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bacmid transfection agent promega fugene® hd  (Promega)

 
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    Structured Review

    Promega bacmid transfection agent promega fugene® hd
    Bacmid Transfection Agent Promega Fugene® Hd, supplied by Promega, 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/fugene+hd+transfection+agent/bacmid+transfection+agent+promega+fugene++hd/us12281321-2265-13-13
    Average 90 stars, based on 1 article reviews
    bacmid transfection agent promega fugene® hd - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome
    Article Snippet: .. 0.5 μg and 1.0 μg plasmid DNA per 100 μl total transfection volume was used with 2 to 3μl FuGene HD transfection agent per well (Promega, Madison, USA, product-nr. E2311). .. 48 h after transfection, cells were paraformaldehyde xed and immuno uorescence staining of Flag-tag was performed by standard protocols for cell HEK 293T Page 11/23 cell cultures (primary antibody: monoclonal DYKDDDDK Tag Recombinant, Thermo Fisher Scienti c, Waltham, USA, product-nr. 701629, RRID: AB_2532497, 1:250 dilution (2.5 μg/ml); secondary antibody: goat anti-rabbit-Alexa 594, Invitrogen/Thermo Fischer Scienti c, product-nr. A-11012, RRID: AB_2534079, 1:1000 dilution (1 μg/ml)) and DAPI (Sigma-Aldrich, St. Louis, USA; product-nr. D9542, 1:5000 dilution (4 μg/ml)).

    Article Title: How insulin-like growth factor I binds to a hybrid insulin receptor type 1 insulin-like growth factor receptor
    Article Snippet: M.C.L.’s laboratory has a funded agreement with Eli Lilly and Company to conduct research not connected to this publication. .. Cells were transfected with complexes of plasmid DNA using FuGENE HD transfection agent (Promega, Australia) and cells were exposed to 25 mM methionine sulphoximine in Lonza DMEM (High Glucose) media containing 13 GS supplement (Merck) and 10%dialysed FBS (Life Technologies). .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Mouse monoclonal antibody 24-60 (anti-human IGF-1R) (Soos et al., 1992) N/A Mouse monoclonal antibody 83-7 (anti-human IR) (Soos et al., 1986) N/A Mouse monoclonal antibody 18-44 (anti-human IR) (Soos et al., 1986) N/A Mouse monoclonal antibody 9E10 (anti-c-myc) CSIRO Laboratories, Parkville, Australia ATCC CRL1729 IRDye 800CW Goat anti-mouse IgG LI-COR Biosciences Cat# 926-32210; RRID: AB_621842 Chemicals, peptides, and recombinant proteins 9E10 c-myc epitope peptide, sequence EQKLISEEDL (>75% purity) Genscript N/A 18-44 IR epitope peptide, sequence TSPEEHRPFE (>70% purity) Genscript N/A Receptor grade IGF-I GroPep Cat# CM001 IGF-I (King et al., 1992) N/A Eu-IGF-I (Denley et al., 2004) N/A Insulin Novo Nordisk Actrapid Fetal calf serum Scientifix FBSFR-62147A G418 ThermoFisher Scientific 10131035 Puromycin ThermoFisher Scientific A1113802 L-Methionine sulfoximine Merck GSS-1015-F Eu-N1-ITC chelate Perkin Elmer 1244-302 DELFIA Enhancement Solution Perkin Elmer 1244-104 Fetal Bovine Serum, dialyzed ThermoFisher Scientific 30067344 DMEM with Glucose, without L-Glutamine Lonza 12-614F GS Supplement Merck GSS-1016-C Trypsin Gold Promega Cat# V5280 FuGENE HD transfection agent Promega E2311 ProSep-vA resin Millipore Deposited data Crystal structure of apo IGF-1R ectodomain (Xu et al., 2018) PDB: 5U8R Crystal structure of apo IR ectodomain (Croll et al., 2016) PDB: 4ZXB CryoEM structure of IGF-II bound IGF-1R (head region; open conformation (Xu et al., 2020) PDB: 6VXG Model: IGF-I-bound HybZip, head region This study PDB: 7S0Q Model: IGF-I-bound HybZip, leg region This study PDB: 7S8V Map: IGF-I-bound HybZip, head region This study EMD-24791 Map: IGF-I-bound HybZip, leg region This study EMD-24927 Experimental models: Cell lines BALB/c3T3 cells overexpressing IGF-IR (Pietrzkowski et al., 1992) P6 IGF-IR null mouse fibroblasts overexpressing the human IR-B In-house; (Denley et al., 2004) R-IR-B CHO-Lec8 ATCC ATCC CRL-1737 Recombinant DNA (Continued on next page) Structure 30, 1098–1108.e1–e6, August 4, 2022 e1

