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pcib lentiviral expression vector  (Addgene inc)


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    Structured Review

    Addgene inc pcib lentiviral expression vector
    Pcib Lentiviral Expression Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pcib/pLenti+CMVie-IRES-BlastR+alt+MCS+(Plasmid+%23120862)/us12552834-520-20-24
    Average 92 stars, based on 2 article reviews
    pcib lentiviral expression vector - by Bioz Stars, 2026-10
    92/100 stars

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    Related Articles

    Over Expression:

    Article Title: Breast tumor stiffness instructs bone metastasis via maintenance of mechanical conditioning
    Article Snippet: .. To assay human RUNX2 isoform overexpression we subcloned human RUNX2-I (MRIPV isoform, GeneCopoeia #EX-I2457-Lv105) into pCIB (Addgene #119863), and the human-equivalent ERK-target sites were made using Quikchange and subcloning: wild-type pCIB-hsRUNX2, pCIB-hsRUNX2-S280A-S298A (RUNX2-SA) and hsRUNX2-S280E-S298E (RUNX2-SE) which were used for additional in vitro validations (Figures S9B and S9C; note that human RUNX2-SA does not run faster by SDS-PAGE than human RUNX2-WT or human RUNX2-SE, as is observed with mouse isoforms, yet the effects on target gene expression is consistent for both species). .. For live-cell actin dynamics, we used pLenti Lifeact-iRFP670-BlastR (Addgene #84385).

    Subcloning:

    Article Title: Breast tumor stiffness instructs bone metastasis via maintenance of mechanical conditioning
    Article Snippet: .. To assay human RUNX2 isoform overexpression we subcloned human RUNX2-I (MRIPV isoform, GeneCopoeia #EX-I2457-Lv105) into pCIB (Addgene #119863), and the human-equivalent ERK-target sites were made using Quikchange and subcloning: wild-type pCIB-hsRUNX2, pCIB-hsRUNX2-S280A-S298A (RUNX2-SA) and hsRUNX2-S280E-S298E (RUNX2-SE) which were used for additional in vitro validations (Figures S9B and S9C; note that human RUNX2-SA does not run faster by SDS-PAGE than human RUNX2-WT or human RUNX2-SE, as is observed with mouse isoforms, yet the effects on target gene expression is consistent for both species). .. For live-cell actin dynamics, we used pLenti Lifeact-iRFP670-BlastR (Addgene #84385).

    In Vitro:

    Article Title: Breast tumor stiffness instructs bone metastasis via maintenance of mechanical conditioning
    Article Snippet: .. To assay human RUNX2 isoform overexpression we subcloned human RUNX2-I (MRIPV isoform, GeneCopoeia #EX-I2457-Lv105) into pCIB (Addgene #119863), and the human-equivalent ERK-target sites were made using Quikchange and subcloning: wild-type pCIB-hsRUNX2, pCIB-hsRUNX2-S280A-S298A (RUNX2-SA) and hsRUNX2-S280E-S298E (RUNX2-SE) which were used for additional in vitro validations (Figures S9B and S9C; note that human RUNX2-SA does not run faster by SDS-PAGE than human RUNX2-WT or human RUNX2-SE, as is observed with mouse isoforms, yet the effects on target gene expression is consistent for both species). .. For live-cell actin dynamics, we used pLenti Lifeact-iRFP670-BlastR (Addgene #84385).

    SDS Page:

    Article Title: Breast tumor stiffness instructs bone metastasis via maintenance of mechanical conditioning
    Article Snippet: .. To assay human RUNX2 isoform overexpression we subcloned human RUNX2-I (MRIPV isoform, GeneCopoeia #EX-I2457-Lv105) into pCIB (Addgene #119863), and the human-equivalent ERK-target sites were made using Quikchange and subcloning: wild-type pCIB-hsRUNX2, pCIB-hsRUNX2-S280A-S298A (RUNX2-SA) and hsRUNX2-S280E-S298E (RUNX2-SE) which were used for additional in vitro validations (Figures S9B and S9C; note that human RUNX2-SA does not run faster by SDS-PAGE than human RUNX2-WT or human RUNX2-SE, as is observed with mouse isoforms, yet the effects on target gene expression is consistent for both species). .. For live-cell actin dynamics, we used pLenti Lifeact-iRFP670-BlastR (Addgene #84385).

