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EMU077021

MISSION® esiRNA

targeting mouse Atad2

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About This Item

NACRES:
NA.51
UNSPSC Code:
41105324
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description

Powered by Eupheria Biotech

Quality Level

100

product line

MISSION®

form

lyophilized powder

esiRNA cDNA target sequence

CAAGCAAAATAGACTTGAAAGCAACATAGACTTGAAAAATAACTCAAGTTCCTCTAATATTGAGAATGAACTTGAAGAGCCTAAGGAAACTACGGAGGGCACAGAACTGAGAAAAGACAGGATTGTTTGCAGGGGTGATGCCTCTGCCTCCCAGGTCACAGACATTCCCGAAGACAGTGAATCAAAAGAAATGGATTTTCTGCGGATGACTCTAGCTAGAGGTTCCCAGGTAGAGCAGCAGGAGCTCATCAGTATGGAGCAGGCTCTGGCCATCCTCTCTCAGCCGACACCCTCACTTGTGCTGGACCACAAGCAGTTAACAAATATTTTGAAGACGGTTGTTAAAAAAAGTCAGAAATATAATATATTCCAACTGGAGAATTTGTATGCAGTAATCAGCCAGTGTATTTATGAGCACCGCAGGGACTATGACAAAACAGCGCTTGTTC

Ensembl | mouse accession no.

ENSMUSG00000022360

NCBI accession no.

NM_027435

shipped in

ambient

storage temp.

−20°C

Gene Information

mouse ... ATAD2(70472), Atad2(70472)

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

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Le Zheng et al.
Oncology reports, 33(5), 2337-2344 (2015-03-31)
The ATPase family AAA domain-containing protein 2 (ATAD2) is associated with many cellular processes, such as cell proliferation, invasion and migration. However, the molecular biological function of the ATAD2 gene in cervical cancer is unclear. The purpose of this study
Wen-Jing Lu et al.
Oncotarget, 6(39), 41722-41735 (2015-10-27)
The ATPase family, AAA domain containing 2 (ATAD2) is highly expressed in multiple cancers. We aim to understand the clinical and biological significance of ATAD2 over-expression in hepatocellular carcinoma (HCC), as a means to validate it as a therapeutic target