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mko2 coding sequence (Addgene inc)

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Addgene inc mko2 coding sequence

MIA PaCa-2 expression levels of ELAVL1 and GLS from RNA-Seq data ( a , mean and S.E.M.) and heatmap ( b ) with bidirectional clustering of singscores from KEGG Metabolic Pathways and scaled ELAVL1 expression. The letter ‘Q’ marks pathways that involve glutamine from (Control n = 4; Knockout n = 3). The dendrograms represent full bidirectional complete clustering based on correlation values. c Chromosome 2 indicating GLS loci and exon structure for KGA and GAC isoforms. Bellow, exon differential expression after ELAVL1 knockdown in MIA PaCa-2 or HeLa cells. Asterisks denote FDR < 0.05. d , above, Western blot of doxycycline-inducible ELAVL1 -silenced breast cancer cell lines (MDA-MB-231 and BT549) using two shRNAs, displaying a marked decrease in KGA protein level, accompanied by an increase in GAC. d , below, Western blot of constitutively silenced ELAVL1 breast cancer cell lines, grouped by telaglenastat resistance, which was defined elsewhere . Arrows indicate KGA and GAC isoforms and HuR-specific bands and western blots repeated at least two times with reproducible results. e Scheme for CRISPR-mediated knock-in of the <t>mKO2-P2A-BleoR</t> cassette into GLS exon 19 to produce the KGA-mKO2 fusion protein. f Increase and decrease in cellular fluorescence after ELAVL1 ectopic expression (bottom) or sh ELAVL1 -mediated transient silencing (top), respectively, in HEK293T knock-in cells, number independent cells evaluated per condition >1433. Representative images on the right. The scale bar is 50 μm. g Cell cycle analysis of BT549 knock-in cells KGA levels (evaluated by mKO2 fluorescence) are enhanced in S-G2/M phases, as expected , . Representative images in bottom part, with HiLo lookup table for DNA staining, one cell with higher DNA content and higher KGA content and the opposite example below, confirming the functionality of the system. Box plots represent the interquartile range; the vertical curve is the kernel density of the distribution, and the dark horizontal line denotes the median. Each dot represents an individual cell. Statistical significance derived from bootstrapped DEXSeq ( c ) or Two-sided Welch’s t -test ( f ). * p < 0.05, ** p < 0.01, *** p < 0.0001.

Mko2 Coding Sequence, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 4 article reviews

mko2 coding sequence - by Bioz Stars, 2026-03

93/100 stars

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1) Product Images from "HuR controls glutaminase RNA metabolism"

Article Title: HuR controls glutaminase RNA metabolism

Journal: Nature Communications

doi: 10.1038/s41467-024-49874-x

Figure Legend Snippet: MIA PaCa-2 expression levels of ELAVL1 and GLS from RNA-Seq data ( a , mean and S.E.M.) and heatmap ( b ) with bidirectional clustering of singscores from KEGG Metabolic Pathways and scaled ELAVL1 expression. The letter ‘Q’ marks pathways that involve glutamine from (Control n = 4; Knockout n = 3). The dendrograms represent full bidirectional complete clustering based on correlation values. c Chromosome 2 indicating GLS loci and exon structure for KGA and GAC isoforms. Bellow, exon differential expression after ELAVL1 knockdown in MIA PaCa-2 or HeLa cells. Asterisks denote FDR < 0.05. d , above, Western blot of doxycycline-inducible ELAVL1 -silenced breast cancer cell lines (MDA-MB-231 and BT549) using two shRNAs, displaying a marked decrease in KGA protein level, accompanied by an increase in GAC. d , below, Western blot of constitutively silenced ELAVL1 breast cancer cell lines, grouped by telaglenastat resistance, which was defined elsewhere . Arrows indicate KGA and GAC isoforms and HuR-specific bands and western blots repeated at least two times with reproducible results. e Scheme for CRISPR-mediated knock-in of the mKO2-P2A-BleoR cassette into GLS exon 19 to produce the KGA-mKO2 fusion protein. f Increase and decrease in cellular fluorescence after ELAVL1 ectopic expression (bottom) or sh ELAVL1 -mediated transient silencing (top), respectively, in HEK293T knock-in cells, number independent cells evaluated per condition >1433. Representative images on the right. The scale bar is 50 μm. g Cell cycle analysis of BT549 knock-in cells KGA levels (evaluated by mKO2 fluorescence) are enhanced in S-G2/M phases, as expected , . Representative images in bottom part, with HiLo lookup table for DNA staining, one cell with higher DNA content and higher KGA content and the opposite example below, confirming the functionality of the system. Box plots represent the interquartile range; the vertical curve is the kernel density of the distribution, and the dark horizontal line denotes the median. Each dot represents an individual cell. Statistical significance derived from bootstrapped DEXSeq ( c ) or Two-sided Welch’s t -test ( f ). * p < 0.05, ** p < 0.01, *** p < 0.0001.

