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siRNA Universal Neg. Controls

All ordering options are in the Available siRNA Universal Negative Controls table.

MISSION® siRNA Universal Negative Controls are an essential component of any gene silencing experiment. The negative controls have been designed to distinguish sequence-specific silencing from non-specific effects.

Product Benefits

  • No homology to any known gene sequence
  • Available with fluorescent labels, thereby allowing rapid assessment of transfection efficiency
  • Tested in vitro in Human, Mouse & Rat cells

Product Features

  • Options: 2 unique sequences available unmodified & modified
  • Quantities: 0.2 (1 nmol), 5 x 0.2 (5 x 1 nmol) & 5 (10 nmol) OD
  • Purification: Desalt
  • Sequence Form: 21mer duplexes with dTdT overhangs
  • Modifications: Cyanine 3, Cyanine 5 & 6-FAM available
  • Quality Control: 100% mass spectrometry*
  • Format: Supplied dry in tubes

*Depending on manufacturing site, PAGE may be used to assess siRNA duplexes.

Customization of the above features are available. For feasibility review of your specific needs, please send a request to sirnarequest@sial.com.

Available siRNA Universal Negative Controls
Product No.Product NameDescriptionPricing
OGS207PSF-OXB20-BETAGAL - BACTERIAL BETA GALACTOSIDASE PLASMIDplasmid vector for molecular cloning
OGS412PSF-OXB20-FLUC - BACTERIAL LUCIFERASE PLASMIDplasmid vector for molecular cloning
OGS50PSF-OXB20 - STRONG BACTERIAL PROMOTER PLASMIDplasmid vector for molecular cloning
OGS553PSF-OXB1 - WEAK STRENGTH BACTERIAL PROMOTER PLASMIDplasmid vector for molecular cloning
OGS500PSF-T7/LACO - T7 LACO INDUCIBLE BACTERIAL PLASMIDplasmid vector for molecular cloning
OGS501PSF-TAC - PTAC INDUCIBLE BACTERIAL PLASMIDplasmid vector for molecular cloning
OGS502PSF-LACI - LACI PROMOTER BACTERIAL VECTORplasmid vector for molecular cloning
OGS388PSF-CMV-PGK-FLUC - DUAL PROMOTER LUCIFERASE PLASMIDplasmid vector for molecular cloning
OGS103PSF-CMV-RLUC - CMV RENILLA LUCIFERASE PLASMIDplasmid vector for molecular cloning
OGS10PSF-CMV-KAN - KANAMYCIN RESISTANCE PLASMIDplasmid vector for molecular cloning
OGS505PSF-CAG-KAN - CAG PROMOTER VECTORplasmid vector for molecular cloning
OGS43PSF-EF1 ALPHA - ELONGATION FACTOR ALPHA PROMOTER PLASMIDplasmid vector for molecular cloning
OGS394PSF-CMV-PGK-PURO - DUAL PROMOTER PUROMYCIN PLASMIDplasmid vector for molecular cloning
OGS588PSF-CMV-BLAST - CMV PROMOTER BLASTICIDIN RESISTANT PLASMIDplasmid vector for molecular cloning
OGS22PSF-CMV-UB-NEO/G418 ASCI - G418 SELECTION PLASMIDplasmid vector for molecular cloning
OGS1157PSF-CMV-PURO-NH2-10HIS-EKT - N-TERMINAL 10HIS TAG MAMMALIAN PLASMIDplasmid vector for molecular cloning
OGS1175PSF-CMV-PURO-NH2-FLAG®-6HIS-EKT - N-TERMINAL FLAG® AND 6 HIS DUAL TAG MAMMALIAN PLASMIDplasmid vector for molecular cloning
OGS1120PSF-CMV-PURO-COOH-TEV-10HIS - C-TERMINAL 10HIS TAG MAMMALIAN PLASMIDplasmid vector for molecular cloning

Validation Data

HeLa cells were seeded in 24-well plates 24 hours prior to transfection at a density of 40,000 cells per well. Cells were then transfected using the MISSION siRNA Transfection Reagent and 10 nM of the various Fluorescent Universal Negative Controls. Fluorescence was assessed 24 hours post-transfection, and images were captured at 40X magnification. Figure 1 shows examples of treatment cells with expected results. Figure 2 shows control cells with no Fluorescent Universal Negative Controls present.

Microscopic images of treatment cells.

Figure 1.Microscopic images of treatment cells. A) DIC (differential interference contrast) and fluorescence microscopy of SIC003 Fluorescent Universal Negative Control #1 w/Cyanine 3 (excitation: 550 nm & emission: 570 nm; RFP filter excitation: 555 nm ±25 & detection: 605 nm ±52) B) DIC and fluorescence microscopy of SIC005 Fluorescent Universal Negative Control #1 w/Cyanine 5 (excitation: 650 nm & emission: 670 nm; Cyanine 5 filter excitation: 320 nm ±60 & detection: 700 nm ±75) and C) DIC and Fluorescence microscopy of Fluorescent SIC007 Universal Negative Control #1 w/6-FAM (excitation: 495 nm & emission: 516 nm; GFP filter excitation: 490 nm ±20 & detection: 525 nm ±36). Arrows indicate a cell where fluorescence is evident.

Microscopic images of control cells (treated only with transfection reagent).

Figure 2.Microscopic images of control cells (treated only with transfection reagent). A) DIC B) Fluorescent Cyanine 5 filter C) Fluorescent GFP filter and D) Fluorescent RFP filter. Some autofluorescence is visible. However, it is very dim compared to the Fluorescent Universal Negative Controls w/Cyanine 3, Cyanine 5 & 6-FAM.

If additional help is needed, please consult our technical services group at oligotechserv@sial.com.

MISSION is a trademark of Merck KGaA, Darmstadt, Germany, and/or its affiliates. Label License.

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