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plko 1 puro constructs  (Addgene inc)


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    Structured Review

    Addgene inc plko 1 puro constructs
    Plko 1 Puro Constructs, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1591 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plasmid+constructs/pLKO%2E1+puro+(Plasmid+%238453)/pmc13010945-62-9-16
    Average 96 stars, based on 1591 article reviews
    plko 1 puro constructs - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    shRNA:

    Article Title: Prohibitin 2 mediates the mitochondrial protective effect of the whey-derived tetrapeptide Gly-Thr-Trp-Tyr.
    Article Snippet: .. These oligonucleotides were phosphorylated, annealed, and inserted into the pLKO.1-puro lentiviral shRNA vector (8453; Addgene) [9]. .. Escherichia coli BL21 (DE3) cells (Thermo Fisher Scientific) transformed with pCold II-PHB1 or pGEX-4T1-PHB2 were cultured at 37◦C until the OD600 reached 0.4–0.6.

    Article Title: DNA replication stress redistributes the histone methyltransferase G9a and activates lineage-specific gene expression
    Article Snippet: .. HRI knockdown was performed using shRNA constructs (TRCN0000010229 and TRCN0000010231 from the Broad Genome Perturbation Platform) expressed from a pLKO.1 backbone (Addgene #8453). ..

    Article Title: CircACVR2A(2-4) regulates stem cell pluripotency by uncoupling CDK-activating kinase functions.
    Article Snippet: .. Short hairpin RNA and circRNA overexpression constructs All human RNA-targeting shRNAs were cloned into pLKO.1puro (Addgene, #8453), which was sequentially digested with Eco RI-HF and Age I-HF (New England Biolabs, Ipswich, MA, USA) in 1 × CutSmart buffer at 37◦C for 1 h and gel- academ ic.oup.com /nar/article/54/19/gkag964/8913154 by guest on 19 O ctober 2026 ..

    Article Title: Fanconi anemia pathway disruption drives lomustine sensitivity in glioma.
    Article Snippet: 209 Apoptosis Analysis 210 Apoptosis signal under CCNU and PIP-199 treatment in different cell lines was assessed with the BD 211 Annexin V/PI detection Kit (BD, Franklin Lakes, NJ, USA) according to the manufacturer’s protocol as 212 previously described.21 Further information can be found in the Supplementary information. .. 213 Primary glioblastoma cultures 214 Primary cultures were generated and treated as previously described and outlined in the 215 Supplementary Methods.19,21 216 shRNA knockdown human cell lines (lentivirus) 217 We introduced shRNA sequences (Supplementary Table ST4) into pLKO.1 puro (gift from Bob 218 Weinberg; Addgene #8453 Watertown, MA, USA) digested with AgeR1 and EcoR1 (New England 219 Biolabs (NEB), Ipswich, MA, US). .. We transfected HEK293FT cells cultured in OptiMEM (Gibco, Carlsbad, 220 CA, US) with 10 μg of transfer plasmid and equimolar amount of psPAX2 and pMD2.G (gift from Didier 221 AC CE PT ED M AN US RI PT academ ic.oup.com /neuro-oncology/advance-article/doi/10.1093/neuonc/noag254/8907305 by guest on 19 O ctober 2026 12 Trono; Addgene #12260 and #12259, Watertown, MA, USA) using Lipofectamine 3000 (Invitrogen, 222 Waltham, MA, USA)

    Plasmid Preparation:

    Article Title: Prohibitin 2 mediates the mitochondrial protective effect of the whey-derived tetrapeptide Gly-Thr-Trp-Tyr.
    Article Snippet: .. These oligonucleotides were phosphorylated, annealed, and inserted into the pLKO.1-puro lentiviral shRNA vector (8453; Addgene) [9]. .. Escherichia coli BL21 (DE3) cells (Thermo Fisher Scientific) transformed with pCold II-PHB1 or pGEX-4T1-PHB2 were cultured at 37◦C until the OD600 reached 0.4–0.6.

    Article Title: LAMTOR2 Reprograms Energy Metabolism to Sustain Hepatocellular Carcinoma Cell Survival
    Article Snippet: Hepatocellular carcinoma (HCC) is characterized by profound metabolic reprogramming to support rapid proliferation and survival under nutrient stress.. However, the central regulatory hubs that coordinate these diverse metabolic programs remain poorly understood.. Here, we identify LAMTOR2 as a critical coordinator of energy metabolism and survival in HCC cells.

