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EMU081121

Sigma-Aldrich

MISSION® esiRNA

targeting mouse Pthlh

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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

AAACCAACAAGGTGGAGACGTACAAAGAACAGCCACTCAAGACACCCGGGAAGAAGAAGAAAGGCAAGCCTGGGAAACGCAGAGAACAGGAGAAAAAGAAGCGAAGGACTCGGTCTGCCTGGCCAAGCACAGCTGCGAGTGGCCTGCTTGAGGACCCCCTGCCCCACACCTCCAGGACCTCGCTGGAGCCCAGCTTAAGGACGCATTGAAATTTTCATCGAAGATCTTCCAAGGACACGTTACAGGATTTTGTAATAGTAAACATATGGAAAGTATTAGACATATTTATTGCCTGTACATACTGTAAATGCATTGGGATCAAACTGTCTCCCCAGGAAACTGCACATGGGTCATGTGAATATTTTTCCCTTTTGCCAAGGCTAATCCAATTATTCCTGTCACTGTTACCATAATTTATTTTGTCAACTGATGTATTTATTTGTAAATGTATCTTGGTGCTGCTGACTCTG

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


Certificates of Analysis (COA)

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Jen-Yu Hung et al.
International journal of oncology, 46(5), 1985-1993 (2015-03-05)
This is the first study to demonstrate that benzo(a)-pyrene (BaP) was able to enhance the production of parathyroid hormone‑related protein (PTHrP) by human non‑small cell lung cancer H460 cells. Such effect would further contribute to bone metastasis of lung cancer
María Mar Roca-Rodríguez et al.
The Journal of clinical endocrinology and metabolism, 100(6), E826-E835 (2015-04-18)
This study aimed to define the potential role of PTHrP on adipogenic regulation and to analyze its relationship with obesity and insulin resistance. This was a cross-sectional study in which visceral (VAT) and subcutaneous (SAT) adipose tissue were extracted from

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