    Targeted Gene Expression:

    Article Title: Breast tumor stiffness instructs bone metastasis via maintenance of mechanical conditioning
    Article Snippet: .. To assay human RUNX2 isoform overexpression we subcloned human RUNX2-I (MRIPV isoform, GeneCopoeia #EX-I2457-Lv105) into pCIB (Addgene #119863), and the human-equivalent ERK-target sites were made using Quikchange and subcloning: wild-type pCIB-hsRUNX2, pCIB-hsRUNX2-S280A-S298A (RUNX2-SA) and hsRUNX2-S280E-S298E (RUNX2-SE) which were used for additional in vitro validations (Figures S9B and S9C; note that human RUNX2-SA does not run faster by SDS-PAGE than human RUNX2-WT or human RUNX2-SE, as is observed with mouse isoforms, yet the effects on target gene expression is consistent for both species). .. For live-cell actin dynamics, we used pLenti Lifeact-iRFP670-BlastR (Addgene #84385).

    Generated:

    Article Title: The CIP2A-TOPBP1 axis safeguards chromosome stability and is a synthetic lethal target for BRCA-mutated cancer.
    Article Snippet: 1Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.. 2Department of Gynecology, University Hospital and University of Zurich, Schlieren, Switzerland.. 3Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

    Cloning:

    Article Title: The CIP2A-TOPBP1 axis safeguards chromosome stability and is a synthetic lethal target for BRCA-mutated cancer.
    Article Snippet: 1Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.. 2Department of Gynecology, University Hospital and University of Zurich, Schlieren, Switzerland.. 3Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

    Mutagenesis:

    Article Title: The CIP2A-TOPBP1 axis safeguards chromosome stability and is a synthetic lethal target for BRCA-mutated cancer.
    Article Snippet: 1Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.. 2Department of Gynecology, University Hospital and University of Zurich, Schlieren, Switzerland.. 3Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

    other:

    Article Title: Breast tumor stiffness instructs bone metastasis via maintenance of mechanical conditioning
    Article Snippet: pCIB , , Addgene Cat: 119863.



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    Image Search Results


    Auxin inhibitors halt prehaustorium development in Phelipanche aegyptiaca . (A) The radicle tips in P. aegyptiaca after 3 days of treatment with gradient concentrations of p ‐chlorophenoxyisobutyric acid (PCIB) and 2,3,5‐triiodobenzoic acid (TIBA) (0.2, 0.1, 0.01 mM) combined with 2,6‐dimethoxy‐1,4‐benzoquinone (DMBQ) (0.01 mM) or indole‐3‐acetic acid (IAA) (0.1 mM). The corresponding control treatments included 0.01 mM DMBQ or 0.1 mM IAA alone. Red arrows indicate swollen radicle tips under various treatments. Scale bar: 500 μm. (B) Expansion rates of radicle tips. (C) Radicle length ( n = 21 seeds). (D) Endogenous IAA content. Data are presented as the mean ± SD (three biological replicates). Groups marked by different letters differ significantly ( p < 0.05) using one‐way ANOVA and Duncan's test. (E) Heatmap showing the hierarchical clustering of auxin‐related gene expression across six treatments: DMBQ + PCIB, DMBQ + TIBA, DMBQ, IAA + PCIB, IAA + TIBA and IAA. The raw data were normalised using Z‐score standardisation. The value ‘0’ represents the overall average expression level of each hormone across all samples. (F) Venn diagram showing the overlap of differentially expressed genes (DEGs) identified from pairwise comparisons: DMBQ + PCIB vs. DMBQ, DMBQ + TIBA vs. DMBQ, IAA + PCIB vs. IAA and IAA + TIBA vs. IAA. (G) KEGG enrichment analysis of 1106 DEGs common to the comparisons.

