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alex human hepatoma cell line  (JCRB Cell Bank)

 
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    JCRB Cell Bank alex human hepatoma cell line
    Stromal cells increased p-STAT3 and CTGF expression and cell growth in hepatoma <t>cells.</t> <t>HepG2</t> or <t>Alex</t> cells were transfected with STAT3 siRNA or control siRNA ( A-B ). WST-8 assay ( A ) and CTGF mRNA expression ( B ) of HepG2 or Alex cells after siRNA transfection. Total RNA was collected 48 hours after siRNA transfection. HepG2 or Alex cells were incubated in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells, using Transwell insert system ( C-G ). THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculturing. Total proteins and RNA were collected after 24 hours of incubation ( C, E, F ). C , Western blot showing protein expression of HepG2 or Alex cells. D , WST-8 assay of HepG2 or Alex cells in coculture at the indicated time points. HepG2 or Alex cells were transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours before coculturing ( E-G ). E , Western blot showing protein expression and qPCR showing CTGF mRNA expression in HepG2 or Alex cells transfected with STAT3 siRNA or control siRNA. F , Western blot and CTGF mRNA expression in HepG2 or Alex cells transfected with gp130 siRNA or control siRNA. G , WST-8 assay of HepG2 or Alex cells transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours after incubation (n = 3-4). ∗ , †, ‡, § P < .05 vs control.
    Alex Human Hepatoma Cell Line, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/alex human hepatoma cell line/product/JCRB Cell Bank
    Average 90 stars, based on 1 article reviews
    alex human hepatoma cell line - by Bioz Stars, 2026-05
    90/100 stars

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    1) Product Images from "STAT3 is Activated by CTGF-mediated Tumor-stroma Cross Talk to Promote HCC Progression"

    Article Title: STAT3 is Activated by CTGF-mediated Tumor-stroma Cross Talk to Promote HCC Progression

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    doi: 10.1016/j.jcmgh.2022.09.006

    Stromal cells increased p-STAT3 and CTGF expression and cell growth in hepatoma cells. HepG2 or Alex cells were transfected with STAT3 siRNA or control siRNA ( A-B ). WST-8 assay ( A ) and CTGF mRNA expression ( B ) of HepG2 or Alex cells after siRNA transfection. Total RNA was collected 48 hours after siRNA transfection. HepG2 or Alex cells were incubated in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells, using Transwell insert system ( C-G ). THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculturing. Total proteins and RNA were collected after 24 hours of incubation ( C, E, F ). C , Western blot showing protein expression of HepG2 or Alex cells. D , WST-8 assay of HepG2 or Alex cells in coculture at the indicated time points. HepG2 or Alex cells were transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours before coculturing ( E-G ). E , Western blot showing protein expression and qPCR showing CTGF mRNA expression in HepG2 or Alex cells transfected with STAT3 siRNA or control siRNA. F , Western blot and CTGF mRNA expression in HepG2 or Alex cells transfected with gp130 siRNA or control siRNA. G , WST-8 assay of HepG2 or Alex cells transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours after incubation (n = 3-4). ∗ , †, ‡, § P < .05 vs control.
    Figure Legend Snippet: Stromal cells increased p-STAT3 and CTGF expression and cell growth in hepatoma cells. HepG2 or Alex cells were transfected with STAT3 siRNA or control siRNA ( A-B ). WST-8 assay ( A ) and CTGF mRNA expression ( B ) of HepG2 or Alex cells after siRNA transfection. Total RNA was collected 48 hours after siRNA transfection. HepG2 or Alex cells were incubated in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells, using Transwell insert system ( C-G ). THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculturing. Total proteins and RNA were collected after 24 hours of incubation ( C, E, F ). C , Western blot showing protein expression of HepG2 or Alex cells. D , WST-8 assay of HepG2 or Alex cells in coculture at the indicated time points. HepG2 or Alex cells were transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours before coculturing ( E-G ). E , Western blot showing protein expression and qPCR showing CTGF mRNA expression in HepG2 or Alex cells transfected with STAT3 siRNA or control siRNA. F , Western blot and CTGF mRNA expression in HepG2 or Alex cells transfected with gp130 siRNA or control siRNA. G , WST-8 assay of HepG2 or Alex cells transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours after incubation (n = 3-4). ∗ , †, ‡, § P < .05 vs control.