    Article Title: Lactate-associated H3K18 lactylation and SYT8 in the temozolomide response of glioblastoma cells.
    Article Snippet: This is a PDF of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability.. This version will undergo additional copyediting, typesetting and review before it is published in its final form.. As such, this version is no longer the Accepted Manuscript, but it is not yet the definitive Version of Record; we are providing this early version to give early visibility of the article.

    Purification:

    Article Title: LAMTOR2 Reprograms Energy Metabolism to Sustain Hepatocellular Carcinoma Cell Survival
    Article Snippet: Hepatocellular carcinoma (HCC) is characterized by profound metabolic reprogramming to support rapid proliferation and survival under nutrient stress.. However, the central regulatory hubs that coordinate these diverse metabolic programs remain poorly understood.. Here, we identify LAMTOR2 as a critical coordinator of energy metabolism and survival in HCC cells.

    Gel Extraction:

    Article Title: LAMTOR2 Reprograms Energy Metabolism to Sustain Hepatocellular Carcinoma Cell Survival
    Article Snippet: Hepatocellular carcinoma (HCC) is characterized by profound metabolic reprogramming to support rapid proliferation and survival under nutrient stress.. However, the central regulatory hubs that coordinate these diverse metabolic programs remain poorly understood.. Here, we identify LAMTOR2 as a critical coordinator of energy metabolism and survival in HCC cells.

    Over Expression:

    Article Title: tRNA dosage regulates lineage dependency and resistance in prostate cancer.
    Article Snippet: .. For overexpression of tRNAArg(UCU) isodecoders, three tandem repeats of tRNA1 Arg(UCU), tRNA2 Arg(UCU), tRNA3 Arg(UCU), tRNA4 Arg(UCU) and tRNA5 Arg(UCU) and their flanking sequences around the genomic loci (±200 bp) (see Supplementary Table 9 for details) were cloned into pLKO.1 puro (Addgene, 8453) following deletion of the U6 promoter region using ClaI and AgeI. ..

    Article Title: CircACVR2A(2-4) regulates stem cell pluripotency by uncoupling CDK-activating kinase functions.
    Article Snippet: .. Short hairpin RNA and circRNA overexpression constructs All human RNA-targeting shRNAs were cloned into pLKO.1puro (Addgene, #8453), which was sequentially digested with Eco RI-HF and Age I-HF (New England Biolabs, Ipswich, MA, USA) in 1 × CutSmart buffer at 37◦C for 1 h and gel- academ ic.oup.com /nar/article/54/19/gkag964/8913154 by guest on 19 O ctober 2026 ..

    Clone Assay:

    Article Title: tRNA dosage regulates lineage dependency and resistance in prostate cancer.
    Article Snippet: .. For overexpression of tRNAArg(UCU) isodecoders, three tandem repeats of tRNA1 Arg(UCU), tRNA2 Arg(UCU), tRNA3 Arg(UCU), tRNA4 Arg(UCU) and tRNA5 Arg(UCU) and their flanking sequences around the genomic loci (±200 bp) (see Supplementary Table 9 for details) were cloned into pLKO.1 puro (Addgene, 8453) following deletion of the U6 promoter region using ClaI and AgeI. ..

    Article Title: Lactate-associated H3K18 lactylation and SYT8 in the temozolomide response of glioblastoma cells.
    Article Snippet: This is a PDF of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability.. This version will undergo additional copyediting, typesetting and review before it is published in its final form.. As such, this version is no longer the Accepted Manuscript, but it is not yet the definitive Version of Record; we are providing this early version to give early visibility of the article.

    Article Title: CircACVR2A(2-4) regulates stem cell pluripotency by uncoupling CDK-activating kinase functions.
    Article Snippet: .. Short hairpin RNA and circRNA overexpression constructs All human RNA-targeting shRNAs were cloned into pLKO.1puro (Addgene, #8453), which was sequentially digested with Eco RI-HF and Age I-HF (New England Biolabs, Ipswich, MA, USA) in 1 × CutSmart buffer at 37◦C for 1 h and gel- academ ic.oup.com /nar/article/54/19/gkag964/8913154 by guest on 19 O ctober 2026 ..