    Journal: Molecular Plant Pathology

    Article Title: 6‐Hydroxynicotinic Acid From Cucumis melo Inhibits Prehaustorium Formation in Phelipanche aegyptiaca via Disruption of Auxin Signalling Pathway

    doi: 10.1111/mpp.70137

    Figure Lengend Snippet: Auxin inhibitors halt prehaustorium development in Phelipanche aegyptiaca . (A) The radicle tips in P. aegyptiaca after 3 days of treatment with gradient concentrations of p ‐chlorophenoxyisobutyric acid (PCIB) and 2,3,5‐triiodobenzoic acid (TIBA) (0.2, 0.1, 0.01 mM) combined with 2,6‐dimethoxy‐1,4‐benzoquinone (DMBQ) (0.01 mM) or indole‐3‐acetic acid (IAA) (0.1 mM). The corresponding control treatments included 0.01 mM DMBQ or 0.1 mM IAA alone. Red arrows indicate swollen radicle tips under various treatments. Scale bar: 500 μm. (B) Expansion rates of radicle tips. (C) Radicle length ( n = 21 seeds). (D) Endogenous IAA content. Data are presented as the mean ± SD (three biological replicates). Groups marked by different letters differ significantly ( p < 0.05) using one‐way ANOVA and Duncan's test. (E) Heatmap showing the hierarchical clustering of auxin‐related gene expression across six treatments: DMBQ + PCIB, DMBQ + TIBA, DMBQ, IAA + PCIB, IAA + TIBA and IAA. The raw data were normalised using Z‐score standardisation. The value ‘0’ represents the overall average expression level of each hormone across all samples. (F) Venn diagram showing the overlap of differentially expressed genes (DEGs) identified from pairwise comparisons: DMBQ + PCIB vs. DMBQ, DMBQ + TIBA vs. DMBQ, IAA + PCIB vs. IAA and IAA + TIBA vs. IAA. (G) KEGG enrichment analysis of 1106 DEGs common to the comparisons.

    Article Snippet: The experimental groups received 0.1 mM IAA and 0.01 mM DMBQ mixed with 0.2, 0.1, or 0.01 mM PCIB (Shanghai Macklin Biochemical Co. Ltd.) or TIBA (Shanghai Macklin Biochemical Co. Ltd.) for 3 days.

    Techniques: Control, Gene Expression, Expressing

    Effects of IAA and auxin inhibitor on the parasitic ability of Phelipanche aegyptiaca . ( A – C ) Growth status of melon seedlings inoculated with P. aegyptiaca , parasitic damage to their root systems, and developmental status of P. aegyptiaca under treatments with 15 μM PCIB, 0.1 mM IAA, and water (CK), respectively. ( D ) Total number of P. aegyptiaca attachments to the host roots in the three treatments (* p < 0.05). ( E ) Number of P. aegyptiaca attachments to the host roots at different developmental stages in the three treatments (* p < 0.05; ** p < 0.01). S7: P. aegyptiaca emergence; S6: P. aegyptiaca develops a young shoot > 2 cm but has not emerged; S5: Adventitious roots form at the nodules and connect with other roots < 1 cm. ( F ) Plant heights of the host plants under the three treatments (* p < 0.05; ** p < 0.01).

    Journal: Plants

    Article Title: IAA-Mediated Haustorium Formation in Phelipanche aegyptiaca : Transcriptional Insights and Anti-Parasitic Strategies

    doi: 10.3390/plants14111591

    Figure Lengend Snippet: Effects of IAA and auxin inhibitor on the parasitic ability of Phelipanche aegyptiaca . ( A – C ) Growth status of melon seedlings inoculated with P. aegyptiaca , parasitic damage to their root systems, and developmental status of P. aegyptiaca under treatments with 15 μM PCIB, 0.1 mM IAA, and water (CK), respectively. ( D ) Total number of P. aegyptiaca attachments to the host roots in the three treatments (* p < 0.05). ( E ) Number of P. aegyptiaca attachments to the host roots at different developmental stages in the three treatments (* p < 0.05; ** p < 0.01). S7: P. aegyptiaca emergence; S6: P. aegyptiaca develops a young shoot > 2 cm but has not emerged; S5: Adventitious roots form at the nodules and connect with other roots < 1 cm. ( F ) Plant heights of the host plants under the three treatments (* p < 0.05; ** p < 0.01).

    Article Snippet: The experimental design included three treatment groups: the 1 mM IAA aqueous solution treatment group, the 15 μM auxin activity inhibitor p -chlorophenoxyisobutyric acid (PCIB) [ ] (Macklin Biochemical Co., Ltd., Shanghai, China) aqueous solution treatment group, and the control group irrigated with only water.

    Techniques: