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profinity exacttm protein purification systems  (Bio-Rad)


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    Bio-Rad profinity exacttm protein purification systems
    UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the <t>Profinity</t> eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated <t>purification</t> steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .
    Profinity Exacttm Protein Purification Systems, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 78 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/profinity exacttm protein purification systems/product/Bio-Rad
    Average 93 stars, based on 78 article reviews
    profinity exacttm protein purification systems - by Bioz Stars, 2026-04
    93/100 stars

    Images

    1) Product Images from "Activation of hepatic stellate cells by the ubiquitin C-terminal hydrolase 1 protein secreted from hepatitis C virus-infected hepatocytes"

    Article Title: Activation of hepatic stellate cells by the ubiquitin C-terminal hydrolase 1 protein secreted from hepatitis C virus-infected hepatocytes

    Journal: Scientific Reports

    doi: 10.1038/s41598-017-04259-7

    UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the Profinity eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated purification steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .
    Figure Legend Snippet: UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the Profinity eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated purification steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .

    Techniques Used: Activation Assay, Cell Culture, Control, Expressing, Western Blot, Positive Control, Recombinant, Purification, SDS Page, Staining, Molecular Weight, Protein Purification



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    profinity exacttm protein purification systems  (Bio-Rad)
    93
    Bio-Rad profinity exacttm protein purification systems
    UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the <t>Profinity</t> eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated <t>purification</t> steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .
    Profinity Exacttm Protein Purification Systems, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/profinity exacttm protein purification systems/product/Bio-Rad
    Average 93 stars, based on 1 article reviews
    profinity exacttm protein purification systems - by Bioz Stars, 2026-04
    93/100 stars
    		  Buy from Supplier
    profinity exacttm protein purification system  (Bio-Rad)
    90
    Bio-Rad profinity exacttm protein purification system
    UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the <t>Profinity</t> eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated <t>purification</t> steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .
    Profinity Exacttm Protein Purification System, supplied by Bio-Rad, 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/profinity exacttm protein purification system/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    profinity exacttm protein purification system - by Bioz Stars, 2026-04
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the Profinity eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated purification steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .

    Journal: Scientific Reports

    Article Title: Activation of hepatic stellate cells by the ubiquitin C-terminal hydrolase 1 protein secreted from hepatitis C virus-infected hepatocytes

    doi: 10.1038/s41598-017-04259-7

    Figure Lengend Snippet: UCHL1 induced HSCs activation. ( A ) HSC-T6 cells (1 × 10 6 cells) were co-cultured with Con1 or Huh7 cells (1 × 10 5 cells) in the presence or absence of anti-UCHL1 antibody or mouse IgG control antibody for 24 h. The HSC-T6 cell lysate was collected and the expression of α-SMA was determined by Western blot analysis. HSC-T6 cells treated with DMEM and TGF-β1 were used as the negative and positive control of HSC activation, respectively. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. ( B ) Recombinant UCHL1 protein fused to the Profinity eXact tag was expressed in E . coli BL21 after IPTG induction. Samples from the indicated purification steps were fractionated on a 12% SDS-PAGE and stained with Coomassie Brilliant Blue (upper panel). The protein with an expected molecular weight of UCHL1 (21 kDa) was noted in the eluted fraction after protease cleavage of the Profinity eXact tag and was indicated as *. The recombinant UCHL1 protein in the indicated steps of protein purification was further confirmed by Western blotting using the anti-UCHL1 antibody (lower panel). The cell lysate of Con1 was used as a positive control. ( C ) HSC-T6 cells were culture in DMEM w/o FBS for 24 h and then treated with the indicated concentrations of purified rUCHL1 or BSA for an additional 24 h. The cell lysates were collected and the expression of α-SMA was determined by Western blot analysis. The expression of β-tubulin was used as the control for equal protein loading. The number below the gel images represents the relatively α-SMA expression levels for the indicated experimental condition after normalization with the expression of β-tubulin. HSCs treated with DMEM and TGFβ1 (10 ng/ml) were used as negative and positive controls for HSC stimulation, respectively. The full Western blot and the corresponding positions of the molecular weight protein markers are presented in Supplementary Fig. .

    Article Snippet: The supernatant rUCHL1 protein was purified by using the Profinity eXactTM Protein Purification Systems (Bio-Rad, Richmond, CA) and was concentrated using an Amicon Ultra-4 ® 10 K (Millipore, Bedford, MA) for further analysis.

    Techniques: Activation Assay, Cell Culture, Control, Expressing, Western Blot, Positive Control, Recombinant, Purification, SDS Page, Staining, Molecular Weight, Protein Purification