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anti cstf64  (Bethyl)


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    Structured Review

    Bethyl anti cstf64
    Anti Cstf64, supplied by Bethyl, used in various techniques. Bioz Stars score: 93/100, based on 40 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+cstf64/CSTF64+Antibody/pm39798570-418-46-47
    Average 93 stars, based on 40 article reviews
    anti cstf64 - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    other:

    Article Title: tRIP‐seq reveals repression of premature polyadenylation by co‐transcriptional FUS‐U1 snRNP assembly
    Article Snippet: Anti‐RBFOX2 (A300‐864A), anti‐CstF64 (A301‐092A), and anti‐CFIm59 (A301‐359A) were purchased from Bethyl Laboratories.

    Article Title: Human TREX component Thoc5 affects alternative polyadenylation site choice by recruiting mammalian cleavage factor I.
    Article Snippet: Anti-SR (16H3, Zymed) (42), antiCPSF68 (CFIm68), anti-CPSF73, anti-CstF64, antiCstF77, anti-hFip1 (Bethyl Laboratories), anti-mouse IgG (Zymed or Rockland), anti-CPSF100 (Sigma), anti-b-actin (AC-15, Sigma), anti-Thoc6 (Abnova), anti-Aly (11G5, Abcam) and normal mouse IgG (Santa Cruz) antibodies were commercially acquired.


    Article Title: Human TREX component Thoc5 affects alternative polyadenylation site choice by recruiting mammalian cleavage factor I
    Article Snippet: Anti-SR (16H3, Zymed) , anti-CPSF68 (CFIm68), anti-CPSF73, anti-CstF64, anti-CstF77, anti-hFip1 (Bethyl Laboratories), anti-mouse IgG (Zymed or Rockland), anti-CPSF100 (Sigma), anti-β-actin (AC-15, Sigma), anti-Thoc6 (Abnova), anti-Aly (11G5, Abcam) and normal mouse IgG (Santa Cruz) antibodies were commercially acquired.

    Article Title: RBBP6 isoforms regulate the human polyadenylation machinery and modulate expression of mRNAs with AU-rich 3′ UTRs
    Article Snippet: Anti-CPSF100 and anti-CstF64 ( ) were made in our laboratory, and all other antibodies for 3′ processing factors were from Bethyl Laboratories.

    Article Title: A Cancer-Specific Ubiquitin Ligase Drives mRNA Alternative Polyadenylation by Ubiquitinating the mRNA 3' End Processing Complex.
    Article Snippet: Commercial antibodies used: anti-PCF11 (Bethyl Laboratories, A303-706A), anti-RNAP II (Cell Signaling Technology, 14958S), anti-CLP1 (Abcam, ab133669), anti-HUWE1 (Novus Biologicals, NB100-652), anti-GAPDH (Cell Signaling Technology, 2118S), anti-FLAG (Sigma, F3165), anti-Myc (Roche, 11666606001), anti-Actin (Abcam, ab6276), anti-Tubulin (Sigma, T5168), antiCCND1 (ABclonal, A11022), anti-CCND2 (ABclonal, A1773), anti-CCND3 (ABclonal, A0746), anti-phospho-Rb S807/811 (Cell Signaling Technology, 9308T), anti-Rb (Cell Signaling Technology, 9309T), anti-PTEN (Bethyl Laboratories, A300-701A), anti-phospho-Akt T308 (Cell Signaling Technology, 4056S), anti-Akt (Cell Signaling Technology, 4691S), anti-CPSF160 (Bethyl Laboratories, A301-580A), anti-CPSF100 (Bethyl Laboratories, A301-581A), anti-CPSF73 (Bethyl Laboratories, A301-091A), anti-CstF64 (Bethyl Laboratories, A301-092A), anti-TauCstF64 (Bethyl Laboratories, A301-487A), anti-CFIm68 (Bethyl Laboratories, A301-356A), antiCFIm59 (Bethyl Laboratories, A301-359A), anti-CFIm25 (Proteintech, 66335-1-Ig), anti-XRN2 (Bethyl Laboratories, A301-103A), Donkey anti-Rabbit IgG (GE, NA934V), and Sheep anti-Mouse IgG (GE, NA931V).

    Chromatin Immunoprecipitation:

    Article Title: Human snRNA genes use polyadenylation factors to promote efficient transcription termination
    Article Snippet: .. Antibodies used in ChIP experiments were purchased from the following manufacturers: anti-pol II (Sigma, N-20), anti H3 (abcam, ab1791), anti-NELF-A (Santa Cruz, sc-32911), anti-Pcf11 (Bethyl, A303-706A), anti-Ssu72 (Santa Cruz, N-16) and anti-Cstf64 (Bethyl, A301-092A). ..



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    Effect of U1 AMO on the recruitment of core intronic PAS processing factors onto chromatin and pre-mRNA. A , in vitro cleavage/polyadenylation and in vitro cleavage assays using HeLa NE and RNA substrates derived from intronic PAS of nr3c1 gene. Three repeats of MS2 sequences were added to the 5′ end of the PAS RNA to facilitate the process of protein purification. As negative control, a mutant PAS RNA harboring a point mutation in the core hexamer AAUAAA was prepared simultaneously. The PAS RNA sequences are listed in <xref ref-type=Table S4 . The polyadenylated or cleaved RNA products are indicated with red arrows . B , silver staining of protein complexes purified from HeLa NE using the indicated PAS RNAs. Potential intronic PAS processing factors, which are indicated with red arrows , could be purified by wt but not m1 PAS RNAs. C , validation of mass spectrometric results by Western blotting analysis using antibodies against indicated proteins. The input is 2% of the total lysates. D , metagene plots of CPSF160, WDR33, and CSTF77 chromatin immunoprecipitation (ChIP-Seq) reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. E , metagene plots of WDR33 and CSTF64 iCLIP-Seq reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). For intronic PCPAed genes, a second metagene plot was made for each ChIP-Seq/iCLIP-Seq by replacing the default TES (transcription end site) with intronic PCPA sites. Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. F , a schematic diagram summarizing the key finding in our study. The details are described in the main body of the text. iCLIP-Seq, individual-nucleotide resolution CrossLinking and ImmunoPrecipitation sequencing; PCPA, premature cleavage and polyadenylation. " width="250" height="auto" />
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    Effect of U1 AMO on the recruitment of core intronic PAS processing factors onto chromatin and pre-mRNA. A , in vitro cleavage/polyadenylation and in vitro cleavage assays using HeLa NE and RNA substrates derived from intronic PAS of nr3c1 gene. Three repeats of MS2 sequences were added to the 5′ end of the PAS RNA to facilitate the process of protein purification. As negative control, a mutant PAS RNA harboring a point mutation in the core hexamer AAUAAA was prepared simultaneously. The PAS RNA sequences are listed in <xref ref-type=Table S4 . The polyadenylated or cleaved RNA products are indicated with red arrows . B , silver staining of protein complexes purified from HeLa NE using the indicated PAS RNAs. Potential intronic PAS processing factors, which are indicated with red arrows , could be purified by wt but not m1 PAS RNAs. C , validation of mass spectrometric results by Western blotting analysis using antibodies against indicated proteins. The input is 2% of the total lysates. D , metagene plots of CPSF160, WDR33, and CSTF77 chromatin immunoprecipitation (ChIP-Seq) reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. E , metagene plots of WDR33 and CSTF64 iCLIP-Seq reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). For intronic PCPAed genes, a second metagene plot was made for each ChIP-Seq/iCLIP-Seq by replacing the default TES (transcription end site) with intronic PCPA sites. Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. F , a schematic diagram summarizing the key finding in our study. The details are described in the main body of the text. iCLIP-Seq, individual-nucleotide resolution CrossLinking and ImmunoPrecipitation sequencing; PCPA, premature cleavage and polyadenylation. " width="250" height="auto" />
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    Image Search Results