    Knockdown:

    Article Title: DNA replication stress redistributes the histone methyltransferase G9a and activates lineage-specific gene expression
    Article Snippet: .. HRI knockdown was performed using shRNA constructs (TRCN0000010229 and TRCN0000010231 from the Broad Genome Perturbation Platform) expressed from a pLKO.1 backbone (Addgene #8453). ..

    Article Title: Fanconi anemia pathway disruption drives lomustine sensitivity in glioma.
    Article Snippet: 209 Apoptosis Analysis 210 Apoptosis signal under CCNU and PIP-199 treatment in different cell lines was assessed with the BD 211 Annexin V/PI detection Kit (BD, Franklin Lakes, NJ, USA) according to the manufacturer’s protocol as 212 previously described.21 Further information can be found in the Supplementary information. .. 213 Primary glioblastoma cultures 214 Primary cultures were generated and treated as previously described and outlined in the 215 Supplementary Methods.19,21 216 shRNA knockdown human cell lines (lentivirus) 217 We introduced shRNA sequences (Supplementary Table ST4) into pLKO.1 puro (gift from Bob 218 Weinberg; Addgene #8453 Watertown, MA, USA) digested with AgeR1 and EcoR1 (New England 219 Biolabs (NEB), Ipswich, MA, US). .. We transfected HEK293FT cells cultured in OptiMEM (Gibco, Carlsbad, 220 CA, US) with 10 μg of transfer plasmid and equimolar amount of psPAX2 and pMD2.G (gift from Didier 221 AC CE PT ED M AN US RI PT academ ic.oup.com /neuro-oncology/advance-article/doi/10.1093/neuonc/noag254/8907305 by guest on 19 O ctober 2026 12 Trono; Addgene #12260 and #12259, Watertown, MA, USA) using Lipofectamine 3000 (Invitrogen, 222 Waltham, MA, USA)

    Construct:

    Article Title: DNA replication stress redistributes the histone methyltransferase G9a and activates lineage-specific gene expression
    Article Snippet: .. HRI knockdown was performed using shRNA constructs (TRCN0000010229 and TRCN0000010231 from the Broad Genome Perturbation Platform) expressed from a pLKO.1 backbone (Addgene #8453). ..

    Article Title: A natural compound derivative targeting HADHA disrupts mitochondrial homeostasis and suppresses renal cell carcinoma.
    Article Snippet: Ara Jo, Sanjeevram Dhandapani, Ziqin Wang, Hyeryeon Jung, Hongjun Jang, Morgan A. Bailey, Andrew Tran, Brandon Tsai, Jinjae Park, Hyejin Lee, Hye-Jin Park, Yoojin Lim, Dolce Feenaghty, Victor M. Moncada, Damu Wu, Keaton Chien, Nancy Chen, Yunsol Jo, Jiazheng Miao, Zhujun Yao, Jihoon Lee, Karthigayan Shanmugasundaram, Gang Greg Wang, Andrew Armstrong, Daniel George, David Howell, Jiaoti Huang, Michael C. Fitzgerald, Jiyong Hong, Jung Wook Park

    Article Title: CircACVR2A(2-4) regulates stem cell pluripotency by uncoupling CDK-activating kinase functions.
    Article Snippet: .. Short hairpin RNA and circRNA overexpression constructs All human RNA-targeting shRNAs were cloned into pLKO.1puro (Addgene, #8453), which was sequentially digested with Eco RI-HF and Age I-HF (New England Biolabs, Ipswich, MA, USA) in 1 × CutSmart buffer at 37◦C for 1 h and gel- academ ic.oup.com /nar/article/54/19/gkag964/8913154 by guest on 19 O ctober 2026 ..

    Generated:

