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pcmv ha mammalian expression vector  (TaKaRa)


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    TaKaRa pcmv ha mammalian expression vector
    Pcmv Ha Mammalian Expression Vector, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 770 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pcmv+ha+expression+vector/pCMV-HA+Vector+Set/bio_rxiv__2025__08__02__668297-212-1-15
    Average 96 stars, based on 770 article reviews
    pcmv ha mammalian expression vector - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Expressing:

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [ , ], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see ). ..

    Article Title: MEF2B instructs germinal center development and acts as an oncogene in B cell lymphomagenesis
    Article Snippet: The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HDAC9 coding sequence (GeneBank accession number {"type":"entrez-nucleotide","attrs":{"text":"NM_178425.3","term_id":"1013400628"}} NM_178425.3 ) was amplified by PCR from cDNA of human GC B cells and was subcloned into the pCMV-FLAG expression vector (Stratagene).

    Article Title: Characterization of clinical envelopes with lack of sensitivity to the HIV-1 inhibitors temsavir and ibalizumab.
    Article Snippet: .. Products from the secondary PCR were cloned into the pCMV-HA expression vector (Takara Bio Inc) using Nonbuilder® HiFi DNA Assembly Master Mix (New England Biolabs, Ipswich, MA), sequenced, and designated BRIGHTE_A_BL1-4. ..

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases.
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [4,34], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see subsection 2.4.3). ..

    Article Title: Transmembrane protein 168 mutation reduces cardiomyocyte cell surface expression of Nav1.5 through αB-crystallin intracellular dynamics.
    Article Snippet: Transmembrane protein 168 (TMEM168) was found to be localized on the nuclear membrane.. A heterozygous mutation (c.1616G>A, p. R539Q) in TMEM168 was identified in patients with Brugada syndrome.. This mutation reduced expression of cardiomyocyte sodium channel Nav1.5 via Nedd4-2 E3 ubiquitin ligase-induced ubiquitination and degradation.

    Article Title: Discovery and Characterization of a Novel CD4-Binding Adnectin with Potent Anti-HIV Activity
    Article Snippet: .. The envelope genes were cloned into the pCMV-HA expression vector (Clontech) using the In-Fusion HD EcoDry technology (Clontech) and were used in the assay to evaluate a wide spectrum of subtypes. ..

    Article Title: E3 ligase Nedd4l promotes antiviral innate immunity by catalyzing K29-linked cysteine ubiquitination of TRAF3
    Article Snippet: The plasmid expressing Nedd4l was obtained from Origene. .. TRAF3 and TBK1 were amplified from mRNA of Hela cells and RAW264.7, respectively, by reverse transcription-PCR and the cDNA expressing full-length TRAF3 or TBK1 were cloned into pcDNA3.1-Flag, pCMV-Myc, or pCMV-HA expression vector (Clontech) to construct Flag-, Myc-, or HA-tagged TRAF3 and TBK1-expressing plasmids , . .. Mutant Nedd4l and TRAF3 plasmids were constructed using Takara MutanBEST kit (R401) according to the manufacturer’s instructions.

    Plasmid Preparation:

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [ , ], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see ). ..

    Article Title: MEF2B instructs germinal center development and acts as an oncogene in B cell lymphomagenesis
    Article Snippet: The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HDAC9 coding sequence (GeneBank accession number {"type":"entrez-nucleotide","attrs":{"text":"NM_178425.3","term_id":"1013400628"}} NM_178425.3 ) was amplified by PCR from cDNA of human GC B cells and was subcloned into the pCMV-FLAG expression vector (Stratagene).

    Article Title: Characterization of clinical envelopes with lack of sensitivity to the HIV-1 inhibitors temsavir and ibalizumab.
    Article Snippet: .. Products from the secondary PCR were cloned into the pCMV-HA expression vector (Takara Bio Inc) using Nonbuilder® HiFi DNA Assembly Master Mix (New England Biolabs, Ipswich, MA), sequenced, and designated BRIGHTE_A_BL1-4. ..

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases.
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [4,34], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see subsection 2.4.3). ..

    Article Title: Transmembrane protein 168 mutation reduces cardiomyocyte cell surface expression of Nav1.5 through αB-crystallin intracellular dynamics.
    Article Snippet: Transmembrane protein 168 (TMEM168) was found to be localized on the nuclear membrane.. A heterozygous mutation (c.1616G>A, p. R539Q) in TMEM168 was identified in patients with Brugada syndrome.. This mutation reduced expression of cardiomyocyte sodium channel Nav1.5 via Nedd4-2 E3 ubiquitin ligase-induced ubiquitination and degradation.