    Article Title: Screening of Membrane Protein Production by Comparison of Transient Expression in Insect and Mammalian Cells
    Article Snippet: .. In the reaction mixture, each pOPINE-GOI-3C-eGFP-His6 baculovirus transfer plasmid (500/750 ng) was added to Bsu 36I (New England Biolabs, Frankfurt-am-Main, Germany, #R0524S), linearized empty DsRed bacmid (500 ng) (the bacmid was a kind gift from Prof. Ian Jones) diluted in 100 μL Sf-900 II SFM (Gibco TM Sf-900 TM II, Thermo Fisher Scientific, Bremen, Germany) following the addition of 5 μL FuGENE HD Transfection Agent (Promega, Walldorf, Germany, #E2312). ..

    Article Title: A multiplex single-cell RNA-Seq pharmacotranscriptomics pipeline for drug discovery.
    Article Snippet: For the silencing of CAV1 (L-003467-00-0005, Dharmacon Reagents), EGFR (L-003114-00-0005, Dharmacon Reagents) or the control (D-00181010-05, Dharmacon Reagents), an ON-TARGETplus siRNA smart pool of four siRNAs per target was used at the final concentration of 12.5 nM using DharmaFECT 1 transfection reagent (T-2001-02, Dharmacon Reagents). .. For plasmid transfections, CAV1 was cloned with a Flag tag into the pCDNA3.1 expression plasmid and 2 μg of purified DNA per well in six-well plates or 100 ng of purified DNA per well in 96-well plates was transfected using FuGENE HD transfection agent (E2311, Promega) as per the manufacturer’s instructions. .. Equal amounts of pSG5 plasmid (216201, Agilent Technologies) were used in transfections as a control.

    Article Title: Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome.
    Article Snippet: .. 0.5 μg and 1.0 μg plasmid DNA per 100 μl total transfection volume was used with 2 to 3 μl FuGene HD transfection agent per well (Promega, Madison, USA, product-nr. E2311). .. 48 h after transfection, cells were paraformaldehyde fixed and immunofluorescence staining of Flag-tag was performed by standard protocols for cell HEK 293T cell cultures (primary antibody: monoclonal DYKDDDDK Tag Recombinant, Thermo Fisher Scientific, Waltham, USA, product-nr. 701629, RRID: AB_2532497, 1:250 dilution (2.5 μg/ml); secondary antibody: goat anti-rabbit-Alexa 594, Invitrogen/Thermo Fischer Scientific, product-nr. A-11012, RRID: AB_2534079, 1:1000 dilution (1 μg/ml)) and DAPI (Sigma-Aldrich, St. Louis, USA; product-nr. D9542, 1:5000 dilution (4 μg/ ml)).

    Transfection:

    Article Title: Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome
    Article Snippet: .. 0.5 μg and 1.0 μg plasmid DNA per 100 μl total transfection volume was used with 2 to 3μl FuGene HD transfection agent per well (Promega, Madison, USA, product-nr. E2311). .. 48 h after transfection, cells were paraformaldehyde xed and immuno uorescence staining of Flag-tag was performed by standard protocols for cell HEK 293T Page 11/23 cell cultures (primary antibody: monoclonal DYKDDDDK Tag Recombinant, Thermo Fisher Scienti c, Waltham, USA, product-nr. 701629, RRID: AB_2532497, 1:250 dilution (2.5 μg/ml); secondary antibody: goat anti-rabbit-Alexa 594, Invitrogen/Thermo Fischer Scienti c, product-nr. A-11012, RRID: AB_2534079, 1:1000 dilution (1 μg/ml)) and DAPI (Sigma-Aldrich, St. Louis, USA; product-nr. D9542, 1:5000 dilution (4 μg/ml)).

