; ii. ChIP-PCR shows the reduced H3K36me3 signal in differentiated cells; iii. ChIP-PCR shows the differential recruitment of PSIP1 to exon 7 of PBX1. d RIP-PCR show the differential recruitment of SRSF1 around exon 7 of PBX1. e Co-IP shows the overall physical interaction between PSIP1 and SRSF1 in all studied cell types. f The mechanism by which H3K36me3 is linked to cell fate decision by regulating the isoform switch of PBX1, which functions upstream of the pluripotency regulatory network. Also see Additional file : Figures S9, S10

    Techniques Used: Quantitative RT-PCR, Western Blot, Expressing, Reverse Transcription Polymerase Chain Reaction, Binding Assay, Co-Immunoprecipitation Assay

    Related Articles

    Chromatin Immunoprecipitation:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Magnetic Beads:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    ChIP-sequencing:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Sequencing:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Functional Assay:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Expressing:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Quantitative RT-PCR:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Western Blot:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Reverse Transcription Polymerase Chain Reaction:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Binding Assay:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Co-Immunoprecipitation Assay:

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Article Title: Alternative splicing links histone modifications to stem cell fate decision
    Article Snippet: The protein-DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).



    Similar Products

    92
    Santa Cruz Biotechnology psip1 novus
    Isoform switch from PBX1a and PBX1b during hESC differentiation. a Genome browser view shows the AS event and H3K36me3 signals of PBX1 upon hESC differentiation. The green horizontal bars below the ChIP-seq tracks indicate the narrow peaks called by MACS2. b The inclusion level for exon 7 of PBX1 is significantly correlated to the H3K36me3 signals over this exon across cell lineages. c The sequence difference of three protein isoforms of PBX1 and the main functional domains. d The relative expressions of PBX1a and PBX1b in 56 cells/tissues, representing the differential expressions of two isoforms in three groups based on their developmental states. e The expression levels of NANOG and OCT4 genes are negatively correlated with the expression of PBX1b. f The expression levels of <t>PSIP1</t> and SRSF1 show significant positive correlations with the expression level of PBX1a. Also see Additional file : Figures S9, S10
    Psip1 Novus, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/psip1+novus/PSIP1+Antibody/pmc06138936-395-19-23
    Average 92 stars, based on 1 article reviews
    psip1 novus - by Bioz Stars, 2026-09
    92/100 stars
      Buy from Supplier

    Image Search Results


    Isoform switch from PBX1a and PBX1b during hESC differentiation. a Genome browser view shows the AS event and H3K36me3 signals of PBX1 upon hESC differentiation. The green horizontal bars below the ChIP-seq tracks indicate the narrow peaks called by MACS2. b The inclusion level for exon 7 of PBX1 is significantly correlated to the H3K36me3 signals over this exon across cell lineages. c The sequence difference of three protein isoforms of PBX1 and the main functional domains. d The relative expressions of PBX1a and PBX1b in 56 cells/tissues, representing the differential expressions of two isoforms in three groups based on their developmental states. e The expression levels of NANOG and OCT4 genes are negatively correlated with the expression of PBX1b. f The expression levels of PSIP1 and SRSF1 show significant positive correlations with the expression level of PBX1a. Also see Additional file : Figures S9, S10

    Journal: Genome Biology

    Article Title: Alternative splicing links histone modifications to stem cell fate decision

    doi: 10.1186/s13059-018-1512-3

    Figure Lengend Snippet: Isoform switch from PBX1a and PBX1b during hESC differentiation. a Genome browser view shows the AS event and H3K36me3 signals of PBX1 upon hESC differentiation. The green horizontal bars below the ChIP-seq tracks indicate the narrow peaks called by MACS2. b The inclusion level for exon 7 of PBX1 is significantly correlated to the H3K36me3 signals over this exon across cell lineages. c The sequence difference of three protein isoforms of PBX1 and the main functional domains. d The relative expressions of PBX1a and PBX1b in 56 cells/tissues, representing the differential expressions of two isoforms in three groups based on their developmental states. e The expression levels of NANOG and OCT4 genes are negatively correlated with the expression of PBX1b. f The expression levels of PSIP1 and SRSF1 show significant positive correlations with the expression level of PBX1a. Also see Additional file : Figures S9, S10

    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Techniques: ChIP-sequencing, Sequencing, Functional Assay, Expressing

    Isoform switch of PBX1 links H3K36me3 to hESC fate decision. a qRT-PCR and western blot show the expression levels of Yamanaka factors in H1, MSC, and IMR90 cells. Whiskers denote the standard deviations of three replicates. b RT-PCR and western blot show the isoform switches between PBX1a and PBX1b from H1 cells to differentiated cells. c i. ChIP-PCR shows the differential binding of PBX1b to NANOG promoter in H1 cells and differentiated cells; ii. ChIP-PCR shows the reduced H3K36me3 signal in differentiated cells; iii. ChIP-PCR shows the differential recruitment of PSIP1 to exon 7 of PBX1. d RIP-PCR show the differential recruitment of SRSF1 around exon 7 of PBX1. e Co-IP shows the overall physical interaction between PSIP1 and SRSF1 in all studied cell types. f The mechanism by which H3K36me3 is linked to cell fate decision by regulating the isoform switch of PBX1, which functions upstream of the pluripotency regulatory network. Also see Additional file : Figures S9, S10

    Journal: Genome Biology

    Article Title: Alternative splicing links histone modifications to stem cell fate decision

    doi: 10.1186/s13059-018-1512-3

    Figure Lengend Snippet: Isoform switch of PBX1 links H3K36me3 to hESC fate decision. a qRT-PCR and western blot show the expression levels of Yamanaka factors in H1, MSC, and IMR90 cells. Whiskers denote the standard deviations of three replicates. b RT-PCR and western blot show the isoform switches between PBX1a and PBX1b from H1 cells to differentiated cells. c i. ChIP-PCR shows the differential binding of PBX1b to NANOG promoter in H1 cells and differentiated cells; ii. ChIP-PCR shows the reduced H3K36me3 signal in differentiated cells; iii. ChIP-PCR shows the differential recruitment of PSIP1 to exon 7 of PBX1. d RIP-PCR show the differential recruitment of SRSF1 around exon 7 of PBX1. e Co-IP shows the overall physical interaction between PSIP1 and SRSF1 in all studied cell types. f The mechanism by which H3K36me3 is linked to cell fate decision by regulating the isoform switch of PBX1, which functions upstream of the pluripotency regulatory network. Also see Additional file : Figures S9, S10

    Article Snippet: The protein–DNA complex was precipitated with ChIP-Grade Protein G Magnetic Beads (Cell Signalling) and ChIP-validated antibodies against H3K36me3 (Abcam), PSIP1 (Novus), and PBX1b (Santa Cruz).

    Techniques: Quantitative RT-PCR, Western Blot, Expressing, Reverse Transcription Polymerase Chain Reaction, Binding Assay, Co-Immunoprecipitation Assay