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tmp195 s8502  (Selleck Chemicals)


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    Selleck Chemicals tmp195 s8502
    ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), <t>TMP195</t> (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).
    Tmp195 S8502, supplied by Selleck Chemicals, 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/result/tmp195 s8502/product/Selleck Chemicals
    Average 93 stars, based on 6 article reviews
    tmp195 s8502 - by Bioz Stars, 2026-03
    93/100 stars

    Images

    1) Product Images from "Sorbate induces lysine sorbylation through noncanonical activities of class I HDACs to regulate the expression of inflammation genes"

    Article Title: Sorbate induces lysine sorbylation through noncanonical activities of class I HDACs to regulate the expression of inflammation genes

    Journal: Science Advances

    doi: 10.1126/sciadv.adv1071

    ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), TMP195 (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).
    Figure Legend Snippet: ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), TMP195 (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).

    Techniques Used: Enzymatic Assay, Western Blot, In Vitro, Recombinant, Cell Harvesting, Knockdown, Transfection, Incubation



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    ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), <t>TMP195</t> (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).
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    ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), <t>TMP195</t> (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).
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    ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), <t>TMP195</t> (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).
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    Image Search Results


    ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), TMP195 (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).

    Journal: Science Advances

    Article Title: Sorbate induces lysine sorbylation through noncanonical activities of class I HDACs to regulate the expression of inflammation genes

    doi: 10.1126/sciadv.adv1071

    Figure Lengend Snippet: ( A ) Schematic representation of HDAC-mediated Ksor and desorbylation. ( B ) Chemical inhibitor screening with extracted histones to identify a major class of HDACs that remove histone lysine sorbylation in cells. 293T cells were treated with 10 mM sorbate overnight. Sorbate-containing media were replaced with fresh media with or without various chemical inhibitors for 5 hours targeting different classes of HDACs including TSA (1 μM, lane 4), sodium butyrate (10 mM, lane 5), nicotinamide (25 mM, lane 6), UF010 (2 μM, lane 7), TMP195 (1 μM, lane 8), SIS17 (1 μM, lane 9), and MS275 (5 μM, lane 10) ( C ) Enzymatic assay and Western blot analysis demonstrating the in vitro desorbylase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from 293T cells treated with or without 10 mM sorbate and 40 mM sodium butyrate for 24 hours. ( D ) Western blotting analysis shows that HDAC inhibitor MS275 treatment dose-dependently inhibited Ksor in the presence of sorbate. 293T cells were treated with various concentrations of MS275 first for 30 min followed by the addition of potassium sorbate (2 mM) for the co-treatment of 6 hours before cell harvesting. ( E ) Enzymatic assay and Western blotting analysis demonstrating the in vitro sorbyltransferase activities of class I HDACs (HDAC1-3) with recombinant enzymes and extracted histones from regular 293T cells with or without sorbate. ( F ) siRNA knockdown and Western blot analysis demonstrating the endogenous activities of class I HDACs (HDAC1-3) in mediating global Ksor. SiRNAs targeting HDAC1, HDAC2, or HDAC3 were pooled and transfected to 293T cells for overnight incubation. Media were then replaced with fresh media with or without 10 mM sorbate treatment for overnight. Created in BioRender (Y. Chen, 2025; https://BioRender.com/a34b274 , https://BioRender.com/b79o565 , https://BioRender.com/r21b608 , and https://BioRender.com/n20b369 ).

    Article Snippet: SIS17 (S6687), UF010 (S5810), and TMP195 (S8502) were from Selleckchem (Houston, TX).

    Techniques: Enzymatic Assay, Western Blot, In Vitro, Recombinant, Cell Harvesting, Knockdown, Transfection, Incubation