Techniques Used: Expressing, RNA Sequencing, Control, Knock-Out, Quantitative Proteomics, Knockdown, Western Blot, CRISPR, Knock-In, Fluorescence, Cell Cycle Assay, Staining, Derivative Assay

a Relative quantification of BT549 mRNA levels following doxycycline-inducible silencing of ELAVL1 , using qPCR for two distinct shRNA sequences. b HuR was immunoprecipitated (western blot above, arrows indicate HuR and IgG heavy chain). The control IgG were used from rabbit, in opposing to the mouse anti-HuR antibody. Quantification of mRNA derived from 3′UTR KGA regions immunoprecipitated bound in HuR from ( c ) PC-3 cells using agarose gel and ( d ) from BT549 using qRT-PCR. Quantification of mRNA derived from 3′UTR GAC regions immunoprecipitated bound in HuR from ( e ) PC-3 cells using agarose gel and ( f ) from BT549 using qRT-PCR. Agarose gel from PC-3 ( g ) and q-RT-PCR from BT549 ( h ) revealed that HuR binds to its mRNA (as already published elsewhere ) in addition to GLS intron 14. i In vitro FRAP analysis of recombinant mKO2-HuR incubated with in vitro transcribed control RNA or intron 14. The bar plot (right) denotes T 1/2 recovery times. Statistical significance derived from Two-sided Welch’s t-test ( a , d , f , h , and i ), error bars are SEM; qRT-PCR assays were evaluated in triplicate; otherwise, each point represents a replicate. * p < 0.05, ** p < 0.01, *** p < 0.0001.

Figure Legend Snippet: a Relative quantification of BT549 mRNA levels following doxycycline-inducible silencing of ELAVL1 , using qPCR for two distinct shRNA sequences. b HuR was immunoprecipitated (western blot above, arrows indicate HuR and IgG heavy chain). The control IgG were used from rabbit, in opposing to the mouse anti-HuR antibody. Quantification of mRNA derived from 3′UTR KGA regions immunoprecipitated bound in HuR from ( c ) PC-3 cells using agarose gel and ( d ) from BT549 using qRT-PCR. Quantification of mRNA derived from 3′UTR GAC regions immunoprecipitated bound in HuR from ( e ) PC-3 cells using agarose gel and ( f ) from BT549 using qRT-PCR. Agarose gel from PC-3 ( g ) and q-RT-PCR from BT549 ( h ) revealed that HuR binds to its mRNA (as already published elsewhere ) in addition to GLS intron 14. i In vitro FRAP analysis of recombinant mKO2-HuR incubated with in vitro transcribed control RNA or intron 14. The bar plot (right) denotes T 1/2 recovery times. Statistical significance derived from Two-sided Welch’s t-test ( a , d , f , h , and i ), error bars are SEM; qRT-PCR assays were evaluated in triplicate; otherwise, each point represents a replicate. * p < 0.05, ** p < 0.01, *** p < 0.0001.

Techniques Used: Quantitative Proteomics, shRNA, Immunoprecipitation, Western Blot, Control, Derivative Assay, Agarose Gel Electrophoresis, Quantitative RT-PCR, Reverse Transcription Polymerase Chain Reaction, In Vitro, Recombinant, Incubation

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Journal: Nature Communications

Article Title: HuR controls glutaminase RNA metabolism

doi: 10.1038/s41467-024-49874-x

Figure Lengend Snippet: MIA PaCa-2 expression levels of ELAVL1 and GLS from RNA-Seq data ( a , mean and S.E.M.) and heatmap ( b ) with bidirectional clustering of singscores from KEGG Metabolic Pathways and scaled ELAVL1 expression. The letter ‘Q’ marks pathways that involve glutamine from (Control n = 4; Knockout n = 3). The dendrograms represent full bidirectional complete clustering based on correlation values. c Chromosome 2 indicating GLS loci and exon structure for KGA and GAC isoforms. Bellow, exon differential expression after ELAVL1 knockdown in MIA PaCa-2 or HeLa cells. Asterisks denote FDR < 0.05. d , above, Western blot of doxycycline-inducible ELAVL1 -silenced breast cancer cell lines (MDA-MB-231 and BT549) using two shRNAs, displaying a marked decrease in KGA protein level, accompanied by an increase in GAC. d , below, Western blot of constitutively silenced ELAVL1 breast cancer cell lines, grouped by telaglenastat resistance, which was defined elsewhere . Arrows indicate KGA and GAC isoforms and HuR-specific bands and western blots repeated at least two times with reproducible results. e Scheme for CRISPR-mediated knock-in of the mKO2-P2A-BleoR cassette into GLS exon 19 to produce the KGA-mKO2 fusion protein. f Increase and decrease in cellular fluorescence after ELAVL1 ectopic expression (bottom) or sh ELAVL1 -mediated transient silencing (top), respectively, in HEK293T knock-in cells, number independent cells evaluated per condition >1433. Representative images on the right. The scale bar is 50 μm. g Cell cycle analysis of BT549 knock-in cells KGA levels (evaluated by mKO2 fluorescence) are enhanced in S-G2/M phases, as expected , . Representative images in bottom part, with HiLo lookup table for DNA staining, one cell with higher DNA content and higher KGA content and the opposite example below, confirming the functionality of the system. Box plots represent the interquartile range; the vertical curve is the kernel density of the distribution, and the dark horizontal line denotes the median. Each dot represents an individual cell. Statistical significance derived from bootstrapped DEXSeq ( c ) or Two-sided Welch’s t -test ( f ). * p < 0.05, ** p < 0.01, *** p < 0.0001.

