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rabbit anti β actin 5057s  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti β actin 5057s
    Rabbit Anti β Actin 5057s, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 100 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+%CE%B2+actin+5057s/beta-Actin+Rabbit+mAb/pm41932973-83-10-16
    Average 94 stars, based on 100 article reviews
    rabbit anti β actin 5057s - by Bioz Stars, 2026-10
    94/100 stars

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    Article Title: ORF3 protein of porcine circovirus type 2 induced RIPK3 phosphorylation-driven autophagy to promote viral replication.
    Article Snippet: Rabbit anti-RIPK3 (10188T), rabbit anti-LC3B (2775S), rabbit anti-GAPDH (2118S), and rabbit anti-β-Actin (5057S) were purchased from Cell Signaling Technology (CST, Beverly, MA, USA).



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    The phagocytosis of macrophages by rCFP-10 is dependent on mTORC2 activity. A The level of p-mTOR, p-S6 K, p-AKT, p-S6, and <t>β-actin</t> treated with rCFP-10 for 2 h in J774A.1 and BMMϕ were determined by western blot analysis. B Bar charts show level of p-mTOR, p-S6 K, p-AKT, p-S6 in J774A.1 cells and BMMϕ with indicated treat-ments. Data shown are representative of at least three experiments. C Phagocytosis of J774A.1 cells and BMMϕ treated with 100 µg/ml rCFP-10 for 2 h in the presence of rapamycin and Torin was determined by flow cytometry. D , E Bar charts show the phagocytosis percentage in J774A.1 cells ( D ) and BMMϕ ( E ) with indicated treatments. Data shown are representative of at least three experiments. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t-test
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    The phagocytosis of macrophages by rCFP-10 is dependent on mTORC2 activity. A The level of p-mTOR, p-S6 K, p-AKT, p-S6, and <t>β-actin</t> treated with rCFP-10 for 2 h in J774A.1 and BMMϕ were determined by western blot analysis. B Bar charts show level of p-mTOR, p-S6 K, p-AKT, p-S6 in J774A.1 cells and BMMϕ with indicated treat-ments. Data shown are representative of at least three experiments. C Phagocytosis of J774A.1 cells and BMMϕ treated with 100 µg/ml rCFP-10 for 2 h in the presence of rapamycin and Torin was determined by flow cytometry. D , E Bar charts show the phagocytosis percentage in J774A.1 cells ( D ) and BMMϕ ( E ) with indicated treatments. Data shown are representative of at least three experiments. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t-test
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    Image Search Results


    The phagocytosis of macrophages by rCFP-10 is dependent on mTORC2 activity. A The level of p-mTOR, p-S6 K, p-AKT, p-S6, and β-actin treated with rCFP-10 for 2 h in J774A.1 and BMMϕ were determined by western blot analysis. B Bar charts show level of p-mTOR, p-S6 K, p-AKT, p-S6 in J774A.1 cells and BMMϕ with indicated treat-ments. Data shown are representative of at least three experiments. C Phagocytosis of J774A.1 cells and BMMϕ treated with 100 µg/ml rCFP-10 for 2 h in the presence of rapamycin and Torin was determined by flow cytometry. D , E Bar charts show the phagocytosis percentage in J774A.1 cells ( D ) and BMMϕ ( E ) with indicated treatments. Data shown are representative of at least three experiments. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t-test

    Journal: BMC Immunology

    Article Title: mTORC2 is crucial for regulating the recombinant Mycobacterium tuberculosis CFP-10 protein-induced phagocytosis in macrophages

    doi: 10.1186/s12865-025-00715-6

    Figure Lengend Snippet: The phagocytosis of macrophages by rCFP-10 is dependent on mTORC2 activity. A The level of p-mTOR, p-S6 K, p-AKT, p-S6, and β-actin treated with rCFP-10 for 2 h in J774A.1 and BMMϕ were determined by western blot analysis. B Bar charts show level of p-mTOR, p-S6 K, p-AKT, p-S6 in J774A.1 cells and BMMϕ with indicated treat-ments. Data shown are representative of at least three experiments. C Phagocytosis of J774A.1 cells and BMMϕ treated with 100 µg/ml rCFP-10 for 2 h in the presence of rapamycin and Torin was determined by flow cytometry. D , E Bar charts show the phagocytosis percentage in J774A.1 cells ( D ) and BMMϕ ( E ) with indicated treatments. Data shown are representative of at least three experiments. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t-test

    Article Snippet: β-Actin (D6 A8) Rabbit mAb, Phospho-mTOR (Ser2448) XP ® Rabbit mAb, Phospho-S6 Ribosomal Protei (Ser235/236) (D57.2.2E) XP ® Rabbit mAb, Phospho-p70 S6 Kinase (Thr389) (D5U1O) Rabbit mAb, and Phospho-Akt (Ser473) (D9E) XP ® Rabbit mAb were purchased from Cell Signaling Technology (CST).

