dialyzed fbs (Thermo Fisher)

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RPMI 1640 Medium no glutamine

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RPMI 1640 Medium was originally developed to culture human leukemic cells in suspension and as a monolayer Roswell Park Memorial Institute RPMI 1640 Medium has since been found suitable for a variety of mammalian cells including HeLa Jurkat MCF 7 PC12 PBMC astrocytes and carcinomas We offer a variety of RPMI 1640 Medium modifications for a range of cell culture applications Find the right formulation using the media selector tool This RPMI is modified as follows WithWithout• Phenol Red• HEPES• L glutamineThe complete formulation is available Using RPMIRPMI 1640 Medium is unique from other media because it contains the reducing agent glutathione and high concentrations of vitamins RPMI 1640 Medium contains biotin vitamin B12 and PABA which are not found in Eagle s Minimal Essential Medium or Dulbecco s Modified Eagle Medium In addition the vitamins inositol and choline are present in very high concentrations RPMI 1640 Medium contains no proteins lipids or growth factors Therefore RPMI 1640 Medium requires supplementation commonly with 10 Fetal Bovine Serum FBS RPMI 1640 Medium uses a sodium bicarbonate buffer system 2 0 g L and therefore requires a 5 10 CO2 environment to maintain physiological pH Product intended useFor in vitro diagnostic use CAUTION Not for human or animal therapeutic use Uses other than the intended use may be a violation of local law Customers using Gibco RPMI 1640 in a manufacturing process who have a submission with the FDA may request a letter of authorization from us to reference our Type II Drug Master File DMF cGMP manufacturing and quality systemRPMI 1640 Medium is manufactured at a cGMP compliant facility located in Grand Island New York The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards For supply chain continuity we offer an identical RPMI 1640 product made in our Scotland facility 31870 025 This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard

Catalog Number:

21870076

Price:

None

Category:

Cell Culture Transfection Reagents

Applications:

Cell Culture|Mammalian Cell Culture

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Thermo Fisher dialyzed fbs
RPMI 1640 Medium was originally developed to culture human leukemic cells in suspension and as a monolayer Roswell Park Memorial Institute RPMI 1640 Medium has since been found suitable for a variety of mammalian cells including HeLa Jurkat MCF 7 PC12 PBMC astrocytes and carcinomas We offer a variety of RPMI 1640 Medium modifications for a range of cell culture applications Find the right formulation using the media selector tool This RPMI is modified as follows WithWithout• Phenol Red• HEPES• L glutamineThe complete formulation is available Using RPMIRPMI 1640 Medium is unique from other media because it contains the reducing agent glutathione and high concentrations of vitamins RPMI 1640 Medium contains biotin vitamin B12 and PABA which are not found in Eagle s Minimal Essential Medium or Dulbecco s Modified Eagle Medium In addition the vitamins inositol and choline are present in very high concentrations RPMI 1640 Medium contains no proteins lipids or growth factors Therefore RPMI 1640 Medium requires supplementation commonly with 10 Fetal Bovine Serum FBS RPMI 1640 Medium uses a sodium bicarbonate buffer system 2 0 g L and therefore requires a 5 10 CO2 environment to maintain physiological pH Product intended useFor in vitro diagnostic use CAUTION Not for human or animal therapeutic use Uses other than the intended use may be a violation of local law Customers using Gibco RPMI 1640 in a manufacturing process who have a submission with the FDA may request a letter of authorization from us to reference our Type II Drug Master File DMF cGMP manufacturing and quality systemRPMI 1640 Medium is manufactured at a cGMP compliant facility located in Grand Island New York The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards For supply chain continuity we offer an identical RPMI 1640 product made in our Scotland facility 31870 025 This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard
https://www.bioz.com/result/dialyzed fbs/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
Price from $9.99 to $1999.99

dialyzed fbs - by Bioz Stars, 2021-03

99/100 stars

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Multiple Displacement Amplification:

Article Title: A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
Article Snippet: .. Reagents RPMI 1640 medium for 4T1-luc2 (Thermo Fisher Scientific, Waltham, MA, USA; Cat. No.: 21870-076) Minimum essential medium (MEM) for MDA-luc2 and 143B (Sigma-Aldrich, St. Louis, MO, USA; Cat. No.: M5650) Dulbecco’s modified eagle medium (DMEM) for NHDF (Sigma-Aldrich; Cat. No.: D5671) Fetal bovine serum (FBS) (GE Healthcare Bio-Sciences, Pittsburgh, PA, USA; Cat. No.: SH30071.03) 10X Trypsin-EDTA (Thermo Fisher Scientific; Cat. no.: 15400-054) Penicillin-streptomycin-neomycin (PSN) (Thermo Fisher Scientific; Cat. No.: 15640-055) Phosphate-buffered saline (PBS) (Sigma-Aldrich; Cat. no.: 806544) RediFect red-fluc-puromycin lentiviral particles (PerkinElmer; Waltham, MA, USA; Cat. no.: CLS960002) Puromycin (Invivogen, Pak Shek Kok, Hong Kong; Cat. No.: Ant-pr-1) Hexadimethrine bromide (polybrene) (Sigma-Aldrich; Cat. no.: TR-1003-G) D-luciferin (PerkinElmer; Cat. No.: 122796) Crystal violet solution (0.1% crystal violet in 2% ethanol, Sigma-Aldrich; Cat. No.: V5265) NuncTM EasYFlaskTM cell culture flask in 25 and 75 cm2 (Thermo Fisher Scientific; Cat. No.: 156367 and 156499) Costar® 24-well clear TC-treated multiple well plates (Corning, New York, NY, USA; Cat. No.: 3524) 6.5 mm Transwell® with 8.0 μm pore polycarbonate membrane insert (Corning; Cat. No.: 3422) Sterile cotton swabs .. Equipment CO2 incubator at 37 °C with 95% humidity and 5% CO2 (Sanyo Electric, Osaka, Japan; Cat. No.: MCO-20AIC) IVIS® Spectrum in vivo imaging system (PerkinElmer; Cat. No.: IVISSPE) Inverted Bright-field/fluorescence microscopy (Olympus Life Science, Center Valley, PE, USA; Cat. No.: IX71)

Modification:

Cell Culture:

Incubation:

Article Title: 3D Cell Culture of Human Salivary Glands Using Nature-Inspired Functional Biomaterials: The Egg Yolk Plasma and Egg White
Article Snippet: The isolation of HuSG-Fibro followed the alternative protocol in Current Protocols in Cell Biology named, “Establishment of Fibroblast Cultures” [ ]. .. Briefly, human salivary tissues were minced with scalpels and incubated with 1000 U/mL of collagenase Type 1 (LS004196, Worthington, Lakewood, NJ, USA) at 37 °C for 2 h. HuSG-Fibro cells were grown in RPMI 1640 based Complete Growth Medium (21870076, ThermoFisher Scientific, Waltham, MA, USA) including, 10% fetal bovine serum (FBS), 1% 1 M HEPES, 1% non-essential amino acids, 1% L-glutamine, 1%, penicillin/streptomycin, and 1% sodium pyruvate. ..

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fetal bovine serum fbs (Thermo Fisher)

Thermo Fisher fetal bovine serum fbs

Cell cycle arrest by serum starvation abrogates HPV infection. (A) After 24 hr incubation in serum-free <t>DMEM,</t> HaCaT cells were inoculated with HPV pseudovirion hpv 16wpA-RL, and RL activity was measured after 2 d. For serum conversion, serum-free DMEM was replaced with 10% <t>FBS/DMEM</t> before virus inoculation. The expression value is shown as % infectivity to untreated cells with hpv 16wpA-RL inoculation. Columns , mean; bars , SD. (B) Flow cytometry was performed to confirm cell cycle arrest by serum starvation. The solid line indicates the HaCaT cells incubated with serum-free DMEM for 24 h, and the gray shaded area indicates control HaCaT cells in DMEM with 10% FBS.

Fetal Bovine Serum Fbs, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fetal bovine serum fbs/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
Price from $9.99 to $1999.99

fetal bovine serum fbs - by Bioz Stars, 2021-03

99/100 stars

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Cell cycle arrest by serum starvation abrogates HPV infection. (A) After 24 hr incubation in serum-free DMEM, HaCaT cells were inoculated with HPV pseudovirion hpv 16wpA-RL, and RL activity was measured after 2 d. For serum conversion, serum-free DMEM was replaced with 10% FBS/DMEM before virus inoculation. The expression value is shown as % infectivity to untreated cells with hpv 16wpA-RL inoculation. Columns , mean; bars , SD. (B) Flow cytometry was performed to confirm cell cycle arrest by serum starvation. The solid line indicates the HaCaT cells incubated with serum-free DMEM for 24 h, and the gray shaded area indicates control HaCaT cells in DMEM with 10% FBS.