    Article Title: Fanconi anemia pathway disruption drives lomustine sensitivity in glioma.
    Article Snippet: 209 Apoptosis Analysis 210 Apoptosis signal under CCNU and PIP-199 treatment in different cell lines was assessed with the BD 211 Annexin V/PI detection Kit (BD, Franklin Lakes, NJ, USA) according to the manufacturer’s protocol as 212 previously described.21 Further information can be found in the Supplementary information. .. 213 Primary glioblastoma cultures 214 Primary cultures were generated and treated as previously described and outlined in the 215 Supplementary Methods.19,21 216 shRNA knockdown human cell lines (lentivirus) 217 We introduced shRNA sequences (Supplementary Table ST4) into pLKO.1 puro (gift from Bob 218 Weinberg; Addgene #8453 Watertown, MA, USA) digested with AgeR1 and EcoR1 (New England 219 Biolabs (NEB), Ipswich, MA, US). .. We transfected HEK293FT cells cultured in OptiMEM (Gibco, Carlsbad, 220 CA, US) with 10 μg of transfer plasmid and equimolar amount of psPAX2 and pMD2.G (gift from Didier 221 AC CE PT ED M AN US RI PT academ ic.oup.com /neuro-oncology/advance-article/doi/10.1093/neuonc/noag254/8907305 by guest on 19 O ctober 2026 12 Trono; Addgene #12260 and #12259, Watertown, MA, USA) using Lipofectamine 3000 (Invitrogen, 222 Waltham, MA, USA)



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    Addgene inc yfp tagged dbn drebrin yfp construct
    (A) HEp-2 cells were “mock” infected (NI) or infected with RSV for 24 h, at MOI 1 and processed for IP using M antibodies. Input (1 %), unbound (1 %) and bound (30 %) fractions were loaded on SDS-PAGE and a Western blot was performed using antibodies indicated on the left. Representative of three independent experiments. (B) <t>HEp-2-Drebrin-YFP</t> and HEp-2-YFP cells were infected with RSV for 24 h, at MOI 1 and processed for IP using anti-GFP nanobodies. Input (0,5 %), unbound (0,5 %) and bound (30 %) fractions were loaded on SDS-PAGE and a Western blot was performed using antibodies indicated on the left. Drebrin-YFP and YFP corresponding bands were indicated by an arrow on the left. Representative of three independent experiments.
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    Image Search Results


    (A) HEp-2 cells were “mock” infected (NI) or infected with RSV for 24 h, at MOI 1 and processed for IP using M antibodies. Input (1 %), unbound (1 %) and bound (30 %) fractions were loaded on SDS-PAGE and a Western blot was performed using antibodies indicated on the left. Representative of three independent experiments. (B) HEp-2-Drebrin-YFP and HEp-2-YFP cells were infected with RSV for 24 h, at MOI 1 and processed for IP using anti-GFP nanobodies. Input (0,5 %), unbound (0,5 %) and bound (30 %) fractions were loaded on SDS-PAGE and a Western blot was performed using antibodies indicated on the left. Drebrin-YFP and YFP corresponding bands were indicated by an arrow on the left. Representative of three independent experiments.

    Journal: bioRxiv

    Article Title: The actin-binding protein drebrin interacts with the respiratory syncytial virus matrix protein and promotes virus particle release

    doi: 10.64898/2026.10.05.756730

    Figure Lengend Snippet: (A) HEp-2 cells were “mock” infected (NI) or infected with RSV for 24 h, at MOI 1 and processed for IP using M antibodies. Input (1 %), unbound (1 %) and bound (30 %) fractions were loaded on SDS-PAGE and a Western blot was performed using antibodies indicated on the left. Representative of three independent experiments. (B) HEp-2-Drebrin-YFP and HEp-2-YFP cells were infected with RSV for 24 h, at MOI 1 and processed for IP using anti-GFP nanobodies. Input (0,5 %), unbound (0,5 %) and bound (30 %) fractions were loaded on SDS-PAGE and a Western blot was performed using antibodies indicated on the left. Drebrin-YFP and YFP corresponding bands were indicated by an arrow on the left. Representative of three independent experiments.

    Article Snippet: YFP-tagged DBN (drebrin-YFP) construct has been provided from addgene (#40359).

    Techniques: Infection, SDS Page, Western Blot

    Drebrin promotes viral particle release . (A) Schematic representation of the release assay. HEp-2 cells were transfected with control or specific siRNAs and seeded onto Transwell inserts for 48h (step 1). Cells were then infected with RSV-mCherry at an MOI of 1 (step 2). After washes to remove non-internalized virus, the infected “donor” cells were then placed in contact with target cells (step 3). The number of infected “donor” and “target” cells were quantified based on mCherry fluorescence using the Incucyte S3 system at 20h (step4) and 38h (step 5) post-infection respectively. RSV release efficiency was calculated as the ratio of infected target cells to infected donor cells and normalized to the control siRNA condition. (B) HEp-2 cells were transfected with si NT or drebrin-specific siRNAs (si drebrin) and release assay was performed as described in A. Date are mean ± SD of 6 independent experiments, each point represents mean of triplicates. Y axis represents viral release efficiency (ratio of infected target cells to infected donor cells) normalized to the control siRNA condition. (C) release assay was performed with HEp-2-YFP and HEp-2-Drebrin-YFP cells. Data are mean ± SD of 4 independent experiments done in triplicates. Y axis represents viral release efficiency (ratio of infected target cells to infected donor cells) normalized to the control siRNA condition. (B-C) A one-sample t-test was performed. * : P < 0.05; ** : P < 0.001.

