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soluble fusion protein gpc3  (TaKaRa)


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    Structured Review

    TaKaRa soluble fusion protein gpc3
    Figure 3. Expression, purification and identification of recombinant <t>GPC3</t> protein. (A) Induction expression of recombinant GPC3 protein by SDS‑PAGE analysis. Lane M, protein molecular weight marker; Lane 1, non‑induction of GPC3; lane 2, induction of GPC3. (B) SDS‑PAGE analysis of purification of recombinant GPC3 protein. M, standard protein molecular weight; lane 1, purified protein. (C) Confirmation of the recombinant protein by western blot analysis. The primary antibody was rabbit anti‑His‑tag monoclonal antibody. M, standard protein molecular weight; lane 1, purified protein. GPC3, glypican‑3.
    Soluble Fusion Protein Gpc3, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 512 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/soluble+fusion+protein+gpc3/Protein+Molecular+Weight+Marker/pm30896845-57-15-27
    Average 94 stars, based on 512 article reviews
    soluble fusion protein gpc3 - by Bioz Stars, 2026-10
    94/100 stars

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    1) Product Images from "Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3."

    Article Title: Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3.

    Journal: Molecular medicine reports

    doi: 10.3892/mmr.2019.10019

    Figure 3. Expression, purification and identification of recombinant GPC3 protein. (A) Induction expression of recombinant GPC3 protein by SDS‑PAGE analysis. Lane M, protein molecular weight marker; Lane 1, non‑induction of GPC3; lane 2, induction of GPC3. (B) SDS‑PAGE analysis of purification of recombinant GPC3 protein. M, standard protein molecular weight; lane 1, purified protein. (C) Confirmation of the recombinant protein by western blot analysis. The primary antibody was rabbit anti‑His‑tag monoclonal antibody. M, standard protein molecular weight; lane 1, purified protein. GPC3, glypican‑3.
    Figure Legend Snippet: Figure 3. Expression, purification and identification of recombinant GPC3 protein. (A) Induction expression of recombinant GPC3 protein by SDS‑PAGE analysis. Lane M, protein molecular weight marker; Lane 1, non‑induction of GPC3; lane 2, induction of GPC3. (B) SDS‑PAGE analysis of purification of recombinant GPC3 protein. M, standard protein molecular weight; lane 1, purified protein. (C) Confirmation of the recombinant protein by western blot analysis. The primary antibody was rabbit anti‑His‑tag monoclonal antibody. M, standard protein molecular weight; lane 1, purified protein. GPC3, glypican‑3.

    Techniques Used: Expressing, Purification, Recombinant, Molecular Weight, Marker, Western Blot

    Related Articles

    Recombinant:

    Article Title: Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3.
    Article Snippet: PCR fragments were digested using BamHI and XhoI restriction enzymes (10 U/μl; Takara Bio, Inc.) for 1 h at 37 ̊C and then cloned into the BamHI- and XhoI-digested pET16b vector ecoding a His‐tag (Novagen; Merck KGaA); successful cloning was confirmed by sequencing (Sangon Biotech Co., Ltd.). .. The recombinant plasmid was transfected into E. coli BL21 (DE3, Novagen; Merck KGaA) with the soluble fusion protein GPC3 expressed following induction with 0.1 mM isopropyl-β-Dthiogalactopyranoside (IPTG; Takara Bio, Inc.), and non-IPTG cells were used as control. ..

    Plasmid Preparation:

    Article Title: Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3.
    Article Snippet: PCR fragments were digested using BamHI and XhoI restriction enzymes (10 U/μl; Takara Bio, Inc.) for 1 h at 37 ̊C and then cloned into the BamHI- and XhoI-digested pET16b vector ecoding a His‐tag (Novagen; Merck KGaA); successful cloning was confirmed by sequencing (Sangon Biotech Co., Ltd.). .. The recombinant plasmid was transfected into E. coli BL21 (DE3, Novagen; Merck KGaA) with the soluble fusion protein GPC3 expressed following induction with 0.1 mM isopropyl-β-Dthiogalactopyranoside (IPTG; Takara Bio, Inc.), and non-IPTG cells were used as control. ..