Journal: PLoS Pathogens

Article Title: Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression

doi: 10.1371/journal.ppat.1000318

Figure Lengend Snippet: Cell cycle arrest by serum starvation abrogates HPV infection. (A) After 24 hr incubation in serum-free DMEM, HaCaT cells were inoculated with HPV pseudovirion hpv 16wpA-RL, and RL activity was measured after 2 d. For serum conversion, serum-free DMEM was replaced with 10% FBS/DMEM before virus inoculation. The expression value is shown as % infectivity to untreated cells with hpv 16wpA-RL inoculation. Columns , mean; bars , SD. (B) Flow cytometry was performed to confirm cell cycle arrest by serum starvation. The solid line indicates the HaCaT cells incubated with serum-free DMEM for 24 h, and the gray shaded area indicates control HaCaT cells in DMEM with 10% FBS.

Article Snippet: Cell lines Human embryonic kidney cell line 293T from ATCC, and its enhanced SV40 T antigen-expressing daughter cell line 293TT from John Schiller, were maintained in Dulbecco's modified eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS) (Invitrogen).

Techniques: Infection, Incubation, Activity Assay, Expressing, Flow Cytometry, Cytometry

Cell cycle arrest does not inhibit influenza virus. (A) After 24 hr synchronization with aphidicolin and 4 hr treatment with etoposide or aphidicolin (3 µM each), 293T cells were inoculated in parallel with hpv 16wpA-RL or an influenza virus vector in which the hemagglutinin and neuraminidase open reading frames in viral RNA were replaced with those of vesicular stomatitis virus glycoprotein and RL, respectively [50] . (B) After 24 hr synchronization in serum-free DMEM, HaCaT cells were inoculated with hpv 16wpA-RL and the RL-expressing influenza virus as (A) in the presence or absence of FBS. RL activity was measured after 48 hrs, as described in Materials and Methods , normalized to RL activity in equivalently inoculated cells maintained in 10% FBS, and expressed in the histograms as % infectivity. Columns , mean; bars , SD.

Journal: PLoS Pathogens

Article Title: Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression

doi: 10.1371/journal.ppat.1000318

Figure Lengend Snippet: Cell cycle arrest does not inhibit influenza virus. (A) After 24 hr synchronization with aphidicolin and 4 hr treatment with etoposide or aphidicolin (3 µM each), 293T cells were inoculated in parallel with hpv 16wpA-RL or an influenza virus vector in which the hemagglutinin and neuraminidase open reading frames in viral RNA were replaced with those of vesicular stomatitis virus glycoprotein and RL, respectively [50] . (B) After 24 hr synchronization in serum-free DMEM, HaCaT cells were inoculated with hpv 16wpA-RL and the RL-expressing influenza virus as (A) in the presence or absence of FBS. RL activity was measured after 48 hrs, as described in Materials and Methods , normalized to RL activity in equivalently inoculated cells maintained in 10% FBS, and expressed in the histograms as % infectivity. Columns , mean; bars , SD.

Techniques: Plasmid Preparation, Expressing, Activity Assay, Infection

Chondrogenic differentiation of hiPSC. ( a ) Classical chondrogenic differentiation of hiPSCs via formation of embryoid bodies, outgrowth of endodermal ( green ), ectodermal ( yellow ) and mesodermal ( red ) cell lineages, selection of mesodermal cells, and induction of MSC and induction of chondrocytes. In this method hiPS cells were detached from matrigel coated dish and moved to ultra low attachment culture dish for 5 days to induce the EB formation, then EBs moved to plastic culture dish to select the hMSCs by collecting the outgrowing cells from EB (from day 5 to day 14) after collecting the attached fibroblast-like cells. These cells were cultured for 3 weeks in media containing FBS to prepare the hiPSC-MSCs (day 35 of differentiation). Then, hiPSC-MSCs were differentiated in a pellet culture system using serum free chondrogenic media for 3 weeks. ( b ) Embryoid body free method of direct differentiation of hiPSCs into hiPSC-MSCs, followed by chondrogenic differentiation. In embryoid body free method hiPSCs were cultured in matrigel coated dish and media was changed to hMSC media (DMEM supplemented with FBS) for 5 days to induce the hMSC differentiation (Day 5). Then, cells were detached and moved to a plastic culture dish for 4 passages to prepare the hiPSC-MSCs (Day 28). To differentiate the hiPSC-MSCs to chondrocytes, cells were used in pellet culture system using serum free chondrogenic media for 3 weeks

