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ratio e2f4 proteintech group  (Proteintech)


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    Proteintech ratio e2f4 proteintech group
    Ratio E2f4 Proteintech Group, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+lin9/LIN9+Antibody/pmc11387118__Supplementary_Data2-4-6-8
    Average 93 stars, based on 9 article reviews
    ratio e2f4 proteintech group - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Bicinchoninic Acid Protein Assay:

    Article Title: Interactions between BRD4S, LOXL2, and MED1 drive cell cycle transcription in triple‐negative breast cancer
    Article Snippet: .. Nuclear extracts were quantified using Pierce BCA Protein Assay Kit (Thermo Scientific; #PIER23225) and 1 mg of nuclear extract was incubated overnight with a primary antibody, using: 2.5 μg anti‐BRD4 (Abcam; #ab128874), 5 μg anti‐MED1 (Bethyl Laboratories; A300‐793A), 4 μg anti‐Lin9 (Proteintech; #17882‐1‐AP), 4 μg anti‐B‐Myb (Proteintech; 18896‐1‐AP), or 4 μg anti‐FOXM1 (Proteintech; #13147‐1‐AP). .. The samples were then incubated with Protein A Dynabeads (Thermo Scientific; #10002D) for 1 h at 4°C.

    Incubation:

    Article Title: Interactions between BRD4S, LOXL2, and MED1 drive cell cycle transcription in triple‐negative breast cancer
    Article Snippet: .. Nuclear extracts were quantified using Pierce BCA Protein Assay Kit (Thermo Scientific; #PIER23225) and 1 mg of nuclear extract was incubated overnight with a primary antibody, using: 2.5 μg anti‐BRD4 (Abcam; #ab128874), 5 μg anti‐MED1 (Bethyl Laboratories; A300‐793A), 4 μg anti‐Lin9 (Proteintech; #17882‐1‐AP), 4 μg anti‐B‐Myb (Proteintech; 18896‐1‐AP), or 4 μg anti‐FOXM1 (Proteintech; #13147‐1‐AP). .. The samples were then incubated with Protein A Dynabeads (Thermo Scientific; #10002D) for 1 h at 4°C.



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    A. qRT-PCR of H1792 cells stably transduced with shCtrl (control) or shNFATc3 #2 (clone number) for NFATc3 and the DREAM target genes. B. CUT&RUN assays of A549 cells with anti-NFATc3 antibodies or IgG (control). The ACTB1 promoter served as a negative control. C. Promoter enrichment of transcription factors (TFs) on the DREAM target genes ( Kif22 and Ncapd2 ). Each dataset was visualized on the UCSC genome browser. The dataset accession numbers were shown. Red boxes indicate the co-enrichment of Lin9 and Nfat on the promoters. P values were calculated using Student’s t -test; error bars, standard deviation (SD).

    Journal: bioRxiv

    Article Title: NFATc3 Enhances DREAM Complex-Driven Transactivation

    doi: 10.64898/2026.01.12.699082

    Figure Lengend Snippet: A. qRT-PCR of H1792 cells stably transduced with shCtrl (control) or shNFATc3 #2 (clone number) for NFATc3 and the DREAM target genes. B. CUT&RUN assays of A549 cells with anti-NFATc3 antibodies or IgG (control). The ACTB1 promoter served as a negative control. C. Promoter enrichment of transcription factors (TFs) on the DREAM target genes ( Kif22 and Ncapd2 ). Each dataset was visualized on the UCSC genome browser. The dataset accession numbers were shown. Red boxes indicate the co-enrichment of Lin9 and Nfat on the promoters. P values were calculated using Student’s t -test; error bars, standard deviation (SD).

    Article Snippet: The following antibodies were used for immunoblotting: FOXM1 (Santa Cruz, sc-376471x, 1:1000), LIN9 (Santa Cruz, sc-398234, 1:2000), LIN54 (Bethyl, A303-799A-M,1:10000), FLAG M2 (Thermo, F1804, 1:20000) and alpha-tubulin (Cell signaling, 2144S, 1:5000).

    Techniques: Quantitative RT-PCR, Stable Transfection, Transduction, Control, Negative Control, Standard Deviation

    A, B. AlphaFold-multimer prediction (A) and corresponding predicted aligned error (PAE) plot (B) of the NFATc3-MuvB complex (LIN9, LIN37, LIN52, LIN54, and RBBP4). Structural confidence is represented by the predicted local distance difference test (plDDT) in (A). C, D. Schematic diagram of NFATc3-MuvB complex based on AlphaFold prediction and its visualization using PyMOL. E . NFATc3-LIN9 interaction, calculated by protein-protein interaction (PPI) analysis using PyMOL, 3.6 Å distance as a cutoff. F. Illustration of NFATc3-MuvB-FoxM1-MYBL2 complex predicted by AlphaFold; visualized by PyMOL. G. Interaction interface of NFATc3-FOXM1-LIN9-MYBL2 calculated by PPI analysis. NFATc3 and FOXM1 are highlighted with green and blue, respectively; 1.5 Å: The distance between the residues of K552 (NFATc3) and V233 (LIN9). H. Amino acid sequence alignment of NFATc3 and FOXM1 across diverse species . I. Co-immunoprecipitation (coIP) in A549 cells using IgG (control) or anti-NFATc3, followed by immunoblot (IB). J. Mapping of NFATc3 and FOXM1 binding sites on DREAM target gene promoters. Binding motifs for NFATc3 and FOXM1 were predicted using JASPAR position weight matrices (PWMs) and mapped using FIMO (Find Individual Motif Occurrences) ( P < 0.01). Bubble size (FIMO score) indicating the match strength between the DNA sequence and the transcription factor’s PWM. Larger bubbles represent stronger consensus match. K. Illustration of working model. In the presence of active NFATc3, NFATc3 is recruited to the DREAM target gene promoters via the LIN9/LIN37-based scaffold. CBP is likely to be co-enriched with NFATc3 for enhanced transactivation of the DREAM target genes.