    Techniques Used: Expressing, Transfection, Control, Incubation, Western Blot

    IL-6 family cytokines increased p-STAT3 and CTGF expression in hepatoma cells and enhanced cell proliferation. Concentrations of IL-6, LIF, and OSM in the culture supernatant ( A ). Culture supernatant was collected 24 hours after the initiation of HepG2, Alex, LX-2, THP-1, MTA, and TMNK-1 cell monoculture. IL-6, LIF, or OSM concentration was measured by enzyme-linked immunosorbent assay. THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation, and the culture medium was replaced with PMA-free medium 24 hours before supernatant collection. HepG2 cells and Alex cells were treated with recombinant proteins of IL-6 (20 ng/mL), LIF (1:1000), or OSM (20 ng/mL) ( B-D ). Cells were serum-starved for 16 hours before the addition of recombinant proteins. B , Protein expression 1 hour after recombinant protein treatment. C , mRNA expression of CTGF 3 hours after recombinant protein treatment. D , WST-8 assay at the indicated time points after treatment with recombinant proteins. HepG2 cells and Alex cells were transfected with gp130 siRNA, STAT3 siRNA, or control siRNA 48 hours before the addition of recombinant proteins ( E-F ). Recombinant proteins were added 16 hours after serum starvation. E , mRNA expression of CTGF 3 hours after treatment with recombinant proteins. F , WST-8 assay at the indicated time points after recombinant protein treatment (n = 3-4). ∗ P < .05.
    Figure Legend Snippet: IL-6 family cytokines increased p-STAT3 and CTGF expression in hepatoma cells and enhanced cell proliferation. Concentrations of IL-6, LIF, and OSM in the culture supernatant ( A ). Culture supernatant was collected 24 hours after the initiation of HepG2, Alex, LX-2, THP-1, MTA, and TMNK-1 cell monoculture. IL-6, LIF, or OSM concentration was measured by enzyme-linked immunosorbent assay. THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation, and the culture medium was replaced with PMA-free medium 24 hours before supernatant collection. HepG2 cells and Alex cells were treated with recombinant proteins of IL-6 (20 ng/mL), LIF (1:1000), or OSM (20 ng/mL) ( B-D ). Cells were serum-starved for 16 hours before the addition of recombinant proteins. B , Protein expression 1 hour after recombinant protein treatment. C , mRNA expression of CTGF 3 hours after recombinant protein treatment. D , WST-8 assay at the indicated time points after treatment with recombinant proteins. HepG2 cells and Alex cells were transfected with gp130 siRNA, STAT3 siRNA, or control siRNA 48 hours before the addition of recombinant proteins ( E-F ). Recombinant proteins were added 16 hours after serum starvation. E , mRNA expression of CTGF 3 hours after treatment with recombinant proteins. F , WST-8 assay at the indicated time points after recombinant protein treatment (n = 3-4). ∗ P < .05.

    Techniques Used: Expressing, Concentration Assay, Enzyme-linked Immunosorbent Assay, Recombinant, Transfection, Control

    Knockdown of CTGF in HepG2 cells decreased IL-6 family cytokine expression in stromal cells, downregulated p-STAT3 expression in HepG2 cells and reduced the proliferation of HepG2 cells. Western blotting of HepG2 or Alex cells treated with recombinant CTGF protein under monoculture ( A ). Protein lysate was collected from cells 0, 0.5, 1, and 3 hours after the addition of 5 nM recombinant CTGF protein. HepG2 cells were incubated under monoculture or coculture with stromal cell lines ( B-E ). HepG2 cells were transfected with CTGF siRNA or control siRNA 48 hours before coculturing. Total proteins and RNA were collected after 24 hours of coculture. THP-1 cells had been pretreated with 100 ng/m phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculture. B , Western blot showing HepG2 cell proteins in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells. C , WST-8 assay of HepG2 cells performed 48 hours after initiation of monoculture or coculture (n = 3). ∗ P < .05. D , mRNA expression of IL-6 family cytokines in stromal cell lines in monoculture or cocultured with HepG2 cells transfected with CTGF siRNA or control siRNA (n = 4). E , IL-6 concentration in supernatant measured via enzyme-linked immunosorbent assay (n = 4). ∗ P < .05 vs monoculture; ∗∗ P < .05 vs coculture with HepG2 control si.
    Figure Legend Snippet: Knockdown of CTGF in HepG2 cells decreased IL-6 family cytokine expression in stromal cells, downregulated p-STAT3 expression in HepG2 cells and reduced the proliferation of HepG2 cells. Western blotting of HepG2 or Alex cells treated with recombinant CTGF protein under monoculture ( A ). Protein lysate was collected from cells 0, 0.5, 1, and 3 hours after the addition of 5 nM recombinant CTGF protein. HepG2 cells were incubated under monoculture or coculture with stromal cell lines ( B-E ). HepG2 cells were transfected with CTGF siRNA or control siRNA 48 hours before coculturing. Total proteins and RNA were collected after 24 hours of coculture. THP-1 cells had been pretreated with 100 ng/m phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculture. B , Western blot showing HepG2 cell proteins in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells. C , WST-8 assay of HepG2 cells performed 48 hours after initiation of monoculture or coculture (n = 3). ∗ P < .05. D , mRNA expression of IL-6 family cytokines in stromal cell lines in monoculture or cocultured with HepG2 cells transfected with CTGF siRNA or control siRNA (n = 4). E , IL-6 concentration in supernatant measured via enzyme-linked immunosorbent assay (n = 4). ∗ P < .05 vs monoculture; ∗∗ P < .05 vs coculture with HepG2 control si.