    Effect of U1 AMO on the recruitment of core intronic PAS processing factors onto chromatin and pre-mRNA. A , in vitro cleavage/polyadenylation and in vitro cleavage assays using HeLa NE and RNA substrates derived from intronic PAS of nr3c1 gene. Three repeats of MS2 sequences were added to the 5′ end of the PAS RNA to facilitate the process of protein purification. As negative control, a mutant PAS RNA harboring a point mutation in the core hexamer AAUAAA was prepared simultaneously. The PAS RNA sequences are listed in <xref ref-type=Table S4 . The polyadenylated or cleaved RNA products are indicated with red arrows . B , silver staining of protein complexes purified from HeLa NE using the indicated PAS RNAs. Potential intronic PAS processing factors, which are indicated with red arrows , could be purified by wt but not m1 PAS RNAs. C , validation of mass spectrometric results by Western blotting analysis using antibodies against indicated proteins. The input is 2% of the total lysates. D , metagene plots of CPSF160, WDR33, and CSTF77 chromatin immunoprecipitation (ChIP-Seq) reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. E , metagene plots of WDR33 and CSTF64 iCLIP-Seq reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). For intronic PCPAed genes, a second metagene plot was made for each ChIP-Seq/iCLIP-Seq by replacing the default TES (transcription end site) with intronic PCPA sites. Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. F , a schematic diagram summarizing the key finding in our study. The details are described in the main body of the text. iCLIP-Seq, individual-nucleotide resolution CrossLinking and ImmunoPrecipitation sequencing; PCPA, premature cleavage and polyadenylation. " width="100%" height="100%">

    Journal: The Journal of Biological Chemistry

    Article Title: The U1 antisense morpholino oligonucleotide (AMO) disrupts U1 snRNP structure to promote intronic PCPA modification of pre-mRNAs

    doi: 10.1016/j.jbc.2023.104854

    Figure Lengend Snippet: Effect of U1 AMO on the recruitment of core intronic PAS processing factors onto chromatin and pre-mRNA. A , in vitro cleavage/polyadenylation and in vitro cleavage assays using HeLa NE and RNA substrates derived from intronic PAS of nr3c1 gene. Three repeats of MS2 sequences were added to the 5′ end of the PAS RNA to facilitate the process of protein purification. As negative control, a mutant PAS RNA harboring a point mutation in the core hexamer AAUAAA was prepared simultaneously. The PAS RNA sequences are listed in Table S4 . The polyadenylated or cleaved RNA products are indicated with red arrows . B , silver staining of protein complexes purified from HeLa NE using the indicated PAS RNAs. Potential intronic PAS processing factors, which are indicated with red arrows , could be purified by wt but not m1 PAS RNAs. C , validation of mass spectrometric results by Western blotting analysis using antibodies against indicated proteins. The input is 2% of the total lysates. D , metagene plots of CPSF160, WDR33, and CSTF77 chromatin immunoprecipitation (ChIP-Seq) reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. E , metagene plots of WDR33 and CSTF64 iCLIP-Seq reads in control and U1 AMO–treated HeLa cells for all actively expressed genes (n = 13,217), intronic PCPAed genes (n = 5937), and other nonintronic PCPAed genes (n = 7280). For intronic PCPAed genes, a second metagene plot was made for each ChIP-Seq/iCLIP-Seq by replacing the default TES (transcription end site) with intronic PCPA sites. Control represents control AMO–treated HeLa cells, and U1 represents U1 AMO–treated HeLa cells. F , a schematic diagram summarizing the key finding in our study. The details are described in the main body of the text. iCLIP-Seq, individual-nucleotide resolution CrossLinking and ImmunoPrecipitation sequencing; PCPA, premature cleavage and polyadenylation.

    Article Snippet: The primary antibodies (WDR33 [A301–152A] and CstF64 [A301–092A]) were purchased from Bethyl.

    Techniques: In Vitro, Derivative Assay, Protein Purification, Negative Control, Mutagenesis, Silver Staining, Purification, Biomarker Discovery, Western Blot, Chromatin Immunoprecipitation, ChIP-sequencing, Control, Immunoprecipitation, Sequencing