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il1f6 il36a  (R&D Systems)


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    Structured Review

    R&D Systems il1f6 il36a
    Il1f6 Il36a, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/il1f6+il36a/pm30894050-268-33-34?v=R%26D+Systems
    Average 92 stars, based on 8 article reviews
    il1f6 il36a - by Bioz Stars, 2026-07
    92/100 stars

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    The activating process of IL-36α.

    Journal: Cancer Management and Research

    Article Title: The Pro-Tumor Biological Function of IL-36α Plays an Important Role in the Tumor Microenvironment of HCC

    doi: 10.2147/CMAR.S407123

    Figure Lengend Snippet: The activating process of IL-36α.

    Article Snippet: The CCK-8 kit, including human IL-36α/IL1F6 (IL36A) Kit, human IL-18, and IL-1β, was purchased from Solarbio, Beijing, China.

    Techniques:

    The expression of circulating ( A ) IL-36α, ( B ) AFP and ( C ) CEA transcribed. The X-axis represents different groups. The Y axis represents concentrations of these molecules (ng/mL). **** P <0.0001, ** P <0.01, * P <0.5.

    Journal: Cancer Management and Research

    Article Title: The Pro-Tumor Biological Function of IL-36α Plays an Important Role in the Tumor Microenvironment of HCC

    doi: 10.2147/CMAR.S407123

    Figure Lengend Snippet: The expression of circulating ( A ) IL-36α, ( B ) AFP and ( C ) CEA transcribed. The X-axis represents different groups. The Y axis represents concentrations of these molecules (ng/mL). **** P <0.0001, ** P <0.01, * P <0.5.

    Article Snippet: The CCK-8 kit, including human IL-36α/IL1F6 (IL36A) Kit, human IL-18, and IL-1β, was purchased from Solarbio, Beijing, China.

    Techniques: Expressing

    The expression of IL-36α in HCC and non-cancer tissues. ( A ) Results of HE staining at ×200 magnification. ( B ) IL-36α expression levels in non-cancer liver tissue (N), well-differentiated HCC (W), moderately differentiated HCC (M), and poorly differentiated HCC (P) measured by ELISA. The mean concentration of each group is represented by A. The horizontal axis represents the different groups, and the vertical axis represents the concentration of IL-36α (ng/mL). The IL-36α concentration in W, M, and P was significantly higher than that in N (*P<0.05, **P<0.01).

    Journal: Cancer Management and Research

    Article Title: The Pro-Tumor Biological Function of IL-36α Plays an Important Role in the Tumor Microenvironment of HCC

    doi: 10.2147/CMAR.S407123

    Figure Lengend Snippet: The expression of IL-36α in HCC and non-cancer tissues. ( A ) Results of HE staining at ×200 magnification. ( B ) IL-36α expression levels in non-cancer liver tissue (N), well-differentiated HCC (W), moderately differentiated HCC (M), and poorly differentiated HCC (P) measured by ELISA. The mean concentration of each group is represented by A. The horizontal axis represents the different groups, and the vertical axis represents the concentration of IL-36α (ng/mL). The IL-36α concentration in W, M, and P was significantly higher than that in N (*P<0.05, **P<0.01).

    Article Snippet: The CCK-8 kit, including human IL-36α/IL1F6 (IL36A) Kit, human IL-18, and IL-1β, was purchased from Solarbio, Beijing, China.

    Techniques: Expressing, Staining, Enzyme-linked Immunosorbent Assay, Concentration Assay

    Based on bioinformatics to investigate the prognosis of IL-36 in HCC. The correlation of IL-36R expression with prognosis of HCC patients. ( A ) IL-36R expression profile in different tumor types and normal (peri-tumor) tissues, with the height of each bar representing the median expression value. ( B ) Box plots showing IL-36R expression in liver hepatocellular carcinoma (LIHC) and normal (peri-tumor) tissues, obtained using the “Expression DIY” tab by GEPIA. The horizontal coordinate of T denotes LIHC tissues (n=369), while N denotes normal tissues (n=160). The color density of each block represents the median expression value, normalized by the maximum median expression value across all blocks. ( C ) The overall survival of LIHC patients with high and low IL-36R expression can be presented in the “Survival” tab, with a P value of 0.033 (<0.05).

