3t3-l1 - OmicsDI

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Genomics (437)
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Mus musculus (385)
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Mass Spectrometry (47)
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Vanquish Flex Binary UHPLC coupled to a Thermo Scientific Orbitrap Exploris 240 high-resolution mass spectrometer (HRMS) (1)
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2017 (14)
2007 (12)
2006 (2)
2004 (2)
2005 (1)
2003 (1)

UNIPROT ID/AC

A1L347 (12)
A2A547 (12)
A2A5N2 (12)
A2A8V9 (12)
A2A9I0 (12)
A2AJ72 (12)
A2AL50 (12)
A2AL85 (12)
A2AVJ7 (12)
A3KML3 (12)
A6ZI44 (12)
A8IP69 (12)
B2MWM9 (12)
B2RRX1 (12)
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B7FAU9 (12)
B9EHN0 (12)
B9EIU1 (12)
D3YXK2 (12)
E9PUQ5 (12)
E9PVC5 (12)
E9PW20 (12)
E9PZF0 (12)
E9Q1G8 (12)
E9Q1P8 (12)
E9Q4Q2 (12)

ENSEMBL ID

ENSMUSG00000027651 (12)
ENSMUSP00000141097 (10)
ENSMUSG00000021039 (9)
ENSMUSG00000090272 (6)
ENSMUSP00000106991 (6)
ENSMUSP00000111587 (6)
ENSMUSG00000098557 (5)
ENSMUSP00000141542 (1)

CHEBI ID

CHEBI:15811 (2)
CHEBI:17200 (2)
CHEBI:44215 (2)
CHEBI:16171 (2)
CHEBI:17013 (2)
CHEBI:17256 (2)
CHEBI:15713 (2)
CHEBI:16264 (2)
CHEBI:17659 (2)
CHEBI:15414 (2)
CHEBI:16680 (2)
CHEBI:17202 (2)
CHEBI:16856 (2)
CHEBI:16238 (2)
CHEBI:48928 (2)
CHEBI:16695 (2)
CHEBI:16742 (2)
CHEBI:17562 (2)
CHEBI:16750 (2)
CHEBI:15428 (2)
CHEBI:16958 (2)
CHEBI:15741 (2)
CHEBI:16235 (2)
CHEBI:16335 (2)
CHEBI:15351 (2)
CHEBI:16108 (2)
CHEBI:15996 (2)
CHEBI:17552 (2)
CHEBI:15422 (2)
CHEBI:18012 (2)

Metabolite Name

Keto-D-fructose 6-phosphate (1)
3-sulfopyruvic acid (1)
Palmitoyl-CoA (1)
Keto-phenylpyruvate (1)
Menadione (1)
7H-purine (1)
Isocaproic acid (1)
N(2)-acetyl-L-lysine (1)
Beta-cellobiose (1)
NMN zwitterion (1)
Alpha-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-D-Glcp (1)
Thiamine(1+) diphosphate (1)
UDP-alpha-D-glucuronic acid (1)
2,3-bisphospho-D-glyceric acid (1)
Molybdate (1)
Alpha-D-galacturonic acid (1)
3-hydroxy-1-benzopyran-2-one (1)
3'-dephospho-CoA (1)
Geranyl diphosphate (1)
Isobutyryl-CoA (1)
N(omega),N(omega)-dimethyl-L-arginine (1)
4-hydroxy-3-methylbenzoic acid (1)
Taurodeoxycholic acid (1)
Ursodeoxycholic acid (1)
UTP (m+7) (1)
UTP (m+6) (1)
UTP (m+5) (1)
UTP (m+4) (1)
UTP (m+3) (1)
UTP (m+2) (1)

First Public Date

2014 (71)
2023 (43)
2025 (31)
2021 (29)
2026 (26)
2024 (25)
2022 (23)
2017 (23)
2019 (20)
2020 (19)
2018 (18)
2013 (16)
2015 (13)
2016 (6)
2012 (1)

Modification

N6-dimethyl-L-lysine (2)
N6 (1)