    Journal: bioRxiv

    Article Title: The actin-binding protein drebrin interacts with the respiratory syncytial virus matrix protein and promotes virus particle release

    doi: 10.64898/2026.10.05.756730

    Figure Lengend Snippet: Drebrin promotes viral particle release . (A) Schematic representation of the release assay. HEp-2 cells were transfected with control or specific siRNAs and seeded onto Transwell inserts for 48h (step 1). Cells were then infected with RSV-mCherry at an MOI of 1 (step 2). After washes to remove non-internalized virus, the infected “donor” cells were then placed in contact with target cells (step 3). The number of infected “donor” and “target” cells were quantified based on mCherry fluorescence using the Incucyte S3 system at 20h (step4) and 38h (step 5) post-infection respectively. RSV release efficiency was calculated as the ratio of infected target cells to infected donor cells and normalized to the control siRNA condition. (B) HEp-2 cells were transfected with si NT or drebrin-specific siRNAs (si drebrin) and release assay was performed as described in A. Date are mean ± SD of 6 independent experiments, each point represents mean of triplicates. Y axis represents viral release efficiency (ratio of infected target cells to infected donor cells) normalized to the control siRNA condition. (C) release assay was performed with HEp-2-YFP and HEp-2-Drebrin-YFP cells. Data are mean ± SD of 4 independent experiments done in triplicates. Y axis represents viral release efficiency (ratio of infected target cells to infected donor cells) normalized to the control siRNA condition. (B-C) A one-sample t-test was performed. * : P < 0.05; ** : P < 0.001.

    Article Snippet: YFP-tagged DBN (drebrin-YFP) construct has been provided from addgene (#40359).

    Techniques: Release Assay, Transfection, Control, Infection, Virus, Fluorescence

    (A) diagrams of drebrin mutants are shown. ADFH, actin-depolymerizing factor homology domain. ABD1, actin binding domain 1. ABD2, actin binding domain 2. IDD intrinsically disordered domain. Constructs are YFP-tagged at the C-terminus. Numbering is for human drebrin E. (B) HEp-2 cells lines were established with the indicated plasmids and cells were infected with RSV for 24h at MOI 1 and processed for IP using anti-GFP nanobodies. Input (0,5 %), unbound (0,5 %) and bound (30 %) fractions were loaded on SDS-PAGE and Western blotting using antibodies indicated on the left. Representative of three independent experiments. (C) release assay was performed as in with cells expressing indicated plasmids. Data are mean ± SD of 6 independent experiments done in triplicates. Y axis represents viral release efficiency (ratio of infected target cells to infected donor cells) normalized to the control siRNA condition. One-Way ANOVA with Dunnett’s multiple comparisons test and Geisser-Greenhouse correction was performed, ns : P > 0.05, ** : P < 0.01, **** : P < 0.0001.

    Journal: bioRxiv

    Article Title: The actin-binding protein drebrin interacts with the respiratory syncytial virus matrix protein and promotes virus particle release

    doi: 10.64898/2026.10.05.756730

    Figure Lengend Snippet: (A) diagrams of drebrin mutants are shown. ADFH, actin-depolymerizing factor homology domain. ABD1, actin binding domain 1. ABD2, actin binding domain 2. IDD intrinsically disordered domain. Constructs are YFP-tagged at the C-terminus. Numbering is for human drebrin E. (B) HEp-2 cells lines were established with the indicated plasmids and cells were infected with RSV for 24h at MOI 1 and processed for IP using anti-GFP nanobodies. Input (0,5 %), unbound (0,5 %) and bound (30 %) fractions were loaded on SDS-PAGE and Western blotting using antibodies indicated on the left. Representative of three independent experiments. (C) release assay was performed as in with cells expressing indicated plasmids. Data are mean ± SD of 6 independent experiments done in triplicates. Y axis represents viral release efficiency (ratio of infected target cells to infected donor cells) normalized to the control siRNA condition. One-Way ANOVA with Dunnett’s multiple comparisons test and Geisser-Greenhouse correction was performed, ns : P > 0.05, ** : P < 0.01, **** : P < 0.0001.

