eif4e (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc
eif4e
Eif4e, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1251 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+eif4e/S6+Ribosomal+Protein+Mouse+mAb/bio_rxiv__64898__2026__03__14__711799-139-36-37
Average 96 stars, based on 1251 article reviews
Eif4e, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1251 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+eif4e/S6+Ribosomal+Protein+Mouse+mAb/bio_rxiv__64898__2026__03__14__711799-139-36-37
Average 96 stars, based on 1251 article reviews
eif4e - by Bioz Stars,
2026-09
96/100 stars
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Western Blot:Article Title: Host Translational Control by Stress Granules Promotes Mycobacterium tuberculosis Pathogenesis Article Snippet: .. The following primary antibodies were used for immunoblot analysis: mouse anti‐Eif3η (SCT, sc‐137214), mouse anti‐G3bp1 (SCT, sc‐365338), mouse anti‐Lamp1 (SCT, sc‐20011), mouse anti‐Mfn1 (Invitrogen, MA5‐24789), mouse anti‐mTOR (CST, 4517), mouse anti‐Pabp1 (SCT, sc‐166381), mouse anti‐Raptor (SCT, sc‐81537), mouse anti‐Tomm20 (Sigma, WH0009804M1), rabbit anti‐4E‐BP1 (CST, 9644), rabbit anti‐4E‐BP1‐pT37/46 (CST, 2855), rabbit anti‐β‐Actin (CST, 4970), rabbit anti‐Drp1 (CST, 8570), rabbit anti‐Eif2α (CST, 5324), rabbit anti‐Eif2α‐pS51 (CST, 3597), rabbit other:Article Title: Targeted nanoencapsulation of tunicamycin reduces toxicity while improving its therapeutic effectiveness in pancreatic cancer cells Article Snippet: Incubation:Article Title: Identification of Raptor and GLI1 as USP37 substrates highlight its context-specific function in medulloblastoma cells Article Snippet: Cell pellets were washed with ice-cold PBS and lysed in mild lysis buffer (50mM Tris–HCl pH 7.5, 150mM NaCl, 1mM EDTA, 1% Triton X-100, 5 mM EDTA) containing protease inhibitor cocktail (Cat# 78429, Thermo Fisher Scientific) and phosphatase inhibitor (Sigma) and sonicated. .. Lysates were incubated with control mouse IgG, anti-USP37 (Cat# A300-927A, Thermo Fisher Scientific), anti-4EBP1 (Cat# 9644, Cell Signaling Technology, MA, USA), Article Title: Identification of Raptor and GLI1 as USP37 substrates highlight its context-specific function in medulloblastoma cells Article Snippet: Cell pellets were washed with ice-cold PBS and lysed in mild lysis buffer (50 mM Tris–HCl pH 7.5, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 5 mM EDTA) containing protease inhibitor cocktail (Cat# 78429, Thermo Fisher Scientific) and phosphatase inhibitor (Sigma) and sonicated. .. Lysates were incubated with control mouse IgG, anti-USP37 (Cat# A300-927A, Thermo Fisher Scientific), anti-4EBP1 (Cat# 9644, Cell Signaling Technology, MA, USA), Control:Article Title: Identification of Raptor and GLI1 as USP37 substrates highlight its context-specific function in medulloblastoma cells Article Snippet: Cell pellets were washed with ice-cold PBS and lysed in mild lysis buffer (50mM Tris–HCl pH 7.5, 150mM NaCl, 1mM EDTA, 1% Triton X-100, 5 mM EDTA) containing protease inhibitor cocktail (Cat# 78429, Thermo Fisher Scientific) and phosphatase inhibitor (Sigma) and sonicated. .. Lysates were incubated with control mouse IgG, anti-USP37 (Cat# A300-927A, Thermo Fisher Scientific), anti-4EBP1 (Cat# 9644, Cell Signaling Technology, MA, USA), Article Title: Identification of Raptor and GLI1 as USP37 substrates highlight its context-specific function in medulloblastoma cells Article Snippet: Cell pellets were washed with ice-cold PBS and lysed in mild lysis buffer (50 mM Tris–HCl pH 7.5, 150 mM NaCl, 1 mM EDTA, 1% Triton X-100, 5 mM EDTA) containing protease inhibitor cocktail (Cat# 78429, Thermo Fisher Scientific) and phosphatase inhibitor (Sigma) and sonicated. .. Lysates were incubated with control mouse IgG, anti-USP37 (Cat# A300-927A, Thermo Fisher Scientific), anti-4EBP1 (Cat# 9644, Cell Signaling Technology, MA, USA), Immunohistochemistry:Article Title: Vitamin D Regulates Olfactory Function via Dual Transcriptional and mTOR‐Dependent Translational Control of Synaptic Proteins Article Snippet: Capillary cartridges (Protein Simple, SM‐W004‐1), anti‐rabbit detection module chemiluminescence (Protein Simple DM‐001), anti‐mouse detection module chemiluminescence (Protein Simple DM‐002), and EZ standard pack (Protein Simple PS‐ST01EZ‐8) were used according to the manufacturer's instructions. .. The following antibodies were used (if not mentioned in the immunohistochemistry section): mouse anti‐β‐actin (1:200, Novus, NB600‐501), rabbit anti‐AKT (1:200, Cell Signaling Technology, 4691), rabbit anti‐p‐AKT (1:20, Cell Signaling Technology, 4060), rabbit |
![A , Western blot showing indicated proteins expression levels in YUMM1.1 cells expressing a shRNA control or targeting ASS1. HSP90 serves as a loading control. B , Western blot showing indicated proteins expression levels in YUMM1.7 cells expressing a shRNA control or targeting ASS1. HSP90 serves as a loading control. C , Western blot showing indicated proteins expression levels in YUMM2.1 cells expressing an ectopic empty vector or containing the open reading frame of ASS1. HSP90 serves as a loading control. D , Renilla over Firefly luminescent ratio quantification in YUMM1.1 cells expressing a shRNA control or targeting ASS1 (n=4; mean ± SEM). E , Renilla over Firefly luminescent ratio quantification in YUMM1.7 cells expressing a shRNA control or targeting ASS1 (n=3; mean ± SEM). F , Renilla over Firefly luminescent ratio quantification in YUMM2.1 cells expressing an ectopic empty vector or containing the open reading frame of ASS1 (n=3; mean ± SEM). G , Protein synthesis rates were determined in YUMM1.1 cells expressing a shRNA control or targeting ASS1. Cells were then pulsed for 30 min with [ 35 S]Cys/Met, and the incorporation of 35 S into proteins was quantified and normalized to the total protein amount. Cells treated 30 minutes with 100µg/mL of cycloheximide (CHX) are used as a positive control. The data are presented as the mean (n = 4). H , Protein synthesis rates were determined in YUMM1.7 cells expressing a shRNA control or targeting ASS1. Cells were then pulsed for 30 min with [ 35 S]Cys/Met, and the incorporation of 35 S into proteins was quantified and normalized to the total protein amount. Cells treated 30 minutes with 100µg/mL of cycloheximide (CHX) are used as a positive control. The data are presented as the mean (n = 3). I , Protein synthesis rates were determined in YUMM2.1 cells expressing an ectopic empty vector or containing the open reading frame of ASS1. Cells were then pulsed for 30 min with [ 35 S]Cys/Met, and the incorporation of 35 S into proteins was quantified and normalized to the total protein amount. Cells treated 30 minutes with 100µg/mL of cycloheximide (CHX) are used as a positive control. The data are presented as the mean (n = 3). J , Proximity Ligation Assay showing eiF4E/eiF4G interactions in YUMM1.1 cells expressing a shRNA control or targeting ASS1. Representative images are presented in the left panel, and quantifications are presented in the right panel. K , Proximity Ligation Assay showing eiF4E/eiF4G interactions in YUMM1.7 cells expressing a shRNA control or targeting ASS1. Representative images are presented in the left panel, and quantifications are presented in the right panel.](https://bio-rxiv-images-cdn.bioz.com/dois_ending_with_79/10__64898_slash_2026__03__17__712479/10__64898_slash_2026__03__17__712479___F3.large.jpg)