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antibodies against ly6c, nqo1, atf6, cleaved caspase 3, and tfam  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology antibodies against ly6c, nqo1, atf6, cleaved caspase 3, and tfam
    Antibodies Against Ly6c, Nqo1, Atf6, Cleaved Caspase 3, And Tfam, supplied by Santa Cruz Biotechnology, 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/cleaved+atf6/pm36064371-282-16-17?v=Santa+Cruz+Biotechnology
    Average 90 stars, based on 1 article reviews
    antibodies against ly6c, nqo1, atf6, cleaved caspase 3, and tfam - by Bioz Stars, 2026-07
    90/100 stars

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    a Quantification of conjugated ubiquitin levels (measured as median fluorescence levels of mono- and poly-ubiquitinylated conjugates ( n = 5), specific K48-linked poly-ubiquitinylated conjugates ( n = 3) or specific K63-linked poly-ubiquitinylated conjugates ( n = 3)) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. AU, arbitrary units. b Quantification of proteasome activity (measured as luminescence signal emitted upon the degradation of aminoluciferin-tagged peptide substrate Z-nLPnLD-aminoluciferin upon caspase-like proteolytic activity) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 4); RLU relative luminescence units. c Heatmap of transcript levels of molecular chaperones (BiP (HSPA5), eIF2α (EIF2A), ATF4, CHOP (DDIT3), XBP1, <t>ATF6,</t> heat shock protein 90 (HSP90B1), Derlin (DERL2/3), PDI (PDIA3/4/6), EDEM1/2/3, DNAJB9, calreticulin (CALR) and calnexin (CANX)) involved in the unfolded protein response (UPR) assessed by bulk RNA sequencing of control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 3). Color scale: red, high expression; blue, low expression. d – h Representative immunoblot and densitometric quantification of BiP ( d ; n = 6), ATF4 ( e ; n = 4), CHOP ( e ; n = 3), spliced XBP1 (XBP1s; see black arrowhead) ( f ; n = 3), cleaved ATF6 (cATF6) ( g ; n = 7) and ERp72 ( h ; n = 4) protein levels in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. GAPDH was used as a loading control. Data are mean ± s.e.m. Statistics: ANOVA ( a , b–h ); * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001.
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    Average 90 stars, based on 1 article reviews
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    antibodies for chop, atf4, atf6, phosphorylated-eif2a, xbp1s, cleaved caspase-3 and gapdh  (Cell Signaling Technology Inc)
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    Cell Signaling Technology Inc antibodies for chop, atf4, atf6, phosphorylated-eif2a, xbp1s, cleaved caspase-3 and gapdh
    a Quantification of conjugated ubiquitin levels (measured as median fluorescence levels of mono- and poly-ubiquitinylated conjugates ( n = 5), specific K48-linked poly-ubiquitinylated conjugates ( n = 3) or specific K63-linked poly-ubiquitinylated conjugates ( n = 3)) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. AU, arbitrary units. b Quantification of proteasome activity (measured as luminescence signal emitted upon the degradation of aminoluciferin-tagged peptide substrate Z-nLPnLD-aminoluciferin upon caspase-like proteolytic activity) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 4); RLU relative luminescence units. c Heatmap of transcript levels of molecular chaperones (BiP (HSPA5), eIF2α (EIF2A), ATF4, CHOP (DDIT3), XBP1, <t>ATF6,</t> heat shock protein 90 (HSP90B1), Derlin (DERL2/3), PDI (PDIA3/4/6), EDEM1/2/3, DNAJB9, calreticulin (CALR) and calnexin (CANX)) involved in the unfolded protein response (UPR) assessed by bulk RNA sequencing of control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 3). Color scale: red, high expression; blue, low expression. d – h Representative immunoblot and densitometric quantification of BiP ( d ; n = 6), ATF4 ( e ; n = 4), CHOP ( e ; n = 3), spliced XBP1 (XBP1s; see black arrowhead) ( f ; n = 3), cleaved ATF6 (cATF6) ( g ; n = 7) and ERp72 ( h ; n = 4) protein levels in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. GAPDH was used as a loading control. Data are mean ± s.e.m. Statistics: ANOVA ( a , b–h ); * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001.
    Antibodies For Chop, Atf4, Atf6, Phosphorylated Eif2a, Xbp1s, Cleaved Caspase 3 And Gapdh, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    a Quantification of conjugated ubiquitin levels (measured as median fluorescence levels of mono- and poly-ubiquitinylated conjugates ( n = 5), specific K48-linked poly-ubiquitinylated conjugates ( n = 3) or specific K63-linked poly-ubiquitinylated conjugates ( n = 3)) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. AU, arbitrary units. b Quantification of proteasome activity (measured as luminescence signal emitted upon the degradation of aminoluciferin-tagged peptide substrate Z-nLPnLD-aminoluciferin upon caspase-like proteolytic activity) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 4); RLU relative luminescence units. c Heatmap of transcript levels of molecular chaperones (BiP (HSPA5), eIF2α (EIF2A), ATF4, CHOP (DDIT3), XBP1, ATF6, heat shock protein 90 (HSP90B1), Derlin (DERL2/3), PDI (PDIA3/4/6), EDEM1/2/3, DNAJB9, calreticulin (CALR) and calnexin (CANX)) involved in the unfolded protein response (UPR) assessed by bulk RNA sequencing of control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 3). Color scale: red, high expression; blue, low expression. d – h Representative immunoblot and densitometric quantification of BiP ( d ; n = 6), ATF4 ( e ; n = 4), CHOP ( e ; n = 3), spliced XBP1 (XBP1s; see black arrowhead) ( f ; n = 3), cleaved ATF6 (cATF6) ( g ; n = 7) and ERp72 ( h ; n = 4) protein levels in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. GAPDH was used as a loading control. Data are mean ± s.e.m. Statistics: ANOVA ( a , b–h ); * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001.

