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rabbit anti p eif2 α pabs  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit anti p eif2 α pabs
    pCP312R promotes the phosphorylation of PERK and <t>eIF2</t> α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis <t>using</t> <t>anti-Flag,</t> <t>anti-p-eIF2</t> α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.
    Rabbit Anti P Eif2 α Pabs, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1405 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 96 stars, based on 1405 article reviews
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    Images

    1) Product Images from "The CP312R protein of African swine fever virus inhibits host protein translation via the BiP/PERK/eIF2 α pathway"

    Article Title: The CP312R protein of African swine fever virus inhibits host protein translation via the BiP/PERK/eIF2 α pathway

    Journal: Veterinary Research

    doi: 10.1186/s13567-025-01688-5

    pCP312R promotes the phosphorylation of PERK and eIF2 α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis using anti-Flag, anti-p-eIF2 α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.
    Figure Legend Snippet: pCP312R promotes the phosphorylation of PERK and eIF2 α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis using anti-Flag, anti-p-eIF2 α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.

    Techniques Used: Phospho-proteomics, Transfection, Western Blot, Incubation, Inhibition

    Related Articles

    other:

    Article Title: Mechanism of endoplasmic reticulum stress-induced vascular endothelial dysfunction
    Article Snippet: 53 Western blot analysis for P-eNOS, T-eNOS, P-PERK, T-PERK, BiP(GRP78), P-eIF2-α, T-eIF2-α, CHOP, P-p38 and T-p38MAPK, P-ERK1/2 and T-ERK1/2 (1:1000 dilution, Cell Signaling Technology, Inc, USA), and ATF6, HuR or β-actin (1:500 dilution, Santa Cruz Biotechnology, Inc) was performed using specific antibodies as previously described.

    Article Title: The envelope proteins from SARS-CoV-2 and SARS-CoV potently reduce the infectivity of human immunodeficiency virus type 1 (HIV-1)
    Article Snippet: The cells were harvested at 48 h pt and equal amounts of proteins were analyzed by western blot for p-eIF2-α or total eIF2-α (both antibodies were obtained from Cell Signaling).

    Article Title: The Envelope Proteins from SARS-CoV-2 and SARS-CoV Potently Reduce the Infectivity of Human Immunodeficiency Virus type 1 (HIV-1)
    Article Snippet: The cells were harvested at 48 h pt and equal amounts of proteins were analyzed by western blot for p-eIF2-α or total eIF2-α (both antibodies were obtained from Cell Signaling).



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    pCP312R promotes the phosphorylation of PERK and <t>eIF2</t> α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis <t>using</t> <t>anti-Flag,</t> <t>anti-p-eIF2</t> α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.
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    pCP312R promotes the phosphorylation of PERK and <t>eIF2</t> α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis <t>using</t> <t>anti-Flag,</t> <t>anti-p-eIF2</t> α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.
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    pCP312R promotes the phosphorylation of PERK and <t>eIF2</t> α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis <t>using</t> <t>anti-Flag,</t> <t>anti-p-eIF2</t> α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.
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    pCP312R promotes the phosphorylation of PERK and <t>eIF2</t> α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis <t>using</t> <t>anti-Flag,</t> <t>anti-p-eIF2</t> α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.
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    Cell Signaling Technology Inc p eif2 α s52
    Reagents and tools table
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    Image Search Results


    pCP312R promotes the phosphorylation of PERK and eIF2 α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis using anti-Flag, anti-p-eIF2 α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.

    Journal: Veterinary Research

    Article Title: The CP312R protein of African swine fever virus inhibits host protein translation via the BiP/PERK/eIF2 α pathway

    doi: 10.1186/s13567-025-01688-5

    Figure Lengend Snippet: pCP312R promotes the phosphorylation of PERK and eIF2 α . A pCP312R promotes the phosphorylation of PERK in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 24 h post-transfection (hpt), the cells were collected for western blotting analysis using anti-Flag, anti-p-PERK (Thr982), anti-PERK, or anti- β -actin antibodies. B pCP312R promotes eIF2 α phosphorylation in a dose-dependent manner. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 0.5, 1, 1.5, or 2 μg). At 12 hpt, the cells were incubated with 300 nM thapsigargin (Tg) for 8 h, and then the cells were collected for western blotting analysis using anti-Flag, anti-p-eIF2 α , anti-eIF2 α , or anti- β -actin antibodies. C Inhibition of the cellular protein synthesis by pCP312R is attenuated by ISRIB. HEK293T cells were transfected with an increasing amount of pCA-CP312R-Flag (0, 1, 1.5, 2, or 2.5 μg). At 12 hpt, the cells were treated with ISRIB (0.5 μM) for another 12 h. The cells were pulsed with 3 μM puromycin for 30 min, followed by western blotting analysis using anti-Flag, anti-puromycin, or anti- β -actin antibodies.

    Article Snippet: Mouse anti-p72 monoclonal antibody (MAb) (catalog no. Anti PPA 1BC11, INGENASA), mouse anti-puromycin MAb (catalog no. MABE343, Sigma-Aldrich), rabbit anti- β -actin PAbs (catalog no. AC026, ABclonal), mouse anti-Flag MAb (catalog no. M8823, Sigma-Aldrich), mouse anti-GST MAb (catalog no. K200006M, Solarbio), rabbit anti-Myc PAbs (catalog no. YN5506, ImmunoWay), rabbit anti-KDEL PAbs (catalog no. ab214714, Abcam), rabbit anti-BiP PAbs (catalog no. A0241, ABclonal), mouse anti-PERK MAb (catalog no. 3192S, CST), rabbit anti-p-PERK PAbs (catalog no. BS66100, Bioworld), rabbit anti-p-eIF2 α PAbs (catalog no. 3398S, CST), and rabbit anti-eIF2 α PAbs (catalog no. 9722S, CST) are commercially available.

    Techniques: Phospho-proteomics, Transfection, Western Blot, Incubation, Inhibition

    Reagents and tools table

    Journal: The EMBO Journal

    Article Title: The integrated stress response drives MET oncogene overexpression in cancers

    doi: 10.1038/s44318-024-00338-4

    Figure Lengend Snippet: Reagents and tools table

    Article Snippet: P-eIF2 α -S52 , Cell Signalling Technology , 3398.

    Techniques: Recombinant, Sequencing, Transfection, Western Blot, Luciferase, CyQUANT Assay, Proliferation Assay, Plasmid Preparation, Software