    Article Title: Targeting ZDHHC9 enhances anti-PD-L1 immunotherapy efficacy by reprogramming the tumour microenvironment
    Article Snippet: .. Transfection was performed using the Polybrene and FuGENE HD transfection agent (Promega, USA), according to the manufacturer’s protocol. ..

    Article Title: How insulin-like growth factor I binds to a hybrid insulin receptor type 1 insulin-like growth factor receptor
    Article Snippet: M.C.L.’s laboratory has a funded agreement with Eli Lilly and Company to conduct research not connected to this publication. .. Cells were transfected with complexes of plasmid DNA using FuGENE HD transfection agent (Promega, Australia) and cells were exposed to 25 mM methionine sulphoximine in Lonza DMEM (High Glucose) media containing 13 GS supplement (Merck) and 10%dialysed FBS (Life Technologies). .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Mouse monoclonal antibody 24-60 (anti-human IGF-1R) (Soos et al., 1992) N/A Mouse monoclonal antibody 83-7 (anti-human IR) (Soos et al., 1986) N/A Mouse monoclonal antibody 18-44 (anti-human IR) (Soos et al., 1986) N/A Mouse monoclonal antibody 9E10 (anti-c-myc) CSIRO Laboratories, Parkville, Australia ATCC CRL1729 IRDye 800CW Goat anti-mouse IgG LI-COR Biosciences Cat# 926-32210; RRID: AB_621842 Chemicals, peptides, and recombinant proteins 9E10 c-myc epitope peptide, sequence EQKLISEEDL (>75% purity) Genscript N/A 18-44 IR epitope peptide, sequence TSPEEHRPFE (>70% purity) Genscript N/A Receptor grade IGF-I GroPep Cat# CM001 IGF-I (King et al., 1992) N/A Eu-IGF-I (Denley et al., 2004) N/A Insulin Novo Nordisk Actrapid Fetal calf serum Scientifix FBSFR-62147A G418 ThermoFisher Scientific 10131035 Puromycin ThermoFisher Scientific A1113802 L-Methionine sulfoximine Merck GSS-1015-F Eu-N1-ITC chelate Perkin Elmer 1244-302 DELFIA Enhancement Solution Perkin Elmer 1244-104 Fetal Bovine Serum, dialyzed ThermoFisher Scientific 30067344 DMEM with Glucose, without L-Glutamine Lonza 12-614F GS Supplement Merck GSS-1016-C Trypsin Gold Promega Cat# V5280 FuGENE HD transfection agent Promega E2311 ProSep-vA resin Millipore Deposited data Crystal structure of apo IGF-1R ectodomain (Xu et al., 2018) PDB: 5U8R Crystal structure of apo IR ectodomain (Croll et al., 2016) PDB: 4ZXB CryoEM structure of IGF-II bound IGF-1R (head region; open conformation (Xu et al., 2020) PDB: 6VXG Model: IGF-I-bound HybZip, head region This study PDB: 7S0Q Model: IGF-I-bound HybZip, leg region This study PDB: 7S8V Map: IGF-I-bound HybZip, head region This study EMD-24791 Map: IGF-I-bound HybZip, leg region This study EMD-24927 Experimental models: Cell lines BALB/c3T3 cells overexpressing IGF-IR (Pietrzkowski et al., 1992) P6 IGF-IR null mouse fibroblasts overexpressing the human IR-B In-house; (Denley et al., 2004) R-IR-B CHO-Lec8 ATCC ATCC CRL-1737 Recombinant DNA (Continued on next page) Structure 30, 1098–1108.e1–e6, August 4, 2022 e1

