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3 protocols using pcdna neat1

1

Overexpression and Silencing of NEAT1 and FLT1

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Vectors for the overexpression of NEAT1 (pcDNA-NEAT1) and FLT1 (pcDNA-FLT1), the miR-373 mimic/inhibitor and their respective negative controls (pcDNA, NC mimic and NC inhibitor) were purchased from RiboBio. Small interfering RNAs (siRNAs) targeting NEAT1 and FLT1 (si-NEAT1, si-FLT1) and control si-NC were obtained from GenePharma (Shanghai, China). Trophoblast cells were transfected with these vectors using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA).
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2

NEAT1, miR-370-3p Regulation Protocol

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si-RNA against NEAT1 (si-NEAT1), miR-370-3p mimic (miR-370-3p) and miR-370-3p inhibitor (anti-miR-370-3p), as well as the corresponding controls (si-control, miR-NC, anti-miR-NC), were obtained from GenePharma (Shanghai, China). NEAT1 overexpression plasmid (pcDNA-NEAT1), Irak2 overexpression plasmid (named as pcDNA-Irak2) and matched control (pcDNA-control) were acquired from RiboBio (Guangzhou, China). Cell transfection was performed using Lipofectamine 3000 reagent (Invitrogen, Carlsbad, CA, USA) following the standard manufacturer's protocol.
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3

Modulating NEAT1 and miR-22-3p in Septic AKI

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Small interference RNA (siRNA) for NEAT1 (si-NEAT1) and the control siRNA (si-NC),
miR-22-3p mimic (miR-22-3p) and the control mimic (NC), miR-22-3p inhibitor
(anti-miR-22-3p) and the control inhibitor (anti-NC), NEAT1 overexpression vector
(pcDNA-NEAT1), and the empty vector (pcDNA-NC) were purchased from RiboBio
(Guangzhou, China). All plasmids and oligonucleotides were transfected into an
LPS-induced septic AKI model using Lipofectamine 2000 reagent (Invitrogen, Carlsbad,
CA, USA).
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