    Techniques Used: Knockdown, Expressing, Western Blot, Recombinant, Incubation, Transfection, Control, Concentration Assay, Enzyme-linked Immunosorbent Assay



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    alex human hepatoma cell line  (JCRB Cell Bank)
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    JCRB Cell Bank alex human hepatoma cell line
    Stromal cells increased p-STAT3 and CTGF expression and cell growth in hepatoma <t>cells.</t> <t>HepG2</t> or <t>Alex</t> cells were transfected with STAT3 siRNA or control siRNA ( A-B ). WST-8 assay ( A ) and CTGF mRNA expression ( B ) of HepG2 or Alex cells after siRNA transfection. Total RNA was collected 48 hours after siRNA transfection. HepG2 or Alex cells were incubated in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells, using Transwell insert system ( C-G ). THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculturing. Total proteins and RNA were collected after 24 hours of incubation ( C, E, F ). C , Western blot showing protein expression of HepG2 or Alex cells. D , WST-8 assay of HepG2 or Alex cells in coculture at the indicated time points. HepG2 or Alex cells were transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours before coculturing ( E-G ). E , Western blot showing protein expression and qPCR showing CTGF mRNA expression in HepG2 or Alex cells transfected with STAT3 siRNA or control siRNA. F , Western blot and CTGF mRNA expression in HepG2 or Alex cells transfected with gp130 siRNA or control siRNA. G , WST-8 assay of HepG2 or Alex cells transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours after incubation (n = 3-4). ∗ , †, ‡, § P < .05 vs control.
    Alex Human Hepatoma Cell Line, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/alex human hepatoma cell line/product/JCRB Cell Bank
    Average 90 stars, based on 1 article reviews
    alex human hepatoma cell line - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Stromal cells increased p-STAT3 and CTGF expression and cell growth in hepatoma cells. HepG2 or Alex cells were transfected with STAT3 siRNA or control siRNA ( A-B ). WST-8 assay ( A ) and CTGF mRNA expression ( B ) of HepG2 or Alex cells after siRNA transfection. Total RNA was collected 48 hours after siRNA transfection. HepG2 or Alex cells were incubated in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells, using Transwell insert system ( C-G ). THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculturing. Total proteins and RNA were collected after 24 hours of incubation ( C, E, F ). C , Western blot showing protein expression of HepG2 or Alex cells. D , WST-8 assay of HepG2 or Alex cells in coculture at the indicated time points. HepG2 or Alex cells were transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours before coculturing ( E-G ). E , Western blot showing protein expression and qPCR showing CTGF mRNA expression in HepG2 or Alex cells transfected with STAT3 siRNA or control siRNA. F , Western blot and CTGF mRNA expression in HepG2 or Alex cells transfected with gp130 siRNA or control siRNA. G , WST-8 assay of HepG2 or Alex cells transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours after incubation (n = 3-4). ∗ , †, ‡, § P < .05 vs control.