    Article Snippet: YFP-tagged DBN (drebrin-YFP) construct has been provided from addgene (#40359).

    Techniques: Binding Assay, Construct, Infection, SDS Page, Western Blot, Release Assay, Expressing, Control

    (A) Drebrin-YFP HEp-2 cells were uninfected or infected with RSV at MOI 1 for 24 h. Proteins associated with drebrin-YFP were affinity-purified using GFP nanobody-coupled agarose beads, identified by mass spectrometry, and quantified based on spectral counts obtained for each sample. A log2 fold change was calculated by comparing RSV-infected and uninfected conditions. Only proteins with at least two spectral counts in at least two biological replicates in either condition were included in the analysis. Statistical significance was assessed using a beta-binomial test adapted for spectral count data. Results are presented as a volcano plot. The horizontal dashed gray line indicates the statistical significance threshold ( P < 0.05), whereas the vertical dashed gray lines indicate a twofold difference between infected and uninfected samples. Cellular proteins used in C are indicated in blue. Viral RSV proteins are indicated in black. Results from three independent biological replicates (B) Left: Heat map of RT-qPCR analysis comparing mRNA levels of 17 candidate proteins in RSV-infected and uninfected cells. Blue indicates > 3-fold upregulation and yellow < 3-fold. Right: Heat map of viral replication analysis comparing RSV-mCherry signal in RSV-infected cells treated with interactors-specific siRNA and si NT. Blue indicates replication >140%, brown replication < 60% and yellow 60% < replication >140%. Complete data are shown in Fig S8. (C) HEp-2 cells were depleted with the indicated siRNAs and viral release assay was performed and compared with control conditions. One-Way ANOVA with Dunnett’s multiple comparisons test and Geisser-Greenhouse correction was performed relative to si NT. *** : P <0.001, ns : P >0,05.

    Journal: bioRxiv

    Article Title: The actin-binding protein drebrin interacts with the respiratory syncytial virus matrix protein and promotes virus particle release

    doi: 10.64898/2026.10.05.756730

    Figure Lengend Snippet: (A) Drebrin-YFP HEp-2 cells were uninfected or infected with RSV at MOI 1 for 24 h. Proteins associated with drebrin-YFP were affinity-purified using GFP nanobody-coupled agarose beads, identified by mass spectrometry, and quantified based on spectral counts obtained for each sample. A log2 fold change was calculated by comparing RSV-infected and uninfected conditions. Only proteins with at least two spectral counts in at least two biological replicates in either condition were included in the analysis. Statistical significance was assessed using a beta-binomial test adapted for spectral count data. Results are presented as a volcano plot. The horizontal dashed gray line indicates the statistical significance threshold ( P < 0.05), whereas the vertical dashed gray lines indicate a twofold difference between infected and uninfected samples. Cellular proteins used in C are indicated in blue. Viral RSV proteins are indicated in black. Results from three independent biological replicates (B) Left: Heat map of RT-qPCR analysis comparing mRNA levels of 17 candidate proteins in RSV-infected and uninfected cells. Blue indicates > 3-fold upregulation and yellow < 3-fold. Right: Heat map of viral replication analysis comparing RSV-mCherry signal in RSV-infected cells treated with interactors-specific siRNA and si NT. Blue indicates replication >140%, brown replication < 60% and yellow 60% < replication >140%. Complete data are shown in Fig S8. (C) HEp-2 cells were depleted with the indicated siRNAs and viral release assay was performed and compared with control conditions. One-Way ANOVA with Dunnett’s multiple comparisons test and Geisser-Greenhouse correction was performed relative to si NT. *** : P <0.001, ns : P >0,05.

    Article Snippet: YFP-tagged DBN (drebrin-YFP) construct has been provided from addgene (#40359).

    Techniques: Infection, Affinity Purification, Mass Spectrometry, Analysis, Quantitative RT-PCR, Release Assay, Control, Significance Assay