human vcl Search Results


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Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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Cusabio e cadherin
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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OriGene vinculin (vcl) (nm_003373) human untagged clone
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
Vinculin (Vcl) (Nm 003373) Human Untagged Clone, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Genecopoeia mirna 3´utr target expression clone for human vcl
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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OriGene vinculin (vcl) (nm_003373) human tagged orf clone
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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ZenBio primary rabbit anti human vcl antibodies
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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OriGene vinculin (vcl) (nm_003373) human recombinant protein
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
Vinculin (Vcl) (Nm 003373) Human Recombinant Protein, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ZenBio primary rabbit anti-human vcl antibodies 380393
Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of <t>VCL,</t> Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase <t>reporter</t> <t>plasmids</t> containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).
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Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of VCL, Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase reporter plasmids containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).

Journal: Biochimica et biophysica acta. Gene regulatory mechanisms

Article Title: Impaired cell migration and structural defects in myeloid cells overexpressing miR-30b and miR-142-3p.

doi: 10.1016/j.bbagrm.2020.194628

Figure Lengend Snippet: Fig. 5. miR-142-3p directly regulate genes involved in cell migration, phagocytosis and cell polarity. (A–C; Upper panel) Sequence alignment of predicted miR-142- 3p binding sites in the 3′UTR of VCL, Dab2 and Skap2. Only the binding sites with mfe < −20 kcal/mol are shown. (A–C; Lower panel) HEK293 cells were co- transfected with dual luciferase reporter plasmids containing 3′UTR of VCL, Dab2 and Skap2 or control vector and miR-142-3p or control mimic. After 36 h, cell lysates were prepared to measure renilla and firefly luciferase activity. Renilla activity was normalized to firefly activity and the ratios were subsequently normalized to empty vector transfected with miR-142-3p mimic set as 1. Data are expressed as ± SEM of four independent transfections. Student's t-test was conducted to calculate p-values. *p < 0.05, **p < 0.01, ***p < 0.001. (D) Expression of VCL, Dab2 and Skap2 in MΦ by western blot. Day 7 differentiated cells were transfected with miR-142-3p mimic or control mimic. Cell lysates were prepared after 36 h of transfection and VCL, Dab2 and Skap2 levels were detected by immunoblotting. The expression level of GAPDH was included as loading control. (E) The corresponding densitometric analysis by Image Lab software is also shown. Data are means ± SEM of three independent experiments (*p < 0.05, **p < 0.01; compared with the control mimic).

Article Snippet: All transfections were performed in quadruplicate using 0.5 μL Lipofectamine 2000 (Invitrogen), 120 ng dual luciferase reporter control (CmiT000001-MT06 miRNA Target clone control vector for pEZX-MT06) or plasmids containing human VCL (NM_003373.3; HmiT018467-MT06), human DAB2 (NM_001244871.1; HmiT055467-MT06) or human SKAP2 (NM_001303468.1; HmiT067400-MT06; All from GeneCopoeia Incorporated, Rockville, MD, USA) were co-transfected with a final concentration of 1 pmol, 5 pmol and 10 pmol of synthetic miR-142-3p or control mimics (10 pmol) (Qiagen).

Techniques: Migration, Sequencing, Binding Assay, Transfection, Luciferase, Control, Plasmid Preparation, Activity Assay, Expressing, Western Blot, Software