Journal: Stem Cell Reviews

Article Title: Improved Approach for Chondrogenic Differentiation of Human Induced Pluripotent Stem Cells

doi: 10.1007/s12015-014-9581-5

Figure Lengend Snippet: Chondrogenic differentiation of hiPSC. ( a ) Classical chondrogenic differentiation of hiPSCs via formation of embryoid bodies, outgrowth of endodermal ( green ), ectodermal ( yellow ) and mesodermal ( red ) cell lineages, selection of mesodermal cells, and induction of MSC and induction of chondrocytes. In this method hiPS cells were detached from matrigel coated dish and moved to ultra low attachment culture dish for 5 days to induce the EB formation, then EBs moved to plastic culture dish to select the hMSCs by collecting the outgrowing cells from EB (from day 5 to day 14) after collecting the attached fibroblast-like cells. These cells were cultured for 3 weeks in media containing FBS to prepare the hiPSC-MSCs (day 35 of differentiation). Then, hiPSC-MSCs were differentiated in a pellet culture system using serum free chondrogenic media for 3 weeks. ( b ) Embryoid body free method of direct differentiation of hiPSCs into hiPSC-MSCs, followed by chondrogenic differentiation. In embryoid body free method hiPSCs were cultured in matrigel coated dish and media was changed to hMSC media (DMEM supplemented with FBS) for 5 days to induce the hMSC differentiation (Day 5). Then, cells were detached and moved to a plastic culture dish for 4 passages to prepare the hiPSC-MSCs (Day 28). To differentiate the hiPSC-MSCs to chondrocytes, cells were used in pellet culture system using serum free chondrogenic media for 3 weeks

Article Snippet: Osteogenic differentiation was induced by culturing 6 × 104 cells/cm2 in osteogenic differentiation medium consisting of DMEM supplemented by 10 % FBS (Gibco), 100 U/ml penicillin, 100 μg/ml streptomycin (Gibco), 10 % L-Glutamine (Gibco), 50 μg/ml L-ascorbic acid 2-phosphate sequimagnesium (Sigma), 100 μg/ml MEM sodium pyruvate (Gibco), 0.1 μM dexamethasone (Sigma), and 100 mM b-glycerophosphate.

Techniques: Selection, Cell Culture

Promoter activity analysis of the bovine PDHB gene. a. We transferred six serial deletion constructs in pGL3-basic into C2C12 cells. After 5 h we replaced the transfection mixture with DMEM with 5% FBS (myoblasts) or 2% HS (myotubes). b. We transferred the same constructs into 3T3-L1 cells. We normalized relative luciferase activities to Renilla luciferase activity. The transcription factor binding sites of MYOG and C/EBPß are indicated with closed circles and ellipses, respectively. *, P

Journal: PLoS ONE

Article Title: Molecular Characterization and Transcriptional Regulation Analysis of the Bovine PDHB Gene

doi: 10.1371/journal.pone.0157445

Figure Lengend Snippet: Promoter activity analysis of the bovine PDHB gene. a. We transferred six serial deletion constructs in pGL3-basic into C2C12 cells. After 5 h we replaced the transfection mixture with DMEM with 5% FBS (myoblasts) or 2% HS (myotubes). b. We transferred the same constructs into 3T3-L1 cells. We normalized relative luciferase activities to Renilla luciferase activity. The transcription factor binding sites of MYOG and C/EBPß are indicated with closed circles and ellipses, respectively. *, P

Article Snippet: Cell culture, transfection and dual-luciferase reporter assay We cultured the mouse myoblast cell line (C2C12) and the 3T3-L1 cell line in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS) (GIBCO-Invitrogen) under humidified air containing 5% CO2 at 37°C.

Techniques: Activity Assay, Construct, Transfection, Luciferase, Binding Assay

$Binding studies of Z mab25 or protein G with fetal bovine serum and species selective affinity recovery of two monoclonal antibodies. a 10% FBS was flowed over a Z mab25 ( gray solid trace ) or protein G C2–C3 fragment (SPG) ( black dashed trace ) BIAcore biosensor surface. For comparison, a sample containing 10% FBS spiked with mouse IgG 1 mAb3 was also flowed over the Z mab25 surface ( black solid trace ). b : SDS-PAGE analysis (reducing conditions) of samples, flow-through (FT), and eluate (E) fractions from affinity chromatography experiments using either a protein G (SPG) column or a Z mab25 column, and samples of 10% FBS only ( lanes 1 – 6 ) or 10% FBS with in-spiked mouse IgG 1 mAb3 ( lanes 7 – 12 ) or 10% FBS with in-spiked mouse IgG 1 8F11 ( lanes 13 – 15 ). M LMW-SDS molecular weight marker; lane 1 : 10% FBS sample; lane 2 : SPG column, FT; lane 3 : SPG column, E; lane 4 : 10% FBS sample; lane 5 : Z mab25 column, FT; lane 6 : Z mab25 column, E; lane 7 : 10% FBS + mAb3 sample; lane 8 : SPG column, FT; lane 9 : SPG column, E; lane 10 : 10% FBS + mAb3 sample; lane 11 : Z mab25 column, FT; lane 12 : Z mab25 column, E; lane 13 : 10% FBS + mAb 8F11 sample; lane 14 : Z mab25 column, FT; lane 15 : Z mab25 column, E. The black arrows to the right indicate nominal molecular weights of antibody heavy and light chains, respectively. The numbers to the left indicate molecular weights in kilo Dalton (kDa). c Results from a biosensor analysis of pH neutralized eluates from the SPG and Z mab25 columns, originating from the use of the 10% FBS sample containing in-spiked mAb3 ( 1 – 4 ) or mAb 8F11 ( 5 , 6 ). On separate flow cell surfaces, anti-cow IgG and anti-mouse Ig antibodies were immobilized, and samples were injected. (1) black solid trace SPG column eluate, anti-cow IgG surface; (2) black dashed trace SPG column eluate, anti-mouse Ig surface; (3) gray solid trace Z mab25 column eluate, anti-cow IgG surface; (4) gray dashed trace Z mab25 column eluate, anti-mouse Ig surface; (5) black dotted trace Z mab25 column eluate, anti-cow IgG surface; (6) gray dotted trace Z mab25 column eluate, anti-mouse Ig surface$

