shoe gait analysis system Search Results


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OmicsLink™ shRNA clone collections include lentiviral and non-viral vector-based shRNA constructs against genome-wide human, mouse and rat genes. shRNA of varying lengths (19 to 29 bases) were designed using a proprietary algorithm to make shRNA
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<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Mirna Mimic Negative Control Mimic Nc, supplied by Ribobio co, 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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<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Brooks Defyance 3, supplied by Brooks Sports Inc, 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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Average 90 stars, based on 1 article reviews
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<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Online Genetic Testing 23andme, supplied by 23andMe, 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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Average 90 stars, based on 1 article reviews
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Tekscan Inc shoe gait analysis system
<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Shoe Gait Analysis System, supplied by Tekscan Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/shoe+gait+analysis+system/in+shoe+system/10__24002_slash_ijis__v8i1__11505-218-5-1
Average 86 stars, based on 1 article reviews
shoe gait analysis system - by Bioz Stars, 2026-09
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CIR Systems gait rite, version 4.5
<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Gait Rite, Version 4.5, supplied by CIR Systems, 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/shoe+gait+analysis+system/gait+rite++version+4+5/ppr0946104-59-8-14
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gait rite, version 4.5 - by Bioz Stars, 2026-09
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Tektronix inc 20 ghz bandwidth single-shot oscilloscope tektronix dpo72004
<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
20 Ghz Bandwidth Single Shot Oscilloscope Tektronix Dpo72004, supplied by Tektronix inc, 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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Siemens AG electone
<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Electone, supplied by Siemens AG, 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/shoe+gait+analysis+system/electone/10__1055_slash_s___2001___14982-88-9-43
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<t>MiR-206</t> and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of <t>miRNA</t> inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).
Jeni Mcp Detectors, supplied by PHOTONIS Inc, 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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Average 90 stars, based on 1 article reviews
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OmicsLink™ shRNA clone collections include lentiviral and non-viral vector-based shRNA constructs against genome-wide human, mouse and rat genes. shRNA of varying lengths (19 to 29 bases) were designed using a proprietary algorithm to make shRNA
  Buy from Supplier

Image Search Results


MiR-206 and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of miRNA inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).

Journal: Frontiers in Pharmacology

Article Title: Inhibition of 6-phosphogluconate Dehydrogenase Reverses Cisplatin Resistance in Ovarian and Lung Cancer

doi: 10.3389/fphar.2017.00421

Figure Lengend Snippet: MiR-206 and miR-613 directly inhibit the expression of 6PGD through its 3′UTR. (A,B) qRT-PCR analysis of miR-206 and miR-613 expression in OV2008 and C13 ∗ cells (A) and A549 and A549DDP cells (B) . (C,D) The effects of miRNAs on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with 100 nM Mimic Negative control (Mimic NC) and 100 nM miR-206 and miR-613 in C13 ∗ (C) and A549DDP (D) cells, respectively. (E,F) The effects of miRNA inhibitors on 6PGD mRNA, protein expression and enzyme activity, were determined at 48 h after transfected with Inhibitor negative control (Inhibitor NC) and miR-206 inhibitor and miR-613 inhibitor in OV2008 cells (E) and A549 cells (F) , respectively. (G) 293T cells were co-transfected with Renilla luciferase plasmid and a firefly luciferase reporter plasmid containing either wild-type or mutant 6PGD 3′UTR (indicated as pGL3-6PGD-3′UTR-wt and pGL3-6PGD-3′UTR-mu) with either control or miR-206 or miR-613. Luciferase activity was conducted at 24 h after transfection. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).

Article Snippet: The miR-206, miR-613 and miRNA Mimic Negative Control (Mimic NC, miRNA Mimic Negative Controls show the minimal homology to all known miRNAs of miRBase 18.0, and it is a crucial experimental control for miRNA “gain-of-function” studies)and miR-206 inhibitor, miR-613 inhibitor and miRNA Inhibitor Negative Control (Inhibitor NC, micrOFF TM miRNA Inhibitor Negative Control is designed for minimum homology to the miRNAs being studied, and thus an indispensable control for miRNA functional studies) were purchased from RiboBio Co. Ltd. Lipofectamine RNAiMAX transfection reagent was purchased from Thermo Fisher Scientific (catalog number: 13778-150).

Techniques: Expressing, Quantitative RT-PCR, Activity Assay, Transfection, Negative Control, Luciferase, Plasmid Preparation, Mutagenesis, Control

miR-206 and miR-613 have rewired cellular metabolism by targeting 6PGD. (A,B) C13 ∗ (A) and A549DDP (B) cell lines were transfected with Mimic NC, miR-206 and miR-613, respectively. The effects of miRNAs on NADPH/NADP + ratio, lactate production and intracellular ATP levels were determined. (C,D) OV2008 (C) and A549 (D) cell lines were transfected with Inhibitor NC and miR-206 inhibitor and miR-613 inhibitor, respectively. The effects of miRNA inhibitors on NADPH/NADP + ratio, lactate production and intracellular ATP levels were determined. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).

Journal: Frontiers in Pharmacology

Article Title: Inhibition of 6-phosphogluconate Dehydrogenase Reverses Cisplatin Resistance in Ovarian and Lung Cancer

doi: 10.3389/fphar.2017.00421

Figure Lengend Snippet: miR-206 and miR-613 have rewired cellular metabolism by targeting 6PGD. (A,B) C13 ∗ (A) and A549DDP (B) cell lines were transfected with Mimic NC, miR-206 and miR-613, respectively. The effects of miRNAs on NADPH/NADP + ratio, lactate production and intracellular ATP levels were determined. (C,D) OV2008 (C) and A549 (D) cell lines were transfected with Inhibitor NC and miR-206 inhibitor and miR-613 inhibitor, respectively. The effects of miRNA inhibitors on NADPH/NADP + ratio, lactate production and intracellular ATP levels were determined. Error bars represent mean values ± SD from three replicates of each sample ( ∗ P < 0.05; ∗∗ P < 0.01; ∗∗∗ P < 0.001).

Article Snippet: The miR-206, miR-613 and miRNA Mimic Negative Control (Mimic NC, miRNA Mimic Negative Controls show the minimal homology to all known miRNAs of miRBase 18.0, and it is a crucial experimental control for miRNA “gain-of-function” studies)and miR-206 inhibitor, miR-613 inhibitor and miRNA Inhibitor Negative Control (Inhibitor NC, micrOFF TM miRNA Inhibitor Negative Control is designed for minimum homology to the miRNAs being studied, and thus an indispensable control for miRNA functional studies) were purchased from RiboBio Co. Ltd. Lipofectamine RNAiMAX transfection reagent was purchased from Thermo Fisher Scientific (catalog number: 13778-150).

Techniques: Transfection