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h19-pflag-cmv-2 expression vector  (Millipore)


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    Structured Review

    Millipore h19-pflag-cmv-2 expression vector
    The sequence of the primers used for gene expression analysis
    H19 Pflag Cmv 2 Expression Vector, supplied by Millipore, 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/product/pflag-cmv-2+vectors/pflag+cmv2/pmc11299361-54-10-16
    Average 90 stars, based on 1 article reviews
    h19-pflag-cmv-2 expression vector - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Regulatory role of lncH19 in RAC1 alternative splicing: implication for RAC1B expression in colorectal cancer"

    Article Title: Regulatory role of lncH19 in RAC1 alternative splicing: implication for RAC1B expression in colorectal cancer

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    doi: 10.1186/s13046-024-03139-z

    The sequence of the primers used for gene expression analysis
    Figure Legend Snippet: The sequence of the primers used for gene expression analysis

    Techniques Used: Sequencing, Expressing

    The sequence of the biotin-labeled  H19  probes used for RNA pull-down assays
    Figure Legend Snippet: The sequence of the biotin-labeled H19 probes used for RNA pull-down assays

    Techniques Used: Sequencing

    RBFOX2 is involved in RAC1 alternative splicing in CRC cells. ( A - B - D , E - F - H ) QRT-PCR for the indicated mRNA in CRC cells, silenced for RBFOX2 with two different siRNA. Graphs show 2-ΔΔct calculated in silenced cells respect to relative controls (Normality test and t-test). ( C , F ) Western Blot and densitometric analyses for RAC1B in SW620 and HCT116 silenced for RBFOX2 and relative controls. For densitometric analysis data are represented as normalized OD. ( I - L ) qRT-PCR of the indicated genes in SW620 and HCT116 silenced for H19, the graphs represent the 2^- ΔΔ ct of the indicated calculated respect the expression in control cells. ( M ) Western Blot of RAC1b protein levels in CRC cells (SW620 and HCT116) in H19 silenced cells and relative control cells. Statistical analyses were performed using normality test and t-test, p-value is shown in th e graphs
    Figure Legend Snippet: RBFOX2 is involved in RAC1 alternative splicing in CRC cells. ( A - B - D , E - F - H ) QRT-PCR for the indicated mRNA in CRC cells, silenced for RBFOX2 with two different siRNA. Graphs show 2-ΔΔct calculated in silenced cells respect to relative controls (Normality test and t-test). ( C , F ) Western Blot and densitometric analyses for RAC1B in SW620 and HCT116 silenced for RBFOX2 and relative controls. For densitometric analysis data are represented as normalized OD. ( I - L ) qRT-PCR of the indicated genes in SW620 and HCT116 silenced for H19, the graphs represent the 2^- ΔΔ ct of the indicated calculated respect the expression in control cells. ( M ) Western Blot of RAC1b protein levels in CRC cells (SW620 and HCT116) in H19 silenced cells and relative control cells. Statistical analyses were performed using normality test and t-test, p-value is shown in th e graphs

    Techniques Used: Alternative Splicing, Quantitative RT-PCR, Western Blot, Expressing, Control

    Overexpression of lncH19 upregulates RAC1B expression. ( A ) qRT-PCR to analyze H19 mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( B ) qRT-PCR to analyze RAC1B mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( C ) Western Blot for RAC1B in CRC cells (SW620 and HCT116), transfected with lncH19 or empty vector. lncH19 overexpression promotes RAC1B nuclear localization. ( D ) Representative confocal microscopy images of anti-RAC1b immunofluorescence showed nuclear localization of RAC1b in lncH19-overexpressing CRC cells, SW620 (upper panel) and HCT116 (lower panel). The analysis of the RAC1B nuclear signal is reported on the histogram. ( E ) Western blot analysis and densitometric analyses for RAC1B in nuclear protein fractions of CRC cells (SW620 and HCT116) overexpressing H19 cells and relative control cells. E-F) Overexpression of lncH19 upregulate CiclinD and c-Myc expression through RAC1B activity qRT-PCR for the indicated genes in SW620 ( F ) and HCT116 ( G ) transfected with pH19 or empty vector and treated or not with RAC1B inhibitor. Statistical analyses were performed using: normality test, one sample t-test to compare different conditions to pEmpty untreated cells, and Two-tails unpaired t-test to compare two groups *; p-value is shown in the graphs
    Figure Legend Snippet: Overexpression of lncH19 upregulates RAC1B expression. ( A ) qRT-PCR to analyze H19 mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( B ) qRT-PCR to analyze RAC1B mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( C ) Western Blot for RAC1B in CRC cells (SW620 and HCT116), transfected with lncH19 or empty vector. lncH19 overexpression promotes RAC1B nuclear localization. ( D ) Representative confocal microscopy images of anti-RAC1b immunofluorescence showed nuclear localization of RAC1b in lncH19-overexpressing CRC cells, SW620 (upper panel) and HCT116 (lower panel). The analysis of the RAC1B nuclear signal is reported on the histogram. ( E ) Western blot analysis and densitometric analyses for RAC1B in nuclear protein fractions of CRC cells (SW620 and HCT116) overexpressing H19 cells and relative control cells. E-F) Overexpression of lncH19 upregulate CiclinD and c-Myc expression through RAC1B activity qRT-PCR for the indicated genes in SW620 ( F ) and HCT116 ( G ) transfected with pH19 or empty vector and treated or not with RAC1B inhibitor. Statistical analyses were performed using: normality test, one sample t-test to compare different conditions to pEmpty untreated cells, and Two-tails unpaired t-test to compare two groups *; p-value is shown in the graphs

