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Key Documents

Safety Information

EMU158121

Sigma-Aldrich

MISSION® esiRNA

targeting mouse Dtx3l

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About This Item

UNSPSC Code:
41105324
NACRES:
NA.51

description

Powered by Eupheria Biotech

Quality Level

product line

MISSION®

form

lyophilized powder

esiRNA cDNA target sequence

CTAACTCTGTTGACTCAGTTGTCCAAAAGATCTTTCTTGCTGTGACCGCTGAGCTGAACTGTGACCTGCTCTCTAAAGAGCAGAGAGCATCTATAACCACTGTCTGCCCTCACATCATCAAAAGCATGGAGGGTAGTGATGGAATTAAGAAGGTGTGTGGCAACTTCAAAGATATTGAAAAGATACATCACTTCTTGAGTGAGCAGCTTTTGGAACGGGAGCAGAAACGGAAGGGAAGCGAGCAGAAACGGAAGTGCGCCCCACAGAAACACACACCTCCCGATGTGGAGCGGGAGCCCCCTGATCAGAGCAGTATTCAAGTTCCTGTGCTTCTCCTTGAATATTTCAAGCATGTTAATCCGGGTAGACTAGAGTTCATAGAGTACAAATTTGGTGTAAACATTGAAATCCAAGCTAGTTCTCCCAATATGGTCACTGTAGGCTTCACCTCCAGCCCATTTGGCAACGTAGAAGAAGCAAGTCAGTCCTTTGTCAGAGACTTTCAGAAAT

Ensembl | mouse 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 Code

10 - Combustible liquids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

EMU158121-20UG:
EMU158121-50UG:


Certificates of Analysis (COA)

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Danielle P Johnson et al.
Oncotarget, 6(7), 4863-4887 (2015-01-22)
Gain-of-function mutations in the catalytic site of EZH2 (Enhancer of Zeste Homologue 2), is observed in about 22% of diffuse large B-cell lymphoma (DLBCL) cases. Here we show that selective inhibition of histone deacetylase 1,2 (HDAC1,2) activity using a small

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