    Journal: bioRxiv

    Article Title: NFATc3 Enhances DREAM Complex-Driven Transactivation

    doi: 10.64898/2026.01.12.699082

    Figure Lengend Snippet: A, B. AlphaFold-multimer prediction (A) and corresponding predicted aligned error (PAE) plot (B) of the NFATc3-MuvB complex (LIN9, LIN37, LIN52, LIN54, and RBBP4). Structural confidence is represented by the predicted local distance difference test (plDDT) in (A). C, D. Schematic diagram of NFATc3-MuvB complex based on AlphaFold prediction and its visualization using PyMOL. E . NFATc3-LIN9 interaction, calculated by protein-protein interaction (PPI) analysis using PyMOL, 3.6 Å distance as a cutoff. F. Illustration of NFATc3-MuvB-FoxM1-MYBL2 complex predicted by AlphaFold; visualized by PyMOL. G. Interaction interface of NFATc3-FOXM1-LIN9-MYBL2 calculated by PPI analysis. NFATc3 and FOXM1 are highlighted with green and blue, respectively; 1.5 Å: The distance between the residues of K552 (NFATc3) and V233 (LIN9). H. Amino acid sequence alignment of NFATc3 and FOXM1 across diverse species . I. Co-immunoprecipitation (coIP) in A549 cells using IgG (control) or anti-NFATc3, followed by immunoblot (IB). J. Mapping of NFATc3 and FOXM1 binding sites on DREAM target gene promoters. Binding motifs for NFATc3 and FOXM1 were predicted using JASPAR position weight matrices (PWMs) and mapped using FIMO (Find Individual Motif Occurrences) ( P < 0.01). Bubble size (FIMO score) indicating the match strength between the DNA sequence and the transcription factor’s PWM. Larger bubbles represent stronger consensus match. K. Illustration of working model. In the presence of active NFATc3, NFATc3 is recruited to the DREAM target gene promoters via the LIN9/LIN37-based scaffold. CBP is likely to be co-enriched with NFATc3 for enhanced transactivation of the DREAM target genes.

    Article Snippet: The following antibodies were used for immunoblotting: FOXM1 (Santa Cruz, sc-376471x, 1:1000), LIN9 (Santa Cruz, sc-398234, 1:2000), LIN54 (Bethyl, A303-799A-M,1:10000), FLAG M2 (Thermo, F1804, 1:20000) and alpha-tubulin (Cell signaling, 2144S, 1:5000).

    Techniques: Sequencing, Immunoprecipitation, Control, Western Blot, Binding Assay

    A. Ectopic expression and co-immunoprecipitation (coIP) in H1792 cells. Cells were transiently transfected with empty vector, control FLAG, or FLAG-tagged NFATc3. Cell lysates were immunoprecipitated with an anti-FLAG, followed by immunoblotting (IB) with antibodies against FOXM1, LIN9, and LIN54. B. Endogenous co-immunoprecipitation (coIP) in H1792 cells using IgG (control) or anti-NFATc3. Non-specific IgG served as a negative control.

    Journal: bioRxiv

    Article Title: NFATc3 Enhances DREAM Complex-Driven Transactivation

    doi: 10.64898/2026.01.12.699082

    Figure Lengend Snippet: A. Ectopic expression and co-immunoprecipitation (coIP) in H1792 cells. Cells were transiently transfected with empty vector, control FLAG, or FLAG-tagged NFATc3. Cell lysates were immunoprecipitated with an anti-FLAG, followed by immunoblotting (IB) with antibodies against FOXM1, LIN9, and LIN54. B. Endogenous co-immunoprecipitation (coIP) in H1792 cells using IgG (control) or anti-NFATc3. Non-specific IgG served as a negative control.

    Article Snippet: The following antibodies were used for immunoblotting: FOXM1 (Santa Cruz, sc-376471x, 1:1000), LIN9 (Santa Cruz, sc-398234, 1:2000), LIN54 (Bethyl, A303-799A-M,1:10000), FLAG M2 (Thermo, F1804, 1:20000) and alpha-tubulin (Cell signaling, 2144S, 1:5000).

    Techniques: Expressing, Immunoprecipitation, Transfection, Plasmid Preparation, Control, Western Blot, Negative Control