    Techniques Used: Over Expression, Expressing, Quantitative RT-PCR, Transfection, Plasmid Preparation, Western Blot, Confocal Microscopy, Immunofluorescence, Control, Activity Assay

    Related Articles

    Mutagenesis:

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells.
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 Negatively Regulate the Cross-Talk between the PI3K/AKT Pathway and PPP Metabolism
    Article Snippet: Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Article Title: H19/let‑7/Lin28 ceRNA network mediates autophagy inhibiting epithelial‑mesenchymal transition in breast cancer.
    Article Snippet: Plasmids. pH19 and its corresponding mutant plasmid (pH19mut) were synthesized as previously described (18), with the 2.6‐kb‐long amplified H19 sequences inserted into pFLAG-CMV-2 vectors (Sigma-Aldrich; Merck KGaA).

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 negatively regulate the crosstalk between the PI3K/AKT pathway and PPP metabolism
    Article Snippet: The Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Plasmid Preparation:

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells.
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 Negatively Regulate the Cross-Talk between the PI3K/AKT Pathway and PPP Metabolism
    Article Snippet: Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Article Title: H19/let‑7/Lin28 ceRNA network mediates autophagy inhibiting epithelial‑mesenchymal transition in breast cancer.
    Article Snippet: Plasmids. pH19 and its corresponding mutant plasmid (pH19mut) were synthesized as previously described (18), with the 2.6‐kb‐long amplified H19 sequences inserted into pFLAG-CMV-2 vectors (Sigma-Aldrich; Merck KGaA).

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 negatively regulate the crosstalk between the PI3K/AKT pathway and PPP metabolism
    Article Snippet: The Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Synthesized:

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells.
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 Negatively Regulate the Cross-Talk between the PI3K/AKT Pathway and PPP Metabolism
    Article Snippet: Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Article Title: H19/let‑7/Lin28 ceRNA network mediates autophagy inhibiting epithelial‑mesenchymal transition in breast cancer.
    Article Snippet: Plasmids. pH19 and its corresponding mutant plasmid (pH19mut) were synthesized as previously described (18), with the 2.6‐kb‐long amplified H19 sequences inserted into pFLAG-CMV-2 vectors (Sigma-Aldrich; Merck KGaA).

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 negatively regulate the crosstalk between the PI3K/AKT pathway and PPP metabolism
    Article Snippet: The Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Amplification:

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells.
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 Negatively Regulate the Cross-Talk between the PI3K/AKT Pathway and PPP Metabolism
    Article Snippet: Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Article Title: H19/let‑7/Lin28 ceRNA network mediates autophagy inhibiting epithelial‑mesenchymal transition in breast cancer.
    Article Snippet: Plasmids. pH19 and its corresponding mutant plasmid (pH19mut) were synthesized as previously described (18), with the 2.6‐kb‐long amplified H19 sequences inserted into pFLAG-CMV-2 vectors (Sigma-Aldrich; Merck KGaA).

