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tgfβ2 treated groups  (MedChemExpress)


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    MedChemExpress tgfβ2 treated groups
    Proteomic analysis showed that expressions of TXNDC5 and ECM proteins were upregulated <t>in</t> <t>TGFβ2-treated</t> HTM cells. HTM cells were starved with serum-free DMEM/F12 medium for 24 hours and then treated with TGFβ2 (5 ng/mL) for 48 hours. (A) Changes of protein expression after TGFβ2 treatment in HTM cells were represented by volcano plots (≥1.2-fold difference: upregulated genes [ red ] and downregulated genes [ blue ]). Violin plots showed the TGFβ2-induced significant changes in TXNDC5 (B) , LN (C) , FN (D) , COL4A1 (E) , and COL4A2 (F) . ** P < 0.01; *** P < 0.001. (G) KEGG analysis indicated multiple metabolic and signal pathways, including ECM-receptor interaction, were changed markedly.
    Tgfβ2 Treated Groups, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tgfβ2 treated groups/product/MedChemExpress
    Average 94 stars, based on 15 article reviews
    tgfβ2 treated groups - by Bioz Stars, 2026-06
    94/100 stars

    Images

    1) Product Images from "TXNDC5 in POAG: Promoting Extracellular Matrix Protein Accumulation and Raising Intraocular Pressure"

    Article Title: TXNDC5 in POAG: Promoting Extracellular Matrix Protein Accumulation and Raising Intraocular Pressure

    Journal: Investigative Ophthalmology & Visual Science

    doi: 10.1167/iovs.67.4.46

    Proteomic analysis showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. HTM cells were starved with serum-free DMEM/F12 medium for 24 hours and then treated with TGFβ2 (5 ng/mL) for 48 hours. (A) Changes of protein expression after TGFβ2 treatment in HTM cells were represented by volcano plots (≥1.2-fold difference: upregulated genes [ red ] and downregulated genes [ blue ]). Violin plots showed the TGFβ2-induced significant changes in TXNDC5 (B) , LN (C) , FN (D) , COL4A1 (E) , and COL4A2 (F) . ** P < 0.01; *** P < 0.001. (G) KEGG analysis indicated multiple metabolic and signal pathways, including ECM-receptor interaction, were changed markedly.
    Figure Legend Snippet: Proteomic analysis showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. HTM cells were starved with serum-free DMEM/F12 medium for 24 hours and then treated with TGFβ2 (5 ng/mL) for 48 hours. (A) Changes of protein expression after TGFβ2 treatment in HTM cells were represented by volcano plots (≥1.2-fold difference: upregulated genes [ red ] and downregulated genes [ blue ]). Violin plots showed the TGFβ2-induced significant changes in TXNDC5 (B) , LN (C) , FN (D) , COL4A1 (E) , and COL4A2 (F) . ** P < 0.01; *** P < 0.001. (G) KEGG analysis indicated multiple metabolic and signal pathways, including ECM-receptor interaction, were changed markedly.

    Techniques Used: Expressing

    Western blot, qRT-PCR, and immunocytochemistry showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. (A) Concentration of TXNDC5 in the non-POAG ( n = 10) and POAG patients ( n = 7) in aqueous humor detected by ELISA. (B, C) TXNDC5 levels were not correlated with age and IOP in the non-POAG group and in POAG patients ( n = 7–8). (D) Representative images of Western blot analysis showing TGFβ2-induced changes in expressions of TXNDC5 and ECM proteins in HTM cells. (E–H) Quantitative analyses of Western blot of individual protein ( n = 4–6): TXNDC5 ( E ) , LN (F) , FN (G) , Col-IV (H) . Data are presented as mean ± SEM. (A) * P < 0.05 by unpaired, two-tailed t -test compared to non-POAG. (E–H) * P < 0.05; ** P < 0.01; *** P < 0.001 by unpaired, two-tailed t -test compared to control. (I) Representative images of immunofluorescence staining of TXNDC5, LN, FN, and COL-IV proteins in untreated control and TGFβ2-treated groups. Scale bars : 50 µm.
    Figure Legend Snippet: Western blot, qRT-PCR, and immunocytochemistry showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. (A) Concentration of TXNDC5 in the non-POAG ( n = 10) and POAG patients ( n = 7) in aqueous humor detected by ELISA. (B, C) TXNDC5 levels were not correlated with age and IOP in the non-POAG group and in POAG patients ( n = 7–8). (D) Representative images of Western blot analysis showing TGFβ2-induced changes in expressions of TXNDC5 and ECM proteins in HTM cells. (E–H) Quantitative analyses of Western blot of individual protein ( n = 4–6): TXNDC5 ( E ) , LN (F) , FN (G) , Col-IV (H) . Data are presented as mean ± SEM. (A) * P < 0.05 by unpaired, two-tailed t -test compared to non-POAG. (E–H) * P < 0.05; ** P < 0.01; *** P < 0.001 by unpaired, two-tailed t -test compared to control. (I) Representative images of immunofluorescence staining of TXNDC5, LN, FN, and COL-IV proteins in untreated control and TGFβ2-treated groups. Scale bars : 50 µm.

