3T3-L1 Differentiation Medium, 100ml from Zen-Bio, Inc.

Product Specs
Item3T3-L1 Differentiation Medium, 100ml
CompanyZen-Bio, Inc.
Price Pricing Info Supplier Page View Company Product Page
Catalog NumberDM-2-L1
Quantity100ml
Temperature4C
TypeMEDIA

Add to Compare List

Zen-Bio, Inc.

3920 South Alston Ave

Durham, North Carolina 27713

United States

Phone: (866)234-7673 or (919)547-0692
(919)547-0693

Company Profile

Website: http://www.zen-bio.com

(1) Anti-Adipogenic Activity of Secondary Metabolites Isolated from Smilax sieboldii Miq. on 3T3-L1 AdipocytesInternational Journal of Molecular SciencesMay 16, 2023Yeon Woo Jung, Jung A Lee, Ji Eun Lee, Hanna Cha, Yun-Hyeok Choi, Wonsik Jeong, Chun Whan Choi, Joa Sub Oh, Eun-Kyung Ahn, Seong Su Hongmedia [3T3-L1 Differentiation Medium (3-isobutyl-1-methylxanthine, dexamethasone, and insulin (MDI)); DM-2-L1, Zenbio] was performed. The initiation medium was changed on day two with the 3T3-L1 Adipocyte Medium

(2) Investigation on the Biological Safety and Activity of a Gluconolactone-Based Lotion for Dermocosmetic ApplicationPharmaceuticals (Basel)April 27, 2023Nicola Zerbinati, Serena Di Francesco, Maria Chiara Capillo, Cristina Maccario, Giorgio Stabile, Hassan Galadari, Raffaele Rauso, Sabrina Sommatis, Roberto MocchiUSA); two days after reaching confluence, the culture medium was switched to differentiation medium (DM-2-L1, Zen-Bio, Durham, NC, USA) for 3 days at 37 °C. Then, cells were maintained in maintenance medium (AM-1-L1,

(3) Tumor-derived IL-6 and trans-signaling among tumor, fat, and muscle mediate pancreatic cancer cachexiaThe Journal of experimental medicineJune 7, 2021Rupert JE, Narasimhan A, Jengelley DHA, Jiang Y, Liu J, Au E, Silverman LM, Sandusky G, Bonetto A, Cao S, et al.ensure growth arrest, refreshing the preadipocyte media every 48 h. Cells were then washed with PBS, DM (DM-2-L1; Zen Bio) was added to the wells, and the cells were placed back into the incubator. Cells were cultured

(4) GRIM19 Impedes Obesity by Regulating Inflammatory White Fat Browning and Promoting Th17/Treg BalanceCellsJanuary 15, 2021Jhun J, Woo JS, Lee SH, Jeong JH, Jung K, Hur W, Lee SY, Ryu JY, Moon YM, Jung YJ, et al.Subsequently, the cells were incubated in an appropriate volume of 3T3-L1 cell differentiation medium (DM2-L1, ZenBio) for 3 days, followed by incubation with 3T3-L1 adipocyte maintenance medium (AM-1-L1, ZenBio).

(5) Screening and Identification of an Anti-inflammatory and Anti-adipogenic Constituent from Ligularia taquetii NakaiNatural Product CommunicationsJanuary 1, 2020Sungchan Jang, Min-Seon Kim, Taejin Park, Ji H. Sim, Seung-Young Kimof LTE and CGA, the culture medium was then replaced with 3T3-L1 Differentiation Medium (Cat. no. DM-2-L1, ZenBio, Research Triangle Park, United States) containing LTE and a 0.1% v/v DMSO vehicle. After 72

(6) Biphasic Effect of Sildenafil on Energy Sensing is Mediated by Phosphodiesterases 2 and 3 in Adipocytes and HepatocytesInternational Journal of Molecular SciencesJune 19, 2019Jheelam Banerjee, Antje Bruckbauer, Teresa Thorpe, Michael B. Zemelair. Confluent pre-adipocytes were induced to differentiate with a standard differentiation medium (DM2-L1, Zen-Bio Inc., Research Triangle Park, NC, USA). Pre-adipocytes were maintained in this differentiation

(7) Adipocyte-Derived Lipids Mediate Melanoma Progression via FATP ProteinsCancer DiscoveryAugust 1, 2018Maomao Zhang et al.no. PM-1-L1). 2 days post confluency, media was changed to differentiation medium (ZenBio, Cat no. DM-2-L1) and incubated for 5 days. Then, cells were maintained in their adipocytic, differentiated state with

(8) MicroRNA-30 modulates metabolic inflammation by regulating Notch signaling in adipose tissue macrophagesInternational journal of obesity (2005)June 1, 2018Miranda K, Yang X, Bam M, Murphy EA, Nagarkatti PS, Nagarkatti M.medium, differentiation medium, and adipocyte maintenance medium were also used (Zen-Bio, PM-1-L1, DM-2-L1, AM-1-L1). Conditioned medium was collected between days 7 and 14 post-differentiation, 0.22um filtered,

(9) The Effect of Pericellular Oxygen Levels on Proteomic Profile and Lipogenesis in 3T3-L1 Differentiated Preadipocytes Cultured on Gas-Permeable CulturewarePLOS ONEMarch 29, 2016Martin Weiszenstein, Nela Pavlikova, Moustafa Elkalaf, Petr Halada, Ondrej Seda, Jan Trnka, Jan Kovar, Jan PolakProteomic Profile on Gas-Permeable Cultureware culture medium was changed to differentiation medium (DM2-L1, Zen-Bio Inc., NC, USA) and cells were placed in sealed plastic chambers—modular incubators (Billups-Rothenberg, CA,

(10) Role of Micro RNA-205 in Promoting Visceral Adiposity of NZ10 Mice with Polygenic Susceptibility for Type 2 DiabetesJournal of Diabetes & MetabolismDecember 15, 2015Nikhil Adi, Jennipher Adi, Liliana Cesar, Paul Kurlansky, Arthur Agatston, Keith A Websterto 100% confluency and after 2 days the media was replaced with adipogenic differentiation medium (DM-2-L1, Zen-Bio). After 3 days the DM-2-L1 media was replaced by adipocyte maintenance medium (AM-1-L1, Zen-Bio).