    Transfection:

    Article Title: Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3.
    Article Snippet: PCR fragments were digested using BamHI and XhoI restriction enzymes (10 U/μl; Takara Bio, Inc.) for 1 h at 37 ̊C and then cloned into the BamHI- and XhoI-digested pET16b vector ecoding a His‐tag (Novagen; Merck KGaA); successful cloning was confirmed by sequencing (Sangon Biotech Co., Ltd.). .. The recombinant plasmid was transfected into E. coli BL21 (DE3, Novagen; Merck KGaA) with the soluble fusion protein GPC3 expressed following induction with 0.1 mM isopropyl-β-Dthiogalactopyranoside (IPTG; Takara Bio, Inc.), and non-IPTG cells were used as control. ..

    Control:

    Article Title: Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3.
    Article Snippet: PCR fragments were digested using BamHI and XhoI restriction enzymes (10 U/μl; Takara Bio, Inc.) for 1 h at 37 ̊C and then cloned into the BamHI- and XhoI-digested pET16b vector ecoding a His‐tag (Novagen; Merck KGaA); successful cloning was confirmed by sequencing (Sangon Biotech Co., Ltd.). .. The recombinant plasmid was transfected into E. coli BL21 (DE3, Novagen; Merck KGaA) with the soluble fusion protein GPC3 expressed following induction with 0.1 mM isopropyl-β-Dthiogalactopyranoside (IPTG; Takara Bio, Inc.), and non-IPTG cells were used as control. ..



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    TaKaRa soluble fusion protein gpc3
    Figure 3. Expression, purification and identification of recombinant <t>GPC3</t> protein. (A) Induction expression of recombinant GPC3 protein by SDS‑PAGE analysis. Lane M, protein molecular weight marker; Lane 1, non‑induction of GPC3; lane 2, induction of GPC3. (B) SDS‑PAGE analysis of purification of recombinant GPC3 protein. M, standard protein molecular weight; lane 1, purified protein. (C) Confirmation of the recombinant protein by western blot analysis. The primary antibody was rabbit anti‑His‑tag monoclonal antibody. M, standard protein molecular weight; lane 1, purified protein. GPC3, glypican‑3.
    Soluble Fusion Protein Gpc3, supplied by TaKaRa, 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/product/soluble+fusion+protein+gpc3/Protein+Molecular+Weight+Marker/pm30896845-57-15-27
    Average 94 stars, based on 1 article reviews
    soluble fusion protein gpc3 - by Bioz Stars, 2026-10
    94/100 stars
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    Figure 3. Expression, purification and identification of recombinant GPC3 protein. (A) Induction expression of recombinant GPC3 protein by SDS‑PAGE analysis. Lane M, protein molecular weight marker; Lane 1, non‑induction of GPC3; lane 2, induction of GPC3. (B) SDS‑PAGE analysis of purification of recombinant GPC3 protein. M, standard protein molecular weight; lane 1, purified protein. (C) Confirmation of the recombinant protein by western blot analysis. The primary antibody was rabbit anti‑His‑tag monoclonal antibody. M, standard protein molecular weight; lane 1, purified protein. GPC3, glypican‑3.

    Journal: Molecular medicine reports

    Article Title: Preparation of a monoclonal antibody against the carcinoembryonic antigen, glypican‑3.

    doi: 10.3892/mmr.2019.10019

    Figure Lengend Snippet: Figure 3. Expression, purification and identification of recombinant GPC3 protein. (A) Induction expression of recombinant GPC3 protein by SDS‑PAGE analysis. Lane M, protein molecular weight marker; Lane 1, non‑induction of GPC3; lane 2, induction of GPC3. (B) SDS‑PAGE analysis of purification of recombinant GPC3 protein. M, standard protein molecular weight; lane 1, purified protein. (C) Confirmation of the recombinant protein by western blot analysis. The primary antibody was rabbit anti‑His‑tag monoclonal antibody. M, standard protein molecular weight; lane 1, purified protein. GPC3, glypican‑3.

    Article Snippet: The recombinant plasmid was transfected into E. coli BL21 (DE3, Novagen; Merck KGaA) with the soluble fusion protein GPC3 expressed following induction with 0.1 mM isopropyl-β-Dthiogalactopyranoside (IPTG; Takara Bio, Inc.), and non-IPTG cells were used as control.

    Techniques: Expressing, Purification, Recombinant, Molecular Weight, Marker, Western Blot