    Techniques Used: Western Blot, Quantitative RT-PCR, Immunocytochemistry, Concentration Assay, Enzyme-linked Immunosorbent Assay, Two Tailed Test, Control, Immunofluorescence, Staining



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    tgfβ2 treated groups  (MedChemExpress)
    94
    MedChemExpress tgfβ2 treated groups
    Proteomic analysis showed that expressions of TXNDC5 and ECM proteins were upregulated <t>in</t> <t>TGFβ2-treated</t> HTM cells. HTM cells were starved with serum-free DMEM/F12 medium for 24 hours and then treated with TGFβ2 (5 ng/mL) for 48 hours. (A) Changes of protein expression after TGFβ2 treatment in HTM cells were represented by volcano plots (≥1.2-fold difference: upregulated genes [ red ] and downregulated genes [ blue ]). Violin plots showed the TGFβ2-induced significant changes in TXNDC5 (B) , LN (C) , FN (D) , COL4A1 (E) , and COL4A2 (F) . ** P < 0.01; *** P < 0.001. (G) KEGG analysis indicated multiple metabolic and signal pathways, including ECM-receptor interaction, were changed markedly.
    Tgfβ2 Treated Groups, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tgfβ2 treated groups/product/MedChemExpress
    Average 94 stars, based on 1 article reviews
    tgfβ2 treated groups - by Bioz Stars, 2026-06
    94/100 stars
    		  Buy from Supplier

    Image Search Results


    Proteomic analysis showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. HTM cells were starved with serum-free DMEM/F12 medium for 24 hours and then treated with TGFβ2 (5 ng/mL) for 48 hours. (A) Changes of protein expression after TGFβ2 treatment in HTM cells were represented by volcano plots (≥1.2-fold difference: upregulated genes [ red ] and downregulated genes [ blue ]). Violin plots showed the TGFβ2-induced significant changes in TXNDC5 (B) , LN (C) , FN (D) , COL4A1 (E) , and COL4A2 (F) . ** P < 0.01; *** P < 0.001. (G) KEGG analysis indicated multiple metabolic and signal pathways, including ECM-receptor interaction, were changed markedly.

    Journal: Investigative Ophthalmology & Visual Science

    Article Title: TXNDC5 in POAG: Promoting Extracellular Matrix Protein Accumulation and Raising Intraocular Pressure

    doi: 10.1167/iovs.67.4.46

    Figure Lengend Snippet: Proteomic analysis showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. HTM cells were starved with serum-free DMEM/F12 medium for 24 hours and then treated with TGFβ2 (5 ng/mL) for 48 hours. (A) Changes of protein expression after TGFβ2 treatment in HTM cells were represented by volcano plots (≥1.2-fold difference: upregulated genes [ red ] and downregulated genes [ blue ]). Violin plots showed the TGFβ2-induced significant changes in TXNDC5 (B) , LN (C) , FN (D) , COL4A1 (E) , and COL4A2 (F) . ** P < 0.01; *** P < 0.001. (G) KEGG analysis indicated multiple metabolic and signal pathways, including ECM-receptor interaction, were changed markedly.

    Article Snippet: Both control and TGFβ2-treated groups were induced with 100 mg/mL CHX (MedChemExpress, Monmouth Junction, NJ, USA) to inhibit protein translation.

    Techniques: Expressing

    Western blot, qRT-PCR, and immunocytochemistry showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. (A) Concentration of TXNDC5 in the non-POAG ( n = 10) and POAG patients ( n = 7) in aqueous humor detected by ELISA. (B, C) TXNDC5 levels were not correlated with age and IOP in the non-POAG group and in POAG patients ( n = 7–8). (D) Representative images of Western blot analysis showing TGFβ2-induced changes in expressions of TXNDC5 and ECM proteins in HTM cells. (E–H) Quantitative analyses of Western blot of individual protein ( n = 4–6): TXNDC5 ( E ) , LN (F) , FN (G) , Col-IV (H) . Data are presented as mean ± SEM. (A) * P < 0.05 by unpaired, two-tailed t -test compared to non-POAG. (E–H) * P < 0.05; ** P < 0.01; *** P < 0.001 by unpaired, two-tailed t -test compared to control. (I) Representative images of immunofluorescence staining of TXNDC5, LN, FN, and COL-IV proteins in untreated control and TGFβ2-treated groups. Scale bars : 50 µm.

    Journal: Investigative Ophthalmology & Visual Science

    Article Title: TXNDC5 in POAG: Promoting Extracellular Matrix Protein Accumulation and Raising Intraocular Pressure

    doi: 10.1167/iovs.67.4.46

    Figure Lengend Snippet: Western blot, qRT-PCR, and immunocytochemistry showed that expressions of TXNDC5 and ECM proteins were upregulated in TGFβ2-treated HTM cells. (A) Concentration of TXNDC5 in the non-POAG ( n = 10) and POAG patients ( n = 7) in aqueous humor detected by ELISA. (B, C) TXNDC5 levels were not correlated with age and IOP in the non-POAG group and in POAG patients ( n = 7–8). (D) Representative images of Western blot analysis showing TGFβ2-induced changes in expressions of TXNDC5 and ECM proteins in HTM cells. (E–H) Quantitative analyses of Western blot of individual protein ( n = 4–6): TXNDC5 ( E ) , LN (F) , FN (G) , Col-IV (H) . Data are presented as mean ± SEM. (A) * P < 0.05 by unpaired, two-tailed t -test compared to non-POAG. (E–H) * P < 0.05; ** P < 0.01; *** P < 0.001 by unpaired, two-tailed t -test compared to control. (I) Representative images of immunofluorescence staining of TXNDC5, LN, FN, and COL-IV proteins in untreated control and TGFβ2-treated groups. Scale bars : 50 µm.

    Article Snippet: Both control and TGFβ2-treated groups were induced with 100 mg/mL CHX (MedChemExpress, Monmouth Junction, NJ, USA) to inhibit protein translation.

    Techniques: Western Blot, Quantitative RT-PCR, Immunocytochemistry, Concentration Assay, Enzyme-linked Immunosorbent Assay, Two Tailed Test, Control, Immunofluorescence, Staining