Study type

Transcription profiling by array (144)
ChIP-seq (34)
RNA-seq of coding RNA (20)
Comparative genomic hybridization by array (6)
ChIP-chip by tiling array (4)
ATAC-seq (4)
MicroRNA profiling by array (4)
Methylation profiling by array (4)
Transcription profiling by RT-PCR (3)
Other (3)
Methylation profiling by high throughput sequencing (3)
RNA-seq of total RNA (3)
Unknown experiment type (2)
RNAi profiling by array (2)
DNA-seq (2)
Animal - High-throughput sequencing (1)
Cell line - High-throughput sequencing (1)
Transcription profiling by tiling array (1)
ChIP-chip by array (1)
RNA-seq of coding RNA from single cells (1)
RNA-seq of non coding RNA (1)

Release Date

2022 (177)
2023 (147)
2021 (140)
2025 (137)
2019 (130)
2020 (117)
2018 (117)
2024 (107)
2016 (106)
2017 (98)
2015 (97)
2014 (78)
2013 (78)
2012 (66)
2010 (61)
2011 (55)
2008 (53)
2009 (41)
2007 (24)
2026 (23)
2006 (10)
2005 (7)
2003 (6)
2004 (5)
1999 (4)
2001 (2)
1998 (2)
2000 (1)
1983 (1)

Lab affiliation

Helmholtz-Centre for Environmental Research UFZ GmbH (6)
CIB-CSIC (Spanish Research Council) (2)
Charles Perkins Centre, School of Life and Environmental Sciences and Sydney Medical School, University of Sydney, Camperdown, NSW, Australia (2)
The Charles Perkins Centre School of Life and Environmental Sciences The University of Sydney Australia (2)
Weill Cornell Medicine-Qatar (2)
Amsterdam UMC location University of Amsterdam, Department of Medical Biochemistry, Amsterdam, the Netherlands. (1)
Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK. (1)
Boston University School of Medicine (1)
Cambridge Institute for Medical Research, University of Cambridge, Hills Road, Cambridge, CB2 0XY, UK (1)
Center for Bioanalysis, Korea Research Institute of Standards and Science (1)
Center for Network Systems Biology, Boston University School of Medicine, Boston, MA, United States. (1)
Central European Institute of Technology, Masaryk University, Brno, Czech Republic (1)
Copenhagen University (1)
Department of Biochemistry and Molecular Biology, University of Southern Denmark, 5230 Odense M, Denmark (1)
Department of Health Sciences, University “Magna Græcia” of Catanzaro, Viale Europa (Località Germaneto), 88100 Catanzaro, Italy (1)
Department of Immunology, College of Basic Medicine, Army Medical University (Third Military Medical University), Chongqing 400038, China. (1)
Department of Medicine/Division of Endocrinology, University of Arizona College of Medicine (1)
Department of Physical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland Proteomics and Mass Spectrometry Laboratory, Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland (1)
Department of Redox Molecular Medicine, Tohoku University Graduate School of Medicine (1)
Genomics Research Center, Academia Sinica (1)
Genomics Research Center, Academia Sinica, Taipei, Taiwan (1)
Institute of Metabolic Science, University of Cambridge, UK (1)
Institute of Molecular Medicine and Genetics,Shandong University, PR China (1)
Johns Hopkins University (1)
Maisonneuve-Rosemont Hospital Research Center and Department of Medicine, University of Montréal, Montréal H3C 3J7, Québec, Canada (1)
Max Planck Institute of Biochemistry, Martinsried, Germany (1)
Metabolomics-Proteomics Research Center, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan (1)
Proteomics and Metabolomics Unit, Monzino Cardiologic Center, IRCCS, Milan, Italy (1)
Proteomics program, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark (1)
Reader | Centre for Genomics and Computational Biology Barts Cancer Institute Queen Mary, University of London John Vane Science Centre, Charterhouse Square, London EC1M 6BQ Tel: +44 (0)20 7882 8266 (1)

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C13 Pyruvate Flux in 3t3 L1

Not available

ORGANISM(S): Mus musculus

ST000271 | MetabolomicsWorkbench

Genome-wide mapping of 5-hydroxymethylcytosine (5hmC) during differentiation of P19.6 and 3T3-L1 cells

Enhancers are developmentally-controlled transcriptional regulatory regions whose activities are modulated through histone modifications or histone variant deposition. Here, we show by genome-wide mapping that the newly discovered DNA modification 5-hydroxymethylcytosine (5hmC) is dynamically associ...