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    Article Title: STAT3 is Activated by CTGF-mediated Tumor-stroma Cross Talk to Promote HCC Progression

    doi: 10.1016/j.jcmgh.2022.09.006

    Figure Lengend Snippet: Stromal cells increased p-STAT3 and CTGF expression and cell growth in hepatoma cells. HepG2 or Alex cells were transfected with STAT3 siRNA or control siRNA ( A-B ). WST-8 assay ( A ) and CTGF mRNA expression ( B ) of HepG2 or Alex cells after siRNA transfection. Total RNA was collected 48 hours after siRNA transfection. HepG2 or Alex cells were incubated in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells, using Transwell insert system ( C-G ). THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculturing. Total proteins and RNA were collected after 24 hours of incubation ( C, E, F ). C , Western blot showing protein expression of HepG2 or Alex cells. D , WST-8 assay of HepG2 or Alex cells in coculture at the indicated time points. HepG2 or Alex cells were transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours before coculturing ( E-G ). E , Western blot showing protein expression and qPCR showing CTGF mRNA expression in HepG2 or Alex cells transfected with STAT3 siRNA or control siRNA. F , Western blot and CTGF mRNA expression in HepG2 or Alex cells transfected with gp130 siRNA or control siRNA. G , WST-8 assay of HepG2 or Alex cells transfected with STAT3 siRNA, gp130 siRNA, or control siRNA 48 hours after incubation (n = 3-4). ∗ , †, ‡, § P < .05 vs control.

    Article Snippet: The HepG2 and Alex human hepatoma cell lines were obtained from the Japanese Collection of Research Bioresources/Health Science Research Resources Bank (JCRB/HSRRB) cell bank (Osaka, Japan) (JCRB Cat# NIHS0326, RRID:CVCL 0027 and JCRB Cat# JCRB0406, RRID:CVCL_0485, respectively).

    Techniques: Expressing, Transfection, Control, Incubation, Western Blot

    IL-6 family cytokines increased p-STAT3 and CTGF expression in hepatoma cells and enhanced cell proliferation. Concentrations of IL-6, LIF, and OSM in the culture supernatant ( A ). Culture supernatant was collected 24 hours after the initiation of HepG2, Alex, LX-2, THP-1, MTA, and TMNK-1 cell monoculture. IL-6, LIF, or OSM concentration was measured by enzyme-linked immunosorbent assay. THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation, and the culture medium was replaced with PMA-free medium 24 hours before supernatant collection. HepG2 cells and Alex cells were treated with recombinant proteins of IL-6 (20 ng/mL), LIF (1:1000), or OSM (20 ng/mL) ( B-D ). Cells were serum-starved for 16 hours before the addition of recombinant proteins. B , Protein expression 1 hour after recombinant protein treatment. C , mRNA expression of CTGF 3 hours after recombinant protein treatment. D , WST-8 assay at the indicated time points after treatment with recombinant proteins. HepG2 cells and Alex cells were transfected with gp130 siRNA, STAT3 siRNA, or control siRNA 48 hours before the addition of recombinant proteins ( E-F ). Recombinant proteins were added 16 hours after serum starvation. E , mRNA expression of CTGF 3 hours after treatment with recombinant proteins. F , WST-8 assay at the indicated time points after recombinant protein treatment (n = 3-4). ∗ P < .05.

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    Article Title: STAT3 is Activated by CTGF-mediated Tumor-stroma Cross Talk to Promote HCC Progression

    doi: 10.1016/j.jcmgh.2022.09.006

    Figure Lengend Snippet: IL-6 family cytokines increased p-STAT3 and CTGF expression in hepatoma cells and enhanced cell proliferation. Concentrations of IL-6, LIF, and OSM in the culture supernatant ( A ). Culture supernatant was collected 24 hours after the initiation of HepG2, Alex, LX-2, THP-1, MTA, and TMNK-1 cell monoculture. IL-6, LIF, or OSM concentration was measured by enzyme-linked immunosorbent assay. THP-1 cells were pretreated with 100 ng/mL phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation, and the culture medium was replaced with PMA-free medium 24 hours before supernatant collection. HepG2 cells and Alex cells were treated with recombinant proteins of IL-6 (20 ng/mL), LIF (1:1000), or OSM (20 ng/mL) ( B-D ). Cells were serum-starved for 16 hours before the addition of recombinant proteins. B , Protein expression 1 hour after recombinant protein treatment. C , mRNA expression of CTGF 3 hours after recombinant protein treatment. D , WST-8 assay at the indicated time points after treatment with recombinant proteins. HepG2 cells and Alex cells were transfected with gp130 siRNA, STAT3 siRNA, or control siRNA 48 hours before the addition of recombinant proteins ( E-F ). Recombinant proteins were added 16 hours after serum starvation. E , mRNA expression of CTGF 3 hours after treatment with recombinant proteins. F , WST-8 assay at the indicated time points after recombinant protein treatment (n = 3-4). ∗ P < .05.