    Journal: Communications Biology

    Article Title: The gluconeogenesis enzyme PCK2 has a non-enzymatic role in proteostasis in endothelial cells

    doi: 10.1038/s42003-024-06186-6

    Figure Lengend Snippet: a Quantification of conjugated ubiquitin levels (measured as median fluorescence levels of mono- and poly-ubiquitinylated conjugates ( n = 5), specific K48-linked poly-ubiquitinylated conjugates ( n = 3) or specific K63-linked poly-ubiquitinylated conjugates ( n = 3)) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. AU, arbitrary units. b Quantification of proteasome activity (measured as luminescence signal emitted upon the degradation of aminoluciferin-tagged peptide substrate Z-nLPnLD-aminoluciferin upon caspase-like proteolytic activity) in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 4); RLU relative luminescence units. c Heatmap of transcript levels of molecular chaperones (BiP (HSPA5), eIF2α (EIF2A), ATF4, CHOP (DDIT3), XBP1, ATF6, heat shock protein 90 (HSP90B1), Derlin (DERL2/3), PDI (PDIA3/4/6), EDEM1/2/3, DNAJB9, calreticulin (CALR) and calnexin (CANX)) involved in the unfolded protein response (UPR) assessed by bulk RNA sequencing of control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose ( n = 3). Color scale: red, high expression; blue, low expression. d – h Representative immunoblot and densitometric quantification of BiP ( d ; n = 6), ATF4 ( e ; n = 4), CHOP ( e ; n = 3), spliced XBP1 (XBP1s; see black arrowhead) ( f ; n = 3), cleaved ATF6 (cATF6) ( g ; n = 7) and ERp72 ( h ; n = 4) protein levels in control and PCK2 KD1 ECs in 5.5 versus 0 mM glucose. GAPDH was used as a loading control. Data are mean ± s.e.m. Statistics: ANOVA ( a , b–h ); * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001.

    Article Snippet: We used primary antibodies against: PCK2 (D3E11, Cell Signaling Technology #8565, dilution 1:1,000), GAPDH (14C10, Cell Signaling Technology #2118, dilution 1:1,000), LC3B (Abcam #ab51520, dilution 1:3,000), p62/SQSTM1 (Sigma-Aldrich #P0067, dilution 1:1,000), BiP (C50B12, Cell Signaling Technology #3177, dilution 1:1,000), ATF4 (D4B8, Cell Signaling Technology #11815, dilution 1:1,000), CHOP (L63F7, Cell Signaling Technology #2895, dilution 1:1,000), VDAC1 (B-6, Santa Cruz Biotechnology #sc390996, dilution 1:200), SOD1 (Enzo Life Sciences #ADI-SOD-100, dilution 1:1,000), phospho-S6 (Ser235/236) (D57.2.E2, Cell Signaling Technology #4858, dilution 1:2,000), S6 (5G10, Cell Signaling Technology #2217, dilution 1:1,000), phospho-p70S6K (T389) (Cell Signaling Technology #9205, dilution 1:1,000), p70S6K (Cell Signaling Technology #9202, dilution 1:1,000), cleaved ATF6 (Abcam #ab122897, dilution 1:500), spliced XBP1 (XBP1s) (Novus Biologicals #NBP1-77681, dilution 1:1,000), ERp72 (D70D12, Cell Signaling Technology #5033, dilution 1:1,000).

    Techniques: Fluorescence, Activity Assay, RNA Sequencing Assay, Expressing, Western Blot