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EHU017371

Sigma-Aldrich

MISSION® esiRNA

targeting human ZBTB5

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100 MG
$306.00

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100 MG
$306.00

About This Item

UNSPSC Code:
41105324
NACRES:
NA.51

$306.00


Please contact Customer Service for Availability

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description

Powered by Eupheria Biotech

Quality Level

product line

MISSION®

form

lyophilized powder

esiRNA cDNA target sequence

TGAATGGAGCTACGTCCTCATTTGAAAATGGCCATCCTTCCCAGCCTGGCCCTCCACAGTTGACCAGGGCATCTGCAGATGTTCTGTCAAAGTGCAAGAAGGCCTTATCAGAGCACAATGTTTTGGTTGTAGAGGGAGCTCGCAAGTATGCCTGCAAAATCTGCTGCAAAACTTTTCTGACTTTGACAGATTGCAAGAAGCACATCCGTGTTCACACAGGTGAAAAGCCTTACGCCTGCCTGAAGTGTGGCAAGAGGTTTAGTCAGTCCAGCCACCTGTATAAGCACTCAAAGACTACCTGCCTGCGCTGGCAGAGCAGCAATCTTCCCAGCACTTTGCTCTAGCTGTTTGTCCTTACAAGACAACGCTGAGGCCAGTTGTCAGACTGAATTTCTTTTGGTAAGCAGTTAATGCCTTTGGGTTCGA

Ensembl | human 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

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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A Karipides et al.
Acta crystallographica. Section C, Crystal structure communications, 45 ( Pt 11), 1743-1745 (1989-11-15)
C18F15P, Mr = 532.1, monoclinic, P2(1)/c, a = 7.194 (2), b = 17.930 (4), c = 13.834 (2) A, beta = 94.29 (2) degrees, V = 1779 A3, Z = 4, Dm = 2.00, Dx = 1.99 g cm-3, lambda(Mo
Barbara Chiavarino et al.
European journal of mass spectrometry (Chichester, England), 16(3), 407-414 (2008-01-01)
Functional models of the Compound I intermediate of monooxygenase heme enzymes, namely [(TPFPP)(*+)Fe(IV)=O](+) and [(TPFPP)Mn(V)=O](+) (TPFPP = meso-tetrakis (pentafluorophenyl)porphyrinato dianion), are obtained as bare species by electrospray ionization from solutions of appropriate precursors and their reactivity is investigated in the
Rui Zhang et al.
Journal of the American Chemical Society, 127(18), 6573-6582 (2005-05-05)
Porphyrin-manganese(V)-oxo and porphyrin-manganese(IV)-oxo species were produced in organic solvents by laser flash photolysis (LFP) of the corresponding porphyrin-manganese(III) perchlorate and chlorate complexes, respectively, permitting direct kinetic studies. The porphyrin systems studied were 5,10,15,20-tetraphenylporphyrin (TPP), 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin (TPFPP), and 5,10,15,20-tetrakis(4-methylpyridinium)porphyrin (TMPyP). The

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