Journal: Molecular Biotechnology

Article Title: Ribosome Display Selection of a Murine IgG1 Fab Binding Affibody Molecule Allowing Species Selective Recovery Of Monoclonal Antibodies

doi: 10.1007/s12033-010-9367-1

Figure Lengend Snippet: Binding studies of Z mab25 or protein G with fetal bovine serum and species selective affinity recovery of two monoclonal antibodies. a 10% FBS was flowed over a Z mab25 ( gray solid trace ) or protein G C2–C3 fragment (SPG) ( black dashed trace ) BIAcore biosensor surface. For comparison, a sample containing 10% FBS spiked with mouse IgG 1 mAb3 was also flowed over the Z mab25 surface ( black solid trace ). b : SDS-PAGE analysis (reducing conditions) of samples, flow-through (FT), and eluate (E) fractions from affinity chromatography experiments using either a protein G (SPG) column or a Z mab25 column, and samples of 10% FBS only ( lanes 1 – 6 ) or 10% FBS with in-spiked mouse IgG 1 mAb3 ( lanes 7 – 12 ) or 10% FBS with in-spiked mouse IgG 1 8F11 ( lanes 13 – 15 ). M LMW-SDS molecular weight marker; lane 1 : 10% FBS sample; lane 2 : SPG column, FT; lane 3 : SPG column, E; lane 4 : 10% FBS sample; lane 5 : Z mab25 column, FT; lane 6 : Z mab25 column, E; lane 7 : 10% FBS + mAb3 sample; lane 8 : SPG column, FT; lane 9 : SPG column, E; lane 10 : 10% FBS + mAb3 sample; lane 11 : Z mab25 column, FT; lane 12 : Z mab25 column, E; lane 13 : 10% FBS + mAb 8F11 sample; lane 14 : Z mab25 column, FT; lane 15 : Z mab25 column, E. The black arrows to the right indicate nominal molecular weights of antibody heavy and light chains, respectively. The numbers to the left indicate molecular weights in kilo Dalton (kDa). c Results from a biosensor analysis of pH neutralized eluates from the SPG and Z mab25 columns, originating from the use of the 10% FBS sample containing in-spiked mAb3 ( 1 – 4 ) or mAb 8F11 ( 5 , 6 ). On separate flow cell surfaces, anti-cow IgG and anti-mouse Ig antibodies were immobilized, and samples were injected. (1) black solid trace SPG column eluate, anti-cow IgG surface; (2) black dashed trace SPG column eluate, anti-mouse Ig surface; (3) gray solid trace Z mab25 column eluate, anti-cow IgG surface; (4) gray dashed trace Z mab25 column eluate, anti-mouse Ig surface; (5) black dotted trace Z mab25 column eluate, anti-cow IgG surface; (6) gray dotted trace Z mab25 column eluate, anti-mouse Ig surface

Article Snippet: For analysis of Zmab25 or protein G C2–C3 domain interaction with fetal bovine serum (FBS), a third CM5 sensor chip was prepared onto which 488 RU of protein G C2–C3 and 1817 RU of Zmab25 were immobilized on separate surfaces, and 100 μl of 10% FBS (Gibco) or 10% FBS and 133 nM mAb3 were flowed over both surfaces.

Techniques: Binding Assay, SDS Page, Flow Cytometry, Affinity Chromatography, Molecular Weight, Marker, Injection