    Article Snippet: The HepG2 and Alex human hepatoma cell lines were obtained from the Japanese Collection of Research Bioresources/Health Science Research Resources Bank (JCRB/HSRRB) cell bank (Osaka, Japan) (JCRB Cat# NIHS0326, RRID:CVCL 0027 and JCRB Cat# JCRB0406, RRID:CVCL_0485, respectively).

    Techniques: Expressing, Concentration Assay, Enzyme-linked Immunosorbent Assay, Recombinant, Transfection, Control

    Knockdown of CTGF in HepG2 cells decreased IL-6 family cytokine expression in stromal cells, downregulated p-STAT3 expression in HepG2 cells and reduced the proliferation of HepG2 cells. Western blotting of HepG2 or Alex cells treated with recombinant CTGF protein under monoculture ( A ). Protein lysate was collected from cells 0, 0.5, 1, and 3 hours after the addition of 5 nM recombinant CTGF protein. HepG2 cells were incubated under monoculture or coculture with stromal cell lines ( B-E ). HepG2 cells were transfected with CTGF siRNA or control siRNA 48 hours before coculturing. Total proteins and RNA were collected after 24 hours of coculture. THP-1 cells had been pretreated with 100 ng/m phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculture. B , Western blot showing HepG2 cell proteins in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells. C , WST-8 assay of HepG2 cells performed 48 hours after initiation of monoculture or coculture (n = 3). ∗ P < .05. D , mRNA expression of IL-6 family cytokines in stromal cell lines in monoculture or cocultured with HepG2 cells transfected with CTGF siRNA or control siRNA (n = 4). E , IL-6 concentration in supernatant measured via enzyme-linked immunosorbent assay (n = 4). ∗ P < .05 vs monoculture; ∗∗ P < .05 vs coculture with HepG2 control si.

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    Article Title: STAT3 is Activated by CTGF-mediated Tumor-stroma Cross Talk to Promote HCC Progression

    doi: 10.1016/j.jcmgh.2022.09.006

    Figure Lengend Snippet: Knockdown of CTGF in HepG2 cells decreased IL-6 family cytokine expression in stromal cells, downregulated p-STAT3 expression in HepG2 cells and reduced the proliferation of HepG2 cells. Western blotting of HepG2 or Alex cells treated with recombinant CTGF protein under monoculture ( A ). Protein lysate was collected from cells 0, 0.5, 1, and 3 hours after the addition of 5 nM recombinant CTGF protein. HepG2 cells were incubated under monoculture or coculture with stromal cell lines ( B-E ). HepG2 cells were transfected with CTGF siRNA or control siRNA 48 hours before coculturing. Total proteins and RNA were collected after 24 hours of coculture. THP-1 cells had been pretreated with 100 ng/m phorbol 12-myristate 13-acetate (PMA) for 48 hours to induce macrophage differentiation before coculture. B , Western blot showing HepG2 cell proteins in monoculture or cocultured with LX-2, THP-1, MTA, and TMNK-1 cells. C , WST-8 assay of HepG2 cells performed 48 hours after initiation of monoculture or coculture (n = 3). ∗ P < .05. D , mRNA expression of IL-6 family cytokines in stromal cell lines in monoculture or cocultured with HepG2 cells transfected with CTGF siRNA or control siRNA (n = 4). E , IL-6 concentration in supernatant measured via enzyme-linked immunosorbent assay (n = 4). ∗ P < .05 vs monoculture; ∗∗ P < .05 vs coculture with HepG2 control si.

    Article Snippet: The HepG2 and Alex human hepatoma cell lines were obtained from the Japanese Collection of Research Bioresources/Health Science Research Resources Bank (JCRB/HSRRB) cell bank (Osaka, Japan) (JCRB Cat# NIHS0326, RRID:CVCL 0027 and JCRB Cat# JCRB0406, RRID:CVCL_0485, respectively).

    Techniques: Knockdown, Expressing, Western Blot, Recombinant, Incubation, Transfection, Control, Concentration Assay, Enzyme-linked Immunosorbent Assay