ORGANISM(S): Mus musculus

2012-06-04 | E-GEOD-38407 | biostudies-arrayexpress

Detection of microRNA expression during 3T3-L1 pre-adipocyte differentiation using a custom made microarray chip.

Differentiation of 3T3-L1 cells into adipocytes involves a highly orchestrated series of events including clonal expansion, growth arrest and terminal differentiation. The mechanisms coordinating these different steps are not yet fully understood. Here we investigated whether micro (mi)RNAs play a...

ORGANISM(S): Mus musculus

2010-05-18 | E-GEOD-16229 | biostudies-arrayexpress

Transcription profiling of mouse 3T3-L1 cells treated 24 hours with either 0.1% DMSO, 20uM pioglitazone, 1uM rosiglitazone or 20uM troglitazone

3T3-L1 cells treated 24 hours with either 0.1% DMSO, 20uM pioglitazone, 1uM rosiglitazone or 20uM troglitazone

ORGANISM(S): Mus musculus

2007-10-09 | E-GEOD-1458 | biostudies-arrayexpress

Expression data from Fbxl10 overexpressing 3T3-L1 cells

Target genes of Fbxl10 during 3T3-L1 adipogenesis was analyzed 3T3-L1 cells overexpressing Fbxl10 using retrovirus system containing LTR promoter were differentiated and RNA was extracted at day 2 of differentiation

ORGANISM(S): Mus musculus

2015-03-04 | E-GEOD-64154 | biostudies-arrayexpress

Genome-wide RING1B binding in Fbxl10 overexpressing 3T3-L1 cells at day 2 of differentiation

We analyzed RING1B binding regions in 3T3-L1 cell lines transduced with the retroviral vector for V5-tagged Fbxl10 or its dF-box mutant. RING1B ChIP-seq in empty, Fbxl10-1, and dF-box mutant vector transduced 3T3-L1 preadipocytes, in duplicate, and V5-Fbxl10 ChIP-seq in Fbxl10 overexpressing 3T3-L1 ...

ORGANISM(S): Mus musculus

2015-03-04 | E-GEOD-64312 | biostudies-arrayexpress

RNAi knockdown of Tip60 and Usp7 in mouse 3T3-L1 adipocytes

Knockdown of Tip60 or Usp7 in differentiated 3T3-L1 adipocytes

ORGANISM(S): Mus musculus

2013-08-28 | E-TABM-1145 | biostudies-arrayexpress

MicroRNA profiling of mouse 3T3-L1 cells before and after adipogenesis

Compare miRNA expression profiles between undifferentiated 3T3-L1 preadipocytes (Day 0) and differentiated 3T3-L1 adipocytes (Day 9)

ORGANISM(S): Mus musculus

2009-02-19 | E-MEXP-1930 | biostudies-arrayexpress

Mechanistic analysis of the model obesogen Tributyltin in the 3T3-L1 cell line

Obesogenic compounds are chemicals that might have an influence on obesity development through in utero or chronic lifetime exposure. Tributyltin (TBT) is one of the most studied obesogenic compounds, inducing adipogenesis in vitro and increasing body fat after in utero exposure of mice. This study ...

ORGANISM(S): Mus musculus

2013-02-25 | E-GEOD-41340 | biostudies-arrayexpress

Transcription profiling of adult C57BL6 mouse tissues and 3T3-L1 fibroblasts

This SuperSeries is composed of the following subset Series:; GSE6793: Expression data from select tissues harvested from C57BL6 mice; GSE6794: Expression data from 3T3-L1 adipogenesis Experiment Overall Design: Refer to individual Series

Note: GSM156880.CEL is not available from GEO.

ORGANISM(S): Mus musculus

2007-11-06 | E-GEOD-6795 | biostudies-arrayexpress

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