(11) Interaction between leucine and phosphodiesterase 5 inhibition in modulating insulin sensitivity and lipid metabolismDiabetes, Metabolic Syndrome and Obesity: Targets and TherapyMay 23, 2015Michael Zemel, Fenfen Fu, Fenfen Bruckbauer, Antje Bruckbauer, Qiang Cao, Rui Wu, Hang Shi, Bingzhong Xue, Michael B Zemelair. Confluent preadipocytes were induced to differentiate with a standard differentiation medium (DM2-L1; Zen-Bio Inc., Research Triangle Park, NC, USA). Preadipocytes were maintained in this differentiation

(12) Macrophage Elastase Suppresses White Adipose Tissue Expansion with Cigarette SmokingAmerican Journal of Respiratory Cell and Molecular BiologyDecember 1, 2014Takao Tsuji, Neil J. Kelly, Saeko Takahashi, Adriana S. Leme, A McGarry McGarry Houghton, Steven D. Shapiroobtained from Zen-Bio, Inc. (Durham, NC). Cells were incubated for 2 days in PM-1-L1 (Zen-Bio), moved to DM-2-L1 (Zen-Bio), and incubated for 3 days. Differentiated adipocytes were maintained in AM-1-L1 (Zen-Bio).

(13) Capsaicin Induces “Brite” Phenotype in Differentiating 3T3-L1 PreadipocytesPLoS ONEJuly 29, 2014Ritesh K. Baboota, Dhirendra P. Singh, Siddhartha M. Sarma, Jaspreet Kaur, Rajat Sandhir, Ravneet K. Boparai, Kanthi K. Kondepudi, Mahendra BishnoiTriangle Park, NC). Dulbecco's modified Eagle's medium (DMEM), 3T3-L1 adipocyte differentiation media (DM-2-L1) and 3T3-L1 adipocyte maintenance media (AM-1-L1) were obtained from Zenbio Inc. (Research Triangle

(14) Synergistic Effects of Polyphenols and Methylxanthines with Leucine on AMPK/Sirtuin-Mediated Metabolism in Muscle Cells and AdipocytesPLoS ONEFebruary 14, 2014Antje Bruckbauer, Michael B. Zemelair. Confluent pre-adipocytes were induced to differentiate with a standard differentiation medium (DM2-L1, Zen-Bio Inc., NC). Pre-adipocytes were maintained in this differentiation medium for 3 days and subsequently

(15) Synergistic effects of metformin, resveratrol, and hydroxymethylbutyrate on insulin sensitivityDiabetes, Metabolic Syndrome and Obesity: Targets and TherapyFebruary 23, 2013Michael Bruckbauer, Michael B Bruckbaueratmosphere. Confluent preadipocytes were induced to differentiate using a standard differentiation medium (DM2L1, Zen-Bio Inc, Research Triangle Park, NC, USA). The preadipocytes were maintained in this differentiation

(16) Mechanisms of Adipocytokine-Mediated Trastuzumab Resistance in HER2-Positive Breast Cancer Cell LinesCurr Pharmacogenomics Person MedJanuary 17, 2013Samantha E Griner, Katherine J Wang, Jayashree P Joshi, Rita Nahtafor days 0 through 6 (Fig. (1A)). During days 6 to 9, cells were cultured in Differentiation Medium (DM-2-L1; Zen-Bio), which contains isobutylmethylxanthine and a PPARy agonist. Differentiation was confirmed

(17) Hkat, a novel nutritionally regulated transmembrane protein in adipose tissuesScientific ReportsDecember 21, 2012Ren Zhangpreadipocyte medium (Catalog number PM-1-L1, Zenbio, Research Triangle Park, NC), differentiation medium (DM-2-L1) and adipocyte maintenance medium (AM-1-L1). Briefly, 3T3 L1 cells was allowed to reach confluence in

(18) Inositol Pyrophosphates Inhibit Akt Signaling, Thereby Regulating Insulin Sensitivity and Weight GainCellDecember 10, 2010Anutosh Chakraborty et al.were maintained in preadipocyte media (PM-1-L1), differentiated for 3 days with differentiation media (DM-2-L1). After 3 days of differentiation, cells were maintained for another 7 days in adipocyte maintenance

Be the First to Write a Review!

Interview with Ed Anderson from ASHG 2019
In this interview, Ed Anderson discusses his poster at ASHG 2019 entitled, "Development of a haploid... Read More

3T3-L1 Differentiation Medium, 100ml from Zen-Bio, Inc.

Zen-Bio, Inc.

Citations (18)

Reviews

Videos

Interview with Ed Anderson from ASHG 2019

3T3-L1 Differentiation Medium, 100ml from Zen-Bio, Inc.

About Biocompare

Advertise with Us

Specialized Search Tools

Site Map