    Article Title: Screening of Membrane Protein Production by Comparison of Transient Expression in Insect and Mammalian Cells
    Article Snippet: .. In the reaction mixture, each pOPINE-GOI-3C-eGFP-His6 baculovirus transfer plasmid (500/750 ng) was added to Bsu 36I (New England Biolabs, Frankfurt-am-Main, Germany, #R0524S), linearized empty DsRed bacmid (500 ng) (the bacmid was a kind gift from Prof. Ian Jones) diluted in 100 μL Sf-900 II SFM (Gibco TM Sf-900 TM II, Thermo Fisher Scientific, Bremen, Germany) following the addition of 5 μL FuGENE HD Transfection Agent (Promega, Walldorf, Germany, #E2312). ..

    Article Title: A multiplex single-cell RNA-Seq pharmacotranscriptomics pipeline for drug discovery.
    Article Snippet: For the silencing of CAV1 (L-003467-00-0005, Dharmacon Reagents), EGFR (L-003114-00-0005, Dharmacon Reagents) or the control (D-00181010-05, Dharmacon Reagents), an ON-TARGETplus siRNA smart pool of four siRNAs per target was used at the final concentration of 12.5 nM using DharmaFECT 1 transfection reagent (T-2001-02, Dharmacon Reagents). .. For plasmid transfections, CAV1 was cloned with a Flag tag into the pCDNA3.1 expression plasmid and 2 μg of purified DNA per well in six-well plates or 100 ng of purified DNA per well in 96-well plates was transfected using FuGENE HD transfection agent (E2311, Promega) as per the manufacturer’s instructions. .. Equal amounts of pSG5 plasmid (216201, Agilent Technologies) were used in transfections as a control.

    Article Title: Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome.
    Article Snippet: .. 0.5 μg and 1.0 μg plasmid DNA per 100 μl total transfection volume was used with 2 to 3 μl FuGene HD transfection agent per well (Promega, Madison, USA, product-nr. E2311). .. 48 h after transfection, cells were paraformaldehyde fixed and immunofluorescence staining of Flag-tag was performed by standard protocols for cell HEK 293T cell cultures (primary antibody: monoclonal DYKDDDDK Tag Recombinant, Thermo Fisher Scientific, Waltham, USA, product-nr. 701629, RRID: AB_2532497, 1:250 dilution (2.5 μg/ml); secondary antibody: goat anti-rabbit-Alexa 594, Invitrogen/Thermo Fischer Scientific, product-nr. A-11012, RRID: AB_2534079, 1:1000 dilution (1 μg/ml)) and DAPI (Sigma-Aldrich, St. Louis, USA; product-nr. D9542, 1:5000 dilution (4 μg/ ml)).

    Article Title: How insulin-like growth factor I binds to a hybrid insulin receptor type 1 insulin-like growth factor receptor
    Article Snippet: Trypsin Gold , Promega , Cat# V5280. .. FuGENE HD transfection agent , Promega , E2311. .. ProSep-vA resin , Millipore , .

    Article Title: Identification of Inhibitors of the Schistosoma mansoni VKR2 Kinase Domain
    Article Snippet: .. For virus construction, 100 ng of the pOPINF_VKR2 baculovirus transfer plasmids (1 μg/μL) were mixed with 250 ng Bsu36I linearized DsRed bacmid (0.1 μg/μL) and 1.5 uL FuGENE HD Transfection Agent (Promega) in 50 μL Sf-900 II SFM. ..

    Clone Assay:

    Article Title: A multiplex single-cell RNA-Seq pharmacotranscriptomics pipeline for drug discovery.
    Article Snippet: For the silencing of CAV1 (L-003467-00-0005, Dharmacon Reagents), EGFR (L-003114-00-0005, Dharmacon Reagents) or the control (D-00181010-05, Dharmacon Reagents), an ON-TARGETplus siRNA smart pool of four siRNAs per target was used at the final concentration of 12.5 nM using DharmaFECT 1 transfection reagent (T-2001-02, Dharmacon Reagents). .. For plasmid transfections, CAV1 was cloned with a Flag tag into the pCDNA3.1 expression plasmid and 2 μg of purified DNA per well in six-well plates or 100 ng of purified DNA per well in 96-well plates was transfected using FuGENE HD transfection agent (E2311, Promega) as per the manufacturer’s instructions. .. Equal amounts of pSG5 plasmid (216201, Agilent Technologies) were used in transfections as a control.