    Techniques: Activity Assay, Western Blot, Flow Cytometry

    The expression level of tmem199, which is involved in lysosome acidification, in macrophages treated with rCFP-10 is reliant on the activity of mTORC2. A , B Heapmap of transcriptional profiles of J774A.1 cells and BMMϕ with or without rCFP-10 treatment (PBS: n = 3; rCFP-10: n = 3). Gene expressions are presented as log2 fluorescence intensity centered and scaled (blue and red keys) grouped according to the product functions. C Transcrption of Tmem199 was relative to β-actin in the J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment. D Expression of TMEM199 in the J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment determined by flow cytometry. E Bar charts show level of TMEM199 in the J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t -test

    Journal: BMC Immunology

    Article Title: mTORC2 is crucial for regulating the recombinant Mycobacterium tuberculosis CFP-10 protein-induced phagocytosis in macrophages

    doi: 10.1186/s12865-025-00715-6

    Figure Lengend Snippet: The expression level of tmem199, which is involved in lysosome acidification, in macrophages treated with rCFP-10 is reliant on the activity of mTORC2. A , B Heapmap of transcriptional profiles of J774A.1 cells and BMMϕ with or without rCFP-10 treatment (PBS: n = 3; rCFP-10: n = 3). Gene expressions are presented as log2 fluorescence intensity centered and scaled (blue and red keys) grouped according to the product functions. C Transcrption of Tmem199 was relative to β-actin in the J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment. D Expression of TMEM199 in the J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment determined by flow cytometry. E Bar charts show level of TMEM199 in the J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t -test

    Article Snippet: β-Actin (D6 A8) Rabbit mAb, Phospho-mTOR (Ser2448) XP ® Rabbit mAb, Phospho-S6 Ribosomal Protei (Ser235/236) (D57.2.2E) XP ® Rabbit mAb, Phospho-p70 S6 Kinase (Thr389) (D5U1O) Rabbit mAb, and Phospho-Akt (Ser473) (D9E) XP ® Rabbit mAb were purchased from Cell Signaling Technology (CST).

    Techniques: Expressing, Activity Assay, Fluorescence, Flow Cytometry

    mTORC2 activity was crucial for the expression of genes involved in TLR signaling. A , B Heapmap of transcriptional profiles of J774A.1 cells and BMMϕ with or without rCFP-10 treatment (PBS: n = 3; rCFP-10: n = 3). Gene expressions are presented as log2 fluorescence intensity centered and scaled (blue and red keys) grouped according to the product functions. A The TLR signaling pathway is expressed in the J774A.1 cell. B The TLR signaling pathway is expressed in the BMMϕ. C-E Transcription of Myd88, TBK1, TLR2 was relative to β-actin in J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment. F Production of the pro-inflammatory cytokine TNF-α in the supernatant of J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 4 h in the presence or absence of rapamycin and Torin1 pretreatment. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t -test

    Journal: BMC Immunology

    Article Title: mTORC2 is crucial for regulating the recombinant Mycobacterium tuberculosis CFP-10 protein-induced phagocytosis in macrophages

    doi: 10.1186/s12865-025-00715-6

    Figure Lengend Snippet: mTORC2 activity was crucial for the expression of genes involved in TLR signaling. A , B Heapmap of transcriptional profiles of J774A.1 cells and BMMϕ with or without rCFP-10 treatment (PBS: n = 3; rCFP-10: n = 3). Gene expressions are presented as log2 fluorescence intensity centered and scaled (blue and red keys) grouped according to the product functions. A The TLR signaling pathway is expressed in the J774A.1 cell. B The TLR signaling pathway is expressed in the BMMϕ. C-E Transcription of Myd88, TBK1, TLR2 was relative to β-actin in J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 2 h in the presence or absence of rapamycin and Torin1 pretreatment. F Production of the pro-inflammatory cytokine TNF-α in the supernatant of J774A.1 cells after treatment with 100 µg/ml of rCFP-10 treatment for 4 h in the presence or absence of rapamycin and Torin1 pretreatment. *: P < 0.05; **: P < 0.01; ***: P < 0.001; ns = no significant was determined by Student t -test

    Article Snippet: β-Actin (D6 A8) Rabbit mAb, Phospho-mTOR (Ser2448) XP ® Rabbit mAb, Phospho-S6 Ribosomal Protei (Ser235/236) (D57.2.2E) XP ® Rabbit mAb, Phospho-p70 S6 Kinase (Thr389) (D5U1O) Rabbit mAb, and Phospho-Akt (Ser473) (D9E) XP ® Rabbit mAb were purchased from Cell Signaling Technology (CST).

    Techniques: Activity Assay, Expressing, Fluorescence