    Journal: Cancer Management and Research

    Article Title: The Pro-Tumor Biological Function of IL-36α Plays an Important Role in the Tumor Microenvironment of HCC

    doi: 10.2147/CMAR.S407123

    Figure Lengend Snippet: Based on bioinformatics to investigate the prognosis of IL-36 in HCC. The correlation of IL-36R expression with prognosis of HCC patients. ( A ) IL-36R expression profile in different tumor types and normal (peri-tumor) tissues, with the height of each bar representing the median expression value. ( B ) Box plots showing IL-36R expression in liver hepatocellular carcinoma (LIHC) and normal (peri-tumor) tissues, obtained using the “Expression DIY” tab by GEPIA. The horizontal coordinate of T denotes LIHC tissues (n=369), while N denotes normal tissues (n=160). The color density of each block represents the median expression value, normalized by the maximum median expression value across all blocks. ( C ) The overall survival of LIHC patients with high and low IL-36R expression can be presented in the “Survival” tab, with a P value of 0.033 (<0.05).

    Article Snippet: The CCK-8 kit, including human IL-36α/IL1F6 (IL36A) Kit, human IL-18, and IL-1β, was purchased from Solarbio, Beijing, China.

    Techniques: Expressing, Blocking Assay

    The expression of IL-36α in different cell lines was investigated. ( A ) The expression levels of IL-36α were measured in Lo2 (normal liver cell), Huh7 (well-differentiated HCC cell), and HepG2 (poor-differentiated HCC cell), using ELISA. Higher expression of IL-36α was observed mainly in hepatocellular carcinoma cells. ( B ) The viability of the cell lines (Lo2, Huh7, and HepG2) was assessed after treatment with different concentrations of IL-36α (750, 500, 250, 125, and 62.5 ng/mL) for 24 hours. The viability of cells decreased with increasing IL-36α concentrations, with the greatest effect observed at 500 ng/mL. ( C and D ) The concentration of the treatment group was significantly lower than that of the blank control group. The scratch healing rate of lateral migration of HepG2 cells was assessed using a scratch healing experiment (*P<0.05).

    Journal: Cancer Management and Research

    Article Title: The Pro-Tumor Biological Function of IL-36α Plays an Important Role in the Tumor Microenvironment of HCC

    doi: 10.2147/CMAR.S407123

    Figure Lengend Snippet: The expression of IL-36α in different cell lines was investigated. ( A ) The expression levels of IL-36α were measured in Lo2 (normal liver cell), Huh7 (well-differentiated HCC cell), and HepG2 (poor-differentiated HCC cell), using ELISA. Higher expression of IL-36α was observed mainly in hepatocellular carcinoma cells. ( B ) The viability of the cell lines (Lo2, Huh7, and HepG2) was assessed after treatment with different concentrations of IL-36α (750, 500, 250, 125, and 62.5 ng/mL) for 24 hours. The viability of cells decreased with increasing IL-36α concentrations, with the greatest effect observed at 500 ng/mL. ( C and D ) The concentration of the treatment group was significantly lower than that of the blank control group. The scratch healing rate of lateral migration of HepG2 cells was assessed using a scratch healing experiment (*P<0.05).

    Article Snippet: The CCK-8 kit, including human IL-36α/IL1F6 (IL36A) Kit, human IL-18, and IL-1β, was purchased from Solarbio, Beijing, China.

    Techniques: Expressing, Enzyme-linked Immunosorbent Assay, Concentration Assay, Control, Migration

    IL-36α suppressed IL-1β and IL-18 expression in HepG2 cells in vitro. To test this, we set up blank control groups and treatment groups to measure the expression of IL-18 and IL-1β in HepG2 cells. The treatment group was treated with IL-36α (500 ng/mL) for 24 hours, while the control group was only added DMEM.

    Journal: Cancer Management and Research

    Article Title: The Pro-Tumor Biological Function of IL-36α Plays an Important Role in the Tumor Microenvironment of HCC

    doi: 10.2147/CMAR.S407123

    Figure Lengend Snippet: IL-36α suppressed IL-1β and IL-18 expression in HepG2 cells in vitro. To test this, we set up blank control groups and treatment groups to measure the expression of IL-18 and IL-1β in HepG2 cells. The treatment group was treated with IL-36α (500 ng/mL) for 24 hours, while the control group was only added DMEM.

    Article Snippet: The CCK-8 kit, including human IL-36α/IL1F6 (IL36A) Kit, human IL-18, and IL-1β, was purchased from Solarbio, Beijing, China.

    Techniques: Expressing, In Vitro, Control