    FLAG-tag:

    Article Title: A multiplex single-cell RNA-Seq pharmacotranscriptomics pipeline for drug discovery.
    Article Snippet: For the silencing of CAV1 (L-003467-00-0005, Dharmacon Reagents), EGFR (L-003114-00-0005, Dharmacon Reagents) or the control (D-00181010-05, Dharmacon Reagents), an ON-TARGETplus siRNA smart pool of four siRNAs per target was used at the final concentration of 12.5 nM using DharmaFECT 1 transfection reagent (T-2001-02, Dharmacon Reagents). .. For plasmid transfections, CAV1 was cloned with a Flag tag into the pCDNA3.1 expression plasmid and 2 μg of purified DNA per well in six-well plates or 100 ng of purified DNA per well in 96-well plates was transfected using FuGENE HD transfection agent (E2311, Promega) as per the manufacturer’s instructions. .. Equal amounts of pSG5 plasmid (216201, Agilent Technologies) were used in transfections as a control.

    Expressing:

    Article Title: A multiplex single-cell RNA-Seq pharmacotranscriptomics pipeline for drug discovery.
    Article Snippet: For the silencing of CAV1 (L-003467-00-0005, Dharmacon Reagents), EGFR (L-003114-00-0005, Dharmacon Reagents) or the control (D-00181010-05, Dharmacon Reagents), an ON-TARGETplus siRNA smart pool of four siRNAs per target was used at the final concentration of 12.5 nM using DharmaFECT 1 transfection reagent (T-2001-02, Dharmacon Reagents). .. For plasmid transfections, CAV1 was cloned with a Flag tag into the pCDNA3.1 expression plasmid and 2 μg of purified DNA per well in six-well plates or 100 ng of purified DNA per well in 96-well plates was transfected using FuGENE HD transfection agent (E2311, Promega) as per the manufacturer’s instructions. .. Equal amounts of pSG5 plasmid (216201, Agilent Technologies) were used in transfections as a control.

    Purification:

    Article Title: A multiplex single-cell RNA-Seq pharmacotranscriptomics pipeline for drug discovery.
    Article Snippet: For the silencing of CAV1 (L-003467-00-0005, Dharmacon Reagents), EGFR (L-003114-00-0005, Dharmacon Reagents) or the control (D-00181010-05, Dharmacon Reagents), an ON-TARGETplus siRNA smart pool of four siRNAs per target was used at the final concentration of 12.5 nM using DharmaFECT 1 transfection reagent (T-2001-02, Dharmacon Reagents). .. For plasmid transfections, CAV1 was cloned with a Flag tag into the pCDNA3.1 expression plasmid and 2 μg of purified DNA per well in six-well plates or 100 ng of purified DNA per well in 96-well plates was transfected using FuGENE HD transfection agent (E2311, Promega) as per the manufacturer’s instructions. .. Equal amounts of pSG5 plasmid (216201, Agilent Technologies) were used in transfections as a control.

    Virus:

    Article Title: Identification of Inhibitors of the Schistosoma mansoni VKR2 Kinase Domain
    Article Snippet: .. For virus construction, 100 ng of the pOPINF_VKR2 baculovirus transfer plasmids (1 μg/μL) were mixed with 250 ng Bsu36I linearized DsRed bacmid (0.1 μg/μL) and 1.5 uL FuGENE HD Transfection Agent (Promega) in 50 μL Sf-900 II SFM. ..