Article Snippet: Primary antibodies used for immunofluorescence and immunoblotting were Vinculin (Abcam ab18058), Actin (Abcam ab3280), GLS (Abcam ab156876), GAC (RheaBiotech IM-0322), KGA (RheaBiotech IM-0519), HuR (Molecular Probes mp21277 and Cell Signaling 12582), and V5 (Life Technologies 46-1157). pLKO.1 puro was a gift from Bob Weinberg (Addgene plasmid # 8453); pLKO.1-blast, used in GAC silencing experiment was a gift from Keith Mostov (Addgene plasmid # 26655); Tet-pLKO-puro was a gift from Dmitri Wiederschain (Addgene plasmid # 21915); psPAX2 was a gift from Didier Trono (Addgene plasmid # 12260); pMD2.G was a gift from Didier Trono (Addgene plasmid # 12259); pUMVC was a gift from Robert A. Weinberg (Addgene plasmid # 8449); pCMV-VSV-G was a gift from Robert Weinbeg (Addgene plasmid # 8454); pQC mKorange IX was a gift from Connie Cepko (Addgene plasmid # 37344), previously modified by replacing the mKO2 coding sequence with an empty MCS , generating pQC MCS IRES Puro (Addgene # 110343) and pQC V5 MCS IRES Puro (Addgene # 110342).

Techniques: Expressing, RNA Sequencing, Control, Knock-Out, Quantitative Proteomics, Knockdown, Western Blot, CRISPR, Knock-In, Fluorescence, Cell Cycle Assay, Staining, Derivative Assay

Journal: Nature Communications

Article Title: HuR controls glutaminase RNA metabolism

doi: 10.1038/s41467-024-49874-x

Figure Lengend Snippet: a Relative quantification of BT549 mRNA levels following doxycycline-inducible silencing of ELAVL1 , using qPCR for two distinct shRNA sequences. b HuR was immunoprecipitated (western blot above, arrows indicate HuR and IgG heavy chain). The control IgG were used from rabbit, in opposing to the mouse anti-HuR antibody. Quantification of mRNA derived from 3′UTR KGA regions immunoprecipitated bound in HuR from ( c ) PC-3 cells using agarose gel and ( d ) from BT549 using qRT-PCR. Quantification of mRNA derived from 3′UTR GAC regions immunoprecipitated bound in HuR from ( e ) PC-3 cells using agarose gel and ( f ) from BT549 using qRT-PCR. Agarose gel from PC-3 ( g ) and q-RT-PCR from BT549 ( h ) revealed that HuR binds to its mRNA (as already published elsewhere ) in addition to GLS intron 14. i In vitro FRAP analysis of recombinant mKO2-HuR incubated with in vitro transcribed control RNA or intron 14. The bar plot (right) denotes T 1/2 recovery times. Statistical significance derived from Two-sided Welch’s t-test ( a , d , f , h , and i ), error bars are SEM; qRT-PCR assays were evaluated in triplicate; otherwise, each point represents a replicate. * p < 0.05, ** p < 0.01, *** p < 0.0001.

Techniques: Quantitative Proteomics, shRNA, Immunoprecipitation, Western Blot, Control, Derivative Assay, Agarose Gel Electrophoresis, Quantitative RT-PCR, Reverse Transcription Polymerase Chain Reaction, In Vitro, Recombinant, Incubation

Synaptome Mapping Pipeline (A) Endogenous PSD95 and SAP102 were genetically tagged with eGFP (green) and mKO2 (magenta), respectively. These postsynaptic proteins assemble into signaling complexes at excitatory synapses. (B–D) Mice were crossed, and synaptic puncta (confocal image) expressing the fluorescent proteins were imaged in brain sections (B), analyzed (C), and stored and distributed (D).

Journal: Neuron

Article Title: Architecture of the Mouse Brain Synaptome

doi: 10.1016/j.neuron.2018.07.007

Figure Lengend Snippet: Synaptome Mapping Pipeline (A) Endogenous PSD95 and SAP102 were genetically tagged with eGFP (green) and mKO2 (magenta), respectively. These postsynaptic proteins assemble into signaling complexes at excitatory synapses. (B–D) Mice were crossed, and synaptic puncta (confocal image) expressing the fluorescent proteins were imaged in brain sections (B), analyzed (C), and stored and distributed (D).

Article Snippet: phmKO2-MN1 vector carrying mKO2 coding sequence , MBL , Cat# AM-V0146-NP.

Techniques: Expressing

Journal: Neuron

Article Title: Architecture of the Mouse Brain Synaptome

doi: 10.1016/j.neuron.2018.07.007

Figure Lengend Snippet:

Article Snippet: phmKO2-MN1 vector carrying mKO2 coding sequence , MBL , Cat# AM-V0146-NP.

Techniques: Western Blot, Recombinant, Plasmid Preparation, Sequencing, Software

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