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EHU018121

Sigma-Aldrich

MISSION® esiRNA

targeting human FOXF2

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About This Item

UNSPSC Code:
41105324
NACRES:
NA.51

description

Powered by Eupheria Biotech

product line

MISSION®

form

lyophilized powder

esiRNA cDNA target sequence

ACTCGCTGGAGCAGAGCTACTTGCACCAGAACGCTCGCGAGGACCTCTCAGTGGGACTGCCCCGTTACCAGCATCACTCTACTCCAGTGTGTGACAGAAAAGATTTCGTCCTCAACTTCAATGGGATTTCTTCTTTCCATCCCTCAGCTAGCGGGTCGTATTATCACCATCACCACCAGAGCGTCTGTCAGGATATTAAGCCCTGCGTCATGTGAACGGAAAGAGGCCAAGCGATGGCCGCTCTCTCCTCTCCCCTCCTCAGAGGGGGCAGATAGAAACTGGGACGGATTCAAGTCACATGCACGCGGATAGCAGTAAGCCACACACCTGCCACTTAGCCAGAATGCCCAGGATCGCGTTGGTCACTGTTATTTGCCTACTGCTGGAAGAAGGACAACCGCTGGCAAGGTAGCGTTCCCCAATCT

Ensembl | human accession no.

NCBI accession no.

shipped in

ambient

storage temp.

−20°C

Gene Information

General description

MISSION® esiRNA are endoribonuclease prepared siRNA. They are a heterogeneous mixture of siRNA that all target the same mRNA sequence. These multiple silencing triggers lead to highly-specific and effective gene silencing.

For additional details as well as to view all available esiRNA options, please visit SigmaAldrich.com/esiRNA.

Legal Information

MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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De-Zhi Zheng et al.
Immunopharmacology and immunotoxicology, 40(5), 408-414 (2018-11-30)
To reveal other miR-130b-mediated signaling pathway in the involvement of wear particle-induced inflammation and osteolysis. Particle-induced osteolysis (PIO) mice model was established. Secretion levels of TNF-α, IL-1β, IL-6, and IL-10 were measured by ELISA. miR-130b and forkhead box F2 (FOXF2)
Akira Higashimori et al.
Cancer research, 78(7), 1643-1656 (2018-01-28)
DNA methylation has been identified as a hallmark of gastric cancer (GC). Identifying genes that are repressed by DNA promoter methylation is essential in providing insights into the molecular pathogenesis of gastric cancer. Using genome-wide methylation studies, we identified that

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