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    In vitro <t>transfection</t> of HEK 293T cells with CMV:MSGN1 (WT)-FLAG-tag and CMV:MSGN1 p.(Arg125Leu)-FLAG-tag plasmids at different concentrations. A Immunofluorescence showing expression of tagged MSGN1 proteins (WT) or p.(Arg125Leu) after 48h of transfection. Corresponding experimental controls are shown in Additional file : Fig. S3A. B Quantification of MSGN1 localization in transfected cells. Fluorescence signals in a by single z-plane were visualized by confocal laser-scanning microscopy and subsequently signal intensity was measured in single cells (cyto: cytoplasm; nuc: nucleus) and outside of cells (bg: background). Graphs show signal intensity measurements of the RFP channel (MSGN1 Flag-Tag) of 30 cells per experimental group and 30 background positions. Signal intensity measurements of the corresponding DAPI channel for nucleus identification are given in Additional file : Fig S3B. Values are given in Additional file : Excel file S1
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    In vitro <t>transfection</t> of HEK 293T cells with CMV:MSGN1 (WT)-FLAG-tag and CMV:MSGN1 p.(Arg125Leu)-FLAG-tag plasmids at different concentrations. A Immunofluorescence showing expression of tagged MSGN1 proteins (WT) or p.(Arg125Leu) after 48h of transfection. Corresponding experimental controls are shown in Additional file : Fig. S3A. B Quantification of MSGN1 localization in transfected cells. Fluorescence signals in a by single z-plane were visualized by confocal laser-scanning microscopy and subsequently signal intensity was measured in single cells (cyto: cytoplasm; nuc: nucleus) and outside of cells (bg: background). Graphs show signal intensity measurements of the RFP channel (MSGN1 Flag-Tag) of 30 cells per experimental group and 30 background positions. Signal intensity measurements of the corresponding DAPI channel for nucleus identification are given in Additional file : Fig S3B. Values are given in Additional file : Excel file S1
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    Image Search Results


    In vitro transfection of HEK 293T cells with CMV:MSGN1 (WT)-FLAG-tag and CMV:MSGN1 p.(Arg125Leu)-FLAG-tag plasmids at different concentrations. A Immunofluorescence showing expression of tagged MSGN1 proteins (WT) or p.(Arg125Leu) after 48h of transfection. Corresponding experimental controls are shown in Additional file : Fig. S3A. B Quantification of MSGN1 localization in transfected cells. Fluorescence signals in a by single z-plane were visualized by confocal laser-scanning microscopy and subsequently signal intensity was measured in single cells (cyto: cytoplasm; nuc: nucleus) and outside of cells (bg: background). Graphs show signal intensity measurements of the RFP channel (MSGN1 Flag-Tag) of 30 cells per experimental group and 30 background positions. Signal intensity measurements of the corresponding DAPI channel for nucleus identification are given in Additional file : Fig S3B. Values are given in Additional file : Excel file S1

    Journal: Human Genomics

    Article Title: Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome

    doi: 10.1186/s40246-024-00593-w

    Figure Lengend Snippet: In vitro transfection of HEK 293T cells with CMV:MSGN1 (WT)-FLAG-tag and CMV:MSGN1 p.(Arg125Leu)-FLAG-tag plasmids at different concentrations. A Immunofluorescence showing expression of tagged MSGN1 proteins (WT) or p.(Arg125Leu) after 48h of transfection. Corresponding experimental controls are shown in Additional file : Fig. S3A. B Quantification of MSGN1 localization in transfected cells. Fluorescence signals in a by single z-plane were visualized by confocal laser-scanning microscopy and subsequently signal intensity was measured in single cells (cyto: cytoplasm; nuc: nucleus) and outside of cells (bg: background). Graphs show signal intensity measurements of the RFP channel (MSGN1 Flag-Tag) of 30 cells per experimental group and 30 background positions. Signal intensity measurements of the corresponding DAPI channel for nucleus identification are given in Additional file : Fig S3B. Values are given in Additional file : Excel file S1

    Article Snippet: 0.5 µg and 1.0 µg plasmid DNA per 100 µl total transfection volume was used with 2 to 3 µl FuGene HD transfection agent per well (Promega, Madison, USA, product-nr. E2311).

    Techniques: In Vitro, Transfection, FLAG-tag, Immunofluorescence, Expressing, Fluorescence, Confocal Laser Scanning Microscopy