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 negatively regulate the crosstalk between the PI3K/AKT pathway and PPP metabolism
    Article Snippet: The Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Construct:

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells.
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 Negatively Regulate the Cross-Talk between the PI3K/AKT Pathway and PPP Metabolism
    Article Snippet: Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Article Title: H19/let‑7/Lin28 ceRNA network mediates autophagy inhibiting epithelial‑mesenchymal transition in breast cancer.
    Article Snippet: Plasmids. pH19 and its corresponding mutant plasmid (pH19mut) were synthesized as previously described (18), with the 2.6‐kb‐long amplified H19 sequences inserted into pFLAG-CMV-2 vectors (Sigma-Aldrich; Merck KGaA).

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 negatively regulate the crosstalk between the PI3K/AKT pathway and PPP metabolism
    Article Snippet: The Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Clone Assay:

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells.
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 Negatively Regulate the Cross-Talk between the PI3K/AKT Pathway and PPP Metabolism
    Article Snippet: Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).

    Article Title: H19/let‑7/Lin28 ceRNA network mediates autophagy inhibiting epithelial‑mesenchymal transition in breast cancer.
    Article Snippet: Plasmids. pH19 and its corresponding mutant plasmid (pH19mut) were synthesized as previously described (18), with the 2.6‐kb‐long amplified H19 sequences inserted into pFLAG-CMV-2 vectors (Sigma-Aldrich; Merck KGaA).

    Article Title: circRNA-SFMBT2 orchestrates ERα activation to drive tamoxifen resistance in breast cancer cells
    Article Snippet: Coding sequences of full-length ERα and its truncated proteins were cloned into pFLAG-CMV-2 vectors (Sigma, MO, USA) expressed a fused protein with an N-terminal Flag.

    Article Title: TRIM21 and PHLDA3 negatively regulate the crosstalk between the PI3K/AKT pathway and PPP metabolism
    Article Snippet: The Flag-PHLDA3 vectors were constructed by cloning PHLDA3 cDNA into the pFLAG-CMV-2 vectors (Sigma).



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    Image Search Results


    The sequence of the primers used for gene expression analysis

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: Regulatory role of lncH19 in RAC1 alternative splicing: implication for RAC1B expression in colorectal cancer

    doi: 10.1186/s13046-024-03139-z

    Figure Lengend Snippet: The sequence of the primers used for gene expression analysis

    Article Snippet: After 24 h, cells were transfected with 1.2 µg/ml of H19-pFLAG-CMV-2 expression vector (cat. n° E7033, Sigma-Aldrich, USA), or empty pFLAG-CMV-2 as Negative Control (Sigma-Aldrich).

    Techniques: Sequencing, Expressing

    The sequence of the biotin-labeled  H19  probes used for RNA pull-down assays

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: Regulatory role of lncH19 in RAC1 alternative splicing: implication for RAC1B expression in colorectal cancer

    doi: 10.1186/s13046-024-03139-z

    Figure Lengend Snippet: The sequence of the biotin-labeled H19 probes used for RNA pull-down assays

    Article Snippet: After 24 h, cells were transfected with 1.2 µg/ml of H19-pFLAG-CMV-2 expression vector (cat. n° E7033, Sigma-Aldrich, USA), or empty pFLAG-CMV-2 as Negative Control (Sigma-Aldrich).

    Techniques: Sequencing

    RBFOX2 is involved in RAC1 alternative splicing in CRC cells. ( A - B - D , E - F - H ) QRT-PCR for the indicated mRNA in CRC cells, silenced for RBFOX2 with two different siRNA. Graphs show 2-ΔΔct calculated in silenced cells respect to relative controls (Normality test and t-test). ( C , F ) Western Blot and densitometric analyses for RAC1B in SW620 and HCT116 silenced for RBFOX2 and relative controls. For densitometric analysis data are represented as normalized OD. ( I - L ) qRT-PCR of the indicated genes in SW620 and HCT116 silenced for H19, the graphs represent the 2^- ΔΔ ct of the indicated calculated respect the expression in control cells. ( M ) Western Blot of RAC1b protein levels in CRC cells (SW620 and HCT116) in H19 silenced cells and relative control cells. Statistical analyses were performed using normality test and t-test, p-value is shown in th e graphs