    Article Title: Discovery and Characterization of a Novel CD4-Binding Adnectin with Potent Anti-HIV Activity
    Article Snippet: .. The envelope genes were cloned into the pCMV-HA expression vector (Clontech) using the In-Fusion HD EcoDry technology (Clontech) and were used in the assay to evaluate a wide spectrum of subtypes. ..

    Article Title: E3 ligase Nedd4l promotes antiviral innate immunity by catalyzing K29-linked cysteine ubiquitination of TRAF3
    Article Snippet: The plasmid expressing Nedd4l was obtained from Origene. .. TRAF3 and TBK1 were amplified from mRNA of Hela cells and RAW264.7, respectively, by reverse transcription-PCR and the cDNA expressing full-length TRAF3 or TBK1 were cloned into pcDNA3.1-Flag, pCMV-Myc, or pCMV-HA expression vector (Clontech) to construct Flag-, Myc-, or HA-tagged TRAF3 and TBK1-expressing plasmids , . .. Mutant Nedd4l and TRAF3 plasmids were constructed using Takara MutanBEST kit (R401) according to the manufacturer’s instructions.

    Clone Assay:

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [ , ], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see ). ..

    Article Title: Characterization of clinical envelopes with lack of sensitivity to the HIV-1 inhibitors temsavir and ibalizumab.
    Article Snippet: .. Products from the secondary PCR were cloned into the pCMV-HA expression vector (Takara Bio Inc) using Nonbuilder® HiFi DNA Assembly Master Mix (New England Biolabs, Ipswich, MA), sequenced, and designated BRIGHTE_A_BL1-4. ..

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases.
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [4,34], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see subsection 2.4.3). ..

    Article Title: Discovery and Characterization of a Novel CD4-Binding Adnectin with Potent Anti-HIV Activity
    Article Snippet: .. The envelope genes were cloned into the pCMV-HA expression vector (Clontech) using the In-Fusion HD EcoDry technology (Clontech) and were used in the assay to evaluate a wide spectrum of subtypes. ..

    Article Title: E3 ligase Nedd4l promotes antiviral innate immunity by catalyzing K29-linked cysteine ubiquitination of TRAF3
    Article Snippet: The plasmid expressing Nedd4l was obtained from Origene. .. TRAF3 and TBK1 were amplified from mRNA of Hela cells and RAW264.7, respectively, by reverse transcription-PCR and the cDNA expressing full-length TRAF3 or TBK1 were cloned into pcDNA3.1-Flag, pCMV-Myc, or pCMV-HA expression vector (Clontech) to construct Flag-, Myc-, or HA-tagged TRAF3 and TBK1-expressing plasmids , . .. Mutant Nedd4l and TRAF3 plasmids were constructed using Takara MutanBEST kit (R401) according to the manufacturer’s instructions.

    Transfection:

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [ , ], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see ). ..

    Article Title: Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases.
    Article Snippet: Regarding the secondary antibodies, horseradish peroxidase (HRP)-linked horse anti-mouse immunoglobulin G (IgG; Cell Signaling Technology (7076); 0.015 μg/mL) and HRP-linked goat anti-rabbit IgG (Cell Signaling Technology (7074); 0.007 μg/mL) were used for immunoblotting, whereas Alexa Fluor 488-conjugated goat anti-rabbit IgG (Invitrogen (A-11008); 6.67 μg/mL) and Alexa Fluor 594-conjugated goat anti-mouse IgG (Invitrogen (A-11005); 6.67 μg/mL) were utilized for immunocytochemistry. .. Human full-length LAP1B complementary DNA (cDNA) cloned into the pCMV-Myc expression vector (Clontech, Takara Bio USA, San Jose, California, USA) and human full-length LAP1C cDNA cloned into the pCMV-HA expression vector (Clontech), prepared as previously described by Santos et al. [4,34], were used in cell transfections to express Myc-LAP1B and HA-LAP1C fusion proteins, respectively (see subsection 2.4.3). ..

    Sequencing:

    Article Title: MEF2B instructs germinal center development and acts as an oncogene in B cell lymphomagenesis
    Article Snippet: The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HDAC9 coding sequence (GeneBank accession number {"type":"entrez-nucleotide","attrs":{"text":"NM_178425.3","term_id":"1013400628"}} NM_178425.3 ) was amplified by PCR from cDNA of human GC B cells and was subcloned into the pCMV-FLAG expression vector (Stratagene).

