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dmem f12 with hepes  (Thermo Fisher)


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    Structured Review

    Thermo Fisher dmem f12 with hepes
    Dmem F12 With Hepes, 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/product/dmem+f12+with+hepes/HEPES/pm41922773-458-14-17
    Average 99 stars, based on 1 article reviews
    dmem f12 with hepes - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Suspension:

    Article Title: Mapping human microglial morphological diversity via handcrafted and deep learning-derived image features
    Article Snippet: Cells harvested from the supernatant were centrifuged (400g, 5 min), filtered through a 40 μm cell strainer and counted using the Countess Automated Cell Counter (Invitrogen) with Trypan Blue exclusion. .. A suspension of 160,000 cells/mL was prepared, and 50 μL (8,000 cells) was seeded per well in DMEM-F12 with HEPES (ThermoFisher), supplemented with GlutaMAX (1X), N2 supplement (1X), and freshly added recombinant human IL-34 (100 ng/mL). .. Cells were primed with 1 μg/mL LPS (Invitrogen) in IL-34 free medium.

    Recombinant:

    Article Title: Mapping human microglial morphological diversity via handcrafted and deep learning-derived image features
    Article Snippet: Cells harvested from the supernatant were centrifuged (400g, 5 min), filtered through a 40 μm cell strainer and counted using the Countess Automated Cell Counter (Invitrogen) with Trypan Blue exclusion. .. A suspension of 160,000 cells/mL was prepared, and 50 μL (8,000 cells) was seeded per well in DMEM-F12 with HEPES (ThermoFisher), supplemented with GlutaMAX (1X), N2 supplement (1X), and freshly added recombinant human IL-34 (100 ng/mL). .. Cells were primed with 1 μg/mL LPS (Invitrogen) in IL-34 free medium.

    Concentration Assay:

    Article Title: DNA damage burden causes selective CUX2 neuron loss in neuroinflammation.
    Article Snippet: .. The cell suspensions were brought to a final Percoll concentration of 22.5% by adding DMEM/F12 with HEPES (Thermo Fisher Scientific, 11-039-021) and centrifuged for 20 min at 800g. .. The supernatant was removed, and the brain cell pellet (bottom 3 ml) was resuspended in HBSS without calcium and magnesium (Thermo Fisher Scientific, 14170112), then centrifuged for a further 5 min at 300g; the supernatant was next removed and the cells were resuspended in 1 ml of red blood cell lysing buffer (SigmaAldrich, R7757).

    Generated:

    Article Title: Inflammatory reprogramming of human brain endothelial cells