Millicell® Cell Culture Insert, 30 mm, hydrophilic PTFE, 0.4 µm PICM0RG50 from MilliporeSigma

Product Details
ItemMillicell® Cell Culture Insert, 30 mm, hydrophilic PTFE, 0.4 µm
CompanyMilliporeSigma
PriceSupplier Page
Catalog NumberPICM0RG50
Quantity50
ApplicationsCell Culture

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MilliporeSigma

6211 El Camino Real

Carlsbad, CA 92009

United States

Phone: +17607106100

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Website: sigmaaldrich.com/

(156) Stalk cell phenotype depends on integration of Notch and Smad1/5 signaling cascadesDevelopmental cellMarch 13, 2012Moya IM, Umans L, Maas E, Pereira PN, Beets K, Francis A, Sents W, Robertson EJ, Mummery CL, Huylebroeck D, et al.explanted and cultured. These dorsal explants were cultured on Millicell cell culture inserts (Millipore, PICM0RG50) in DMEM supplemented with 20% FBS and 50 μg/ml Endothelial Cell Growth Supplement (Millipore) in a

(157) Optimizing promoters for recombinant adeno-associated virus-mediated gene expression in the peripheral and central nervous system using self-complementary vectorsHuman gene therapySeptember 1, 2011Gray SJ, Foti SB, Schwartz JW, Bachaboina L, Taylor-Blake B, Coleman J, Ehlers MD, Zylka MJ, McCown TJ, Samulski RJ.Harvested tissue was sliced into 250-lm-thick sections, using a McIlwain tissue chopper, and plated on PICM0RG50 0.4-lm membranes (Millipore, Bedford, MA) with full complement medium. Slices were cultured for 7 days before

(158) UV-sensitive photoreceptor protein OPN5 in humans and micePloS oneJanuary 1, 2011Kojima D, Mori S, Torii M, Wada A, Morishita R, Fukada Y.thickness with a stainless razor blade. Each of the slices was put on the Millicell Standing Insert (PICM0RG50; Millipore, MA) set in a 35-mm dish, which was filled with 1.3 mL of the recording medium [D-MEM (Sigma)

(159) Circadian modulation of gene expression, but not glutamate uptake, in mouse and rat cortical astrocytesPloS oneOctober 15, 2009Beaulé C, Swanstrom A, Leone MJ, Herzog ED.Millicell-CM organotypic culture membrane placed on top of a Millicell insert (Millipore, 0.4 µm pore size, PICM0RG50). The insert was placed into a 35 mm sterile Petri dish (Falcon BD Biosciences, CA) containing 1 ml

(160) Modeling Neural Injury in Organotypic Cultures by Application of Inertia-Driven Shear StrainJournal of NeurotraumaJune 30, 2007Michael Bottlang, Mark B. Sommers, Theresa A. Lusardi, Jennifer J. Miesch, Roger P. Simon, Zhi-Gang Xiongentorhinal cortex, and then transferred to Millicell culture plate inserts with microporous membranes (PICM0RG50; Millipore, Bedford, MA; Fig. 1a). Inserts were preincubated in culture medium containing 50% MEM, 25%

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