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: Regulatory role of lncH19 in RAC1 alternative splicing: implication for RAC1B expression in colorectal cancer

    doi: 10.1186/s13046-024-03139-z

    Figure Lengend Snippet: RBFOX2 is involved in RAC1 alternative splicing in CRC cells. ( A - B - D , E - F - H ) QRT-PCR for the indicated mRNA in CRC cells, silenced for RBFOX2 with two different siRNA. Graphs show 2-ΔΔct calculated in silenced cells respect to relative controls (Normality test and t-test). ( C , F ) Western Blot and densitometric analyses for RAC1B in SW620 and HCT116 silenced for RBFOX2 and relative controls. For densitometric analysis data are represented as normalized OD. ( I - L ) qRT-PCR of the indicated genes in SW620 and HCT116 silenced for H19, the graphs represent the 2^- ΔΔ ct of the indicated calculated respect the expression in control cells. ( M ) Western Blot of RAC1b protein levels in CRC cells (SW620 and HCT116) in H19 silenced cells and relative control cells. Statistical analyses were performed using normality test and t-test, p-value is shown in th e graphs

    Article Snippet: After 24 h, cells were transfected with 1.2 µg/ml of H19-pFLAG-CMV-2 expression vector (cat. n° E7033, Sigma-Aldrich, USA), or empty pFLAG-CMV-2 as Negative Control (Sigma-Aldrich).

    Techniques: Alternative Splicing, Quantitative RT-PCR, Western Blot, Expressing, Control

    Overexpression of lncH19 upregulates RAC1B expression. ( A ) qRT-PCR to analyze H19 mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( B ) qRT-PCR to analyze RAC1B mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( C ) Western Blot for RAC1B in CRC cells (SW620 and HCT116), transfected with lncH19 or empty vector. lncH19 overexpression promotes RAC1B nuclear localization. ( D ) Representative confocal microscopy images of anti-RAC1b immunofluorescence showed nuclear localization of RAC1b in lncH19-overexpressing CRC cells, SW620 (upper panel) and HCT116 (lower panel). The analysis of the RAC1B nuclear signal is reported on the histogram. ( E ) Western blot analysis and densitometric analyses for RAC1B in nuclear protein fractions of CRC cells (SW620 and HCT116) overexpressing H19 cells and relative control cells. E-F) Overexpression of lncH19 upregulate CiclinD and c-Myc expression through RAC1B activity qRT-PCR for the indicated genes in SW620 ( F ) and HCT116 ( G ) transfected with pH19 or empty vector and treated or not with RAC1B inhibitor. Statistical analyses were performed using: normality test, one sample t-test to compare different conditions to pEmpty untreated cells, and Two-tails unpaired t-test to compare two groups *; p-value is shown in the graphs

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: Regulatory role of lncH19 in RAC1 alternative splicing: implication for RAC1B expression in colorectal cancer

    doi: 10.1186/s13046-024-03139-z

    Figure Lengend Snippet: Overexpression of lncH19 upregulates RAC1B expression. ( A ) qRT-PCR to analyze H19 mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( B ) qRT-PCR to analyze RAC1B mRNA levels in CRC cells (SW620 and HCT116) transfected with lncH19 or empty vector. ( C ) Western Blot for RAC1B in CRC cells (SW620 and HCT116), transfected with lncH19 or empty vector. lncH19 overexpression promotes RAC1B nuclear localization. ( D ) Representative confocal microscopy images of anti-RAC1b immunofluorescence showed nuclear localization of RAC1b in lncH19-overexpressing CRC cells, SW620 (upper panel) and HCT116 (lower panel). The analysis of the RAC1B nuclear signal is reported on the histogram. ( E ) Western blot analysis and densitometric analyses for RAC1B in nuclear protein fractions of CRC cells (SW620 and HCT116) overexpressing H19 cells and relative control cells. E-F) Overexpression of lncH19 upregulate CiclinD and c-Myc expression through RAC1B activity qRT-PCR for the indicated genes in SW620 ( F ) and HCT116 ( G ) transfected with pH19 or empty vector and treated or not with RAC1B inhibitor. Statistical analyses were performed using: normality test, one sample t-test to compare different conditions to pEmpty untreated cells, and Two-tails unpaired t-test to compare two groups *; p-value is shown in the graphs

    Article Snippet: After 24 h, cells were transfected with 1.2 µg/ml of H19-pFLAG-CMV-2 expression vector (cat. n° E7033, Sigma-Aldrich, USA), or empty pFLAG-CMV-2 as Negative Control (Sigma-Aldrich).

    Techniques: Over Expression, Expressing, Quantitative RT-PCR, Transfection, Plasmid Preparation, Western Blot, Confocal Microscopy, Immunofluorescence, Control, Activity Assay