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Safety Information

EMU154061

Sigma-Aldrich

MISSION® esiRNA

targeting mouse Tlx2

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About This Item

UNSPSC Code:
41105324
NACRES:
NA.51
Pricing and availability is not currently available.

description

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product line

MISSION®

form

lyophilized powder

esiRNA cDNA target sequence

CTCTTCGCGCTGCAGAATCTGCAGCCCTGGGCGGAAGACAACAAGGTGGCTTCGGTGTCCGGGCTCGCCTCGGTGGTGTGACCGACACCTGCCCGACGAGCGCCAACGTGGCCGGGTGCCGTACCGCCAGCGAAGAGTGAGGAGCAGAAGGCCCGCGGCCCGCGGCCGTCCTCTGAGGCTCTTTGGTCATCAGTGGCCCCTGGCCCACACTCTGACTCCGCCCTTCAAGGTTTTGTTTTGTTTTGTTTAAAAAAAAAAACCCCGCTGAGATGTGGGTTGCAAGAGCAACCTGCAGGATTGTGGATGAAGCAGGGACCCTGCAAGGCTGCGACTTTGCCCTGAGTGGGCTCAGAGCTCAGGTCCTGCTGGGAAGGGACCACAGAGCTGGTGTAAAGGCAGATATCAAAGGACAGCGGGGGAGGGGTAATGGAAGAGGCGCTGGCAGTAGAGAATGTGGCCTACTGTGACAGGGACCTCGTCCCTCATCTGTAAAACAATAACTAAGGATTCCT

Ensembl | mouse accession no.

NCBI accession no.

shipped in

ambient

storage temp.

−20°C

Gene Information

Related Categories

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

EMU154061-50UG:
EMU154061-20UG:


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S R Sennoune et al.
Cellular and molecular biology (Noisy-le-Grand, France), 61(7), 40-49 (2015-11-17)
Cytosolic Ca2+ ([Ca2+]cyt) is important in the regulation of several cellular functions involved in metastasis. We hypothesize that distinct [Ca2+]cyt regulation explains the acquisition of a more metastatic phenotype. To test this hypothesis, we used highly and lowly metastatic human

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