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Merck
CN

EHU061721

MISSION® esiRNA

targeting human ZNF207

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NACRES:
NA.51
UNSPSC Code:
41105324

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产品名称

MISSION® esiRNA, targeting human ZNF207

description

Powered by Eupheria Biotech

product line

MISSION®

form

lyophilized powder

esiRNA cDNA target sequence

AAGGTGGCCGTTACTGATCTTACTTCATCCAGTCTAATAGGTTTGGAGATTAAACCTTTTCTCAACTTGTGCTGTTTATATAGCCAAGCTTCCGTCAATAAGGCTTCATTGTGACTTTAACAAACATTATCTTCCCACATACCAGGAACTATTGGACATTTATTTTACATGGGAAAAATTATTTGGAATAATAAAGCAGGAACTTTTCCTGAAGTTGCAATTTATACTGTATGGCTTCTTTTTCATGTTTCATCTAGGTTTTTAGAAGTGAAGTATAGTAAATTTGGTTCGTTAAATTGTGAAGGCGCTGGAATTACATGAACATACCACCCTAGTAAAGGCAAGTTCTGTAAGCTTACATTGCTATTTGTAAAGTTTGCCTTCACAGCATTTCAGATGCTGTTGGACTTCATGTCC

Ensembl | human accession no.

ENSG00000010244

NCBI accession no.

NM_001098507

shipped in

ambient

storage temp.

−20°C

Quality Level

100

Gene Information

human ... ZNF207(7756), ZNF207(7756)

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

存储类别

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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Yuejia Huang et al.
The Journal of cell biology, 217(1), 107-116 (2017-10-28)
Protein phase separation or coacervation has emerged as a potential mechanism to regulate biological functions. We have shown that coacervation of a mostly unstructured protein, BuGZ, promotes assembly of spindle and its matrix. BuGZ in the spindle matrix binds and
Joseph Dopie et al.
The Journal of cell biology, 219(9) (2020-07-02)
We present a simple ratio method to infer protein composition within cellular structures using proximity labeling approaches but compensating for the diffusion of free radicals. We used tyramide signal amplification (TSA) and label-free mass spectrometry (MS) to compare proteins in

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