    Amplification:

    Article Title: MEF2B instructs germinal center development and acts as an oncogene in B cell lymphomagenesis
    Article Snippet: The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HDAC9 coding sequence (GeneBank accession number {"type":"entrez-nucleotide","attrs":{"text":"NM_178425.3","term_id":"1013400628"}} NM_178425.3 ) was amplified by PCR from cDNA of human GC B cells and was subcloned into the pCMV-FLAG expression vector (Stratagene).

    Article Title: Transmembrane protein 168 mutation reduces cardiomyocyte cell surface expression of Nav1.5 through αB-crystallin intracellular dynamics.
    Article Snippet: Transmembrane protein 168 (TMEM168) was found to be localized on the nuclear membrane.. A heterozygous mutation (c.1616G>A, p. R539Q) in TMEM168 was identified in patients with Brugada syndrome.. This mutation reduced expression of cardiomyocyte sodium channel Nav1.5 via Nedd4-2 E3 ubiquitin ligase-induced ubiquitination and degradation.

    Article Title: E3 ligase Nedd4l promotes antiviral innate immunity by catalyzing K29-linked cysteine ubiquitination of TRAF3
    Article Snippet: The plasmid expressing Nedd4l was obtained from Origene. .. TRAF3 and TBK1 were amplified from mRNA of Hela cells and RAW264.7, respectively, by reverse transcription-PCR and the cDNA expressing full-length TRAF3 or TBK1 were cloned into pcDNA3.1-Flag, pCMV-Myc, or pCMV-HA expression vector (Clontech) to construct Flag-, Myc-, or HA-tagged TRAF3 and TBK1-expressing plasmids , . .. Mutant Nedd4l and TRAF3 plasmids were constructed using Takara MutanBEST kit (R401) according to the manufacturer’s instructions.

    Polymerase Chain Reaction:

    Article Title: MEF2B instructs germinal center development and acts as an oncogene in B cell lymphomagenesis
    Article Snippet: The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HIRA (GeneBank accession number NM_003325.3) and ASF1a (GeneBank accession number NM_014034.2) coding sequence were amplified by PCR from cDNA of human GC B cells and subcloned into pCMV-HA expression vector (Clontech). .. The HDAC9 coding sequence (GeneBank accession number {"type":"entrez-nucleotide","attrs":{"text":"NM_178425.3","term_id":"1013400628"}} NM_178425.3 ) was amplified by PCR from cDNA of human GC B cells and was subcloned into the pCMV-FLAG expression vector (Stratagene).

    Article Title: Characterization of clinical envelopes with lack of sensitivity to the HIV-1 inhibitors temsavir and ibalizumab.
    Article Snippet: .. Products from the secondary PCR were cloned into the pCMV-HA expression vector (Takara Bio Inc) using Nonbuilder® HiFi DNA Assembly Master Mix (New England Biolabs, Ipswich, MA), sequenced, and designated BRIGHTE_A_BL1-4. ..

    Article Title: Transmembrane protein 168 mutation reduces cardiomyocyte cell surface expression of Nav1.5 through αB-crystallin intracellular dynamics.
    Article Snippet: Transmembrane protein 168 (TMEM168) was found to be localized on the nuclear membrane.. A heterozygous mutation (c.1616G>A, p. R539Q) in TMEM168 was identified in patients with Brugada syndrome.. This mutation reduced expression of cardiomyocyte sodium channel Nav1.5 via Nedd4-2 E3 ubiquitin ligase-induced ubiquitination and degradation.

    Construct:

    Article Title: E3 ligase Nedd4l promotes antiviral innate immunity by catalyzing K29-linked cysteine ubiquitination of TRAF3
    Article Snippet: The plasmid expressing Nedd4l was obtained from Origene. .. TRAF3 and TBK1 were amplified from mRNA of Hela cells and RAW264.7, respectively, by reverse transcription-PCR and the cDNA expressing full-length TRAF3 or TBK1 were cloned into pcDNA3.1-Flag, pCMV-Myc, or pCMV-HA expression vector (Clontech) to construct Flag-, Myc-, or HA-tagged TRAF3 and TBK1-expressing plasmids , . .. Mutant Nedd4l and TRAF3 plasmids were constructed using Takara MutanBEST kit (R401) according to the manufacturer’s instructions.



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