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Sirna oligonucleotides

Manufactured by Integrated DNA Technologies
Sourced in Israel, United States

SiRNA oligonucleotides are short, double-stranded RNA molecules designed to mediate RNA interference (RNAi) by silencing the expression of specific genes. They function by binding to and degrading the target mRNA, thereby preventing the production of the corresponding protein.

Automatically generated - may contain errors

4 protocols using sirna oligonucleotides

1

siRNA Knockdown of RHAMM in SN12L1 Cells

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siRNA oligonucleotides were purchased from Integrated DNA Technologies (Skokie, IL). SN12L1 cells were seeded at a density of 2.4 × 106 cells in six-well plates, grown for 24 h, and transfected with siRNA oligos targeting RHAMM (siRHAMM) using Lipofectamine RNAiMAX (ThermoFisher, Waltham, MA) according to the manufacturer’s instructions. As a negative control, cells were transfected with scrambled RNA oligos. siRHAMM oligos were: 5′-GUCAAGAAUCAUGGAAGUAAACATC3′ and 3′CACAGUUCUUAGUACCUUCAUUUGUAG-5′.
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2

siRNA Knockdown of Cell Cycle Regulators

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The following siRNA oligonucleotides targeting HRP‐3,28, 29E2F1, and Cyclin E were synthesized by Integrated DNA Technologies Inc: siHRP‐3, 5′‐GGCCAUGUGUAAAGUUUAAUU‐3′; siE2F1, 5′‐GUCACGCUAUGAGACCUCACUG‐3′; and siCyclin E, 5′‐AAGUGCUACUGCCGCAGUAUCC‐3′. The siRNA duplexes were transfected into cells using Metafectene reagent (Biontex) according to the manufacturer's guidelines.
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3

Targeted siRNA Oligonucleotide Synthesis

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siRNA oligonucleotides targeting Mdm20, Nat5 and Rictor were chemically synthesized (Integrated DNA Technologies/IDT), and the sequences are shown in S1 Table. Control siRNA was purchased from IDT.
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4

Targeted siRNA Knockdown of GFP, RET, and GFRα4

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TT cells that were engineered to express GFP were electroporated with siRNA oligonucleotides (Integrated DNA Technologies, Coralville, IA, USA) targeting GFP (positive control), RET, GFRα4, or with a non-targeting siRNA (negative control). Twenty-four hours later, cells were lysed, and mRNA was isolated for measurement of RET and GFRα4 by qPCR. Cells were also maintained in culture and counted 7 days later to assess proliferation.
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