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human male xcl-1 ipscs  (XCell Science)

 
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    Structured Review

    XCell Science human male xcl-1 ipscs

    Human Male Xcl 1 Ipscs, supplied by XCell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+male+xcl-1+ipscs/human+parental+ipsc+line/pmc11831926-538-9-12
    Average 90 stars, based on 1 article reviews
    human male xcl-1 ipscs - by Bioz Stars, 2026-10
    90/100 stars

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    1) Product Images from "Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy"

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy

    Journal: Cell reports

    doi: 10.1016/j.celrep.2024.115205


    Figure Legend Snippet:

    Techniques Used: Virus, Recombinant, Protease Inhibitor, Membrane, Western Blot, Stripping, Modification, Transfection, Fractionation, Cell Culture, Lysis, Magnetic Beads, Electron Microscopy, Staining, Bicinchoninic Acid Protein Assay, Kinase Assay, LDH Cytotoxicity Assay, Mutagenesis, CyQUANT Assay, Sequencing, Negative Control, DNA Sequencing, Plasmid Preparation, Software, Imaging

    Related Articles

    Derivative Assay:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Extraction:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Virus:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Recombinant:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Protease Inhibitor:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Membrane:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Western Blot:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Stripping:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Modification:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Transfection:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Fractionation:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Cell Culture:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Lysis:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Magnetic Beads:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Electron Microscopy:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Staining:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Bicinchoninic Acid Protein Assay:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Kinase Assay:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    LDH Cytotoxicity Assay:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Mutagenesis:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    CyQUANT Assay:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Sequencing:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Negative Control:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    DNA Sequencing:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Plasmid Preparation:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Software:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Imaging:

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy
    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.



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    human male xcl-1 ipscs  (XCell Science)
    90
    XCell Science human male xcl-1 ipscs

    Human Male Xcl 1 Ipscs, supplied by XCell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+male+xcl-1+ipscs/human+parental+ipsc+line/pmc11831926-538-9-12
    Average 90 stars, based on 1 article reviews
    human male xcl-1 ipscs - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Journal: Cell reports

    Article Title: Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy

    doi: 10.1016/j.celrep.2024.115205

    Figure Lengend Snippet:

    Article Snippet: On Day 34 of differentiation iMNs derived from human male XCL-1 iPSCs (XCell Science) were subjected to proteotoxic stress by treatment with 0.5μM MG-132 (Millipore Sigma) plus 0.1% DMSO or 1μM VX-745 for 24 h. On day 35 cells were harvested and subjecyed to Sequential extraction of insoluble protein aggregates.

    Techniques: Virus, Recombinant, Protease Inhibitor, Membrane, Western Blot, Stripping, Modification, Transfection, Fractionation, Cell Culture, Lysis, Magnetic Beads, Electron Microscopy, Staining, Bicinchoninic Acid Protein Assay, Kinase Assay, LDH Cytotoxicity Assay, Mutagenesis, CyQUANT Assay, Sequencing, Negative Control, DNA Sequencing, Plasmid Preparation, Software, Imaging