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Upgrade your cell culture today
Culture cells with Advanced media
Consistent cell growth, less serum, lower costEnriched with normal-serum constituents, Gibco™ Advanced™ media can be used in combination with your fetal bovine serum (FBS), and feature:
• Formulations that support common cell lines (e.g., Advanced DMEM, DMEM/F-12, MEM, RPMI 1640)
• Fewer lot-to-lot changes of serum, which means less variability
• Reduced cost due to lower serum usage and fewer lots tested
• Equivalent cell growth/no change in morphology of common cell lines (Figure 1)
Culture cells with GlutaMAX media
More stable than L-glutamine —keeping your cells healthier for longerL-glutamine can degrade in culture media to form toxic ammonia, which decreases cell viability. Gibco™ GlutaMAX™ Supplement, on the other hand, is a stabilized form of L-glutamine, and features:
• Superior stability—helps prevent degradation during storage or in the presence of cells, which happens with L-glutamine (Figure 2)
• Flexibility—available as a stand-alone supplement or as a component in Gibco™ basal media products
Figure 1. Growth of cell lines in Advanced media.
Figure 2. Stability of Gibco™ CTS™ GlutaMAX™-I Supplement vs. L-glutamine in DMEM. DMEM was supplemented with GlutaMAX-I or L-glutamine, aliquotted into vials, and stored at 37°C. Samples were taken daily and frozen at –20°C. Levels of GlutaMAX-I supplement and L-glutamine were determined by high-performance liquid chromatography (HPLC).
Con
cent
ratio
n (m
g/L)
Time (days)
0 1 2 3 4 5 6 7
1,000
800
600
400
200
0
L-glutamine
GlutaMAX-I
18
16
14
12
10
8
6
4
2
0 Jurkat Vero SP2
Control: RPMI 1640 + 5% FBSAdvanced RPMI + 5% FBSAdvanced RPMI + 2% FBSAdvanced RPMI + 0.5% FBS
Cell line
Ave
rage
cel
ls/2
4-w
ell p
late
(x 1
05 )
A B
Detach cells with TrypLE Express
Cell detachment that is gentle on cell surface proteinsGibco™ TrypLE™ reagents are highly purifi ed, recombinant cell-dissociation enzymes that replace porcine trypsin. These reagents are ideal for dissociating attachment-dependent cell lines in both serum-containing and serum-free conditions. They can directly substitute for trypsin without protocol changes, and are:
• Stable at room temperature—no need to thaw
• Gentle on cells—help protect your cells’ surface proteins (Figure 3)
• Animal origin–free—important if you need a product without animal-derived components
Figure 3. Comparison of cell dissociation reagents. Jurkat cells were used to demonstrate the effects of cell dissociation reagents on detection of the cell surface epitope CD2. (A) Time course of treatment with Gibco™ TrypLE™ Express Enzyme (1X). There is no reduction in the CD2 fl uorescence signal. (B) Time course of treatment with 0.05% trypsin-EDTA. There is a time-dependent reduction in CD2 detection.
Figure 4. Fluorescence of PBS, FluoroBrite DMEM, and phenol red–free DMEM at 509 nm (excitation at 480 nm).
Sig
nal-
to-n
oise
rat
io o
f dex
tran
, A
lexa
Flu
or™
488
con
juga
te
PBS FluoroBriteDMEM
DMEM PBS FluoroBriteDMEM
DMEM
Bac
kgro
und
�uo
resc
ence
(480
nm
exc
itatio
n)
20,000
0
40,000
60,000
80,000
20
10
30
50
60
70
100
0
40
110
80
90
Image cells with FluoroBrite DMEM
Reduces background fl uorescence in cell imaging while preserving cell viability
Gibco™ FluoroBrite™ DMEM is a culture medium designed for imaging cells, and features:
• Background autofl uorescence 90% lower than the phenol red–free DMEM equivalent (Figure 4)
• Improved signal-to-noise ratio compared to the phenol red–free DMEM equivalent
Cou
nt
100 101 102 103 104
FL4-H :: CD2 APC
TrypLE 20 minTrypLE 15 minTrypLE 10 minTrypLE 5 minTrypLE 1 minControl
Sample ID
Cou
nt
100 101 102 103 104
FL4-H :: CD2 APC
0.05% Trypsin 20 min0.05% Trypsin 15 min0.05% Trypsin 10 min0.05% Trypsin 5 min0.05% Trypsin 1 minControl
Sample ID
Figure 5. Comparison of Gibco™ Recovery™ Cell Culture Freezing Medium vs. other cryopreservation technologies. For each cell line, the same number of cells were frozen in liquid nitrogen. Upon thawing, each cell sample was diluted into the same volume of a growth medium and seeded in 12-well plates (recovery was tested in eight different growth media). When the leading condition for a particular cell line had reached late log growth and none of the other conditions from that cell line had passed peak density, cells growing in all conditions for that cell line were harvested and the data analyzed. These cell lines were analyzed on day 6. Results were normalized to Gibco Recovery Cell Culture Freezing Medium and plotted with standard error bars (n = 4).
110100
908070605040302010
0CHO HeLa
Gibco (Cat. No. 12648-010)Sigma-Aldrich (Cat. No. C6164)Sigma-Aldrich (Cat. No. C6039)ScienCell (Cat. No. 0133)Cambrex (Cat. No. 12-132A)EMD Millipore (Cat. No. S-002-D)Growth medium (with 7.5% DMSO)BioLife Solutions (Cat. No. 99-640-DV)
Cell line
Cel
l rec
ove
ry (%
)(n
orm
aliz
ed to
Rec
over
y m
ediu
m)
1101009080706050403020100
CHO HeLa
Gibco (Cat. No. 12648-010)Sigma-Aldrich (Cat. No. C6164)Sigma-Aldrich (Cat. No. C6039)ScienCell (Cat. No. 0133)Cambrex (Cat. No. 12-132A)EMD Millipore (Cat. No. S-002-D)Growth medium (with 7.5% DMSO)BioLife Solutions (Cat. No. 99-640-DV)
Cell line
Cel
l rec
ove
ry (%
)(n
orm
aliz
ed to
Rec
over
y m
ediu
m)
Freeze cells with Recovery Freezing Medium
A complete, ready-to-use freezing medium for a wide variety of commonly used mammalian cell lines• No need to combine multiple products each time to make a home-brew freezing solution
• Improved viability of cells after thawing from cryostorage (Figure 5)
Find your upgrade product at thermofisher.com
For Research Use Only. Not for use in diagnostic procedures. © 2016 Thermo Fisher Scientific Inc. All rights reserved. All trademarks are the property of Thermo Fisher Scientific and its subsidiaries unless otherwise specified. Sigma-Aldrich is a registered trademark of Sigma-Aldrich Co. LLC. EMD Millipore is a trademark of MERCK. Cambrex is a trademark of Cambrex Corporation. ScienCell Research Laboratories is a trademark of ScienCell Research Laboratories, Inc. BioLife Solutions is a trademark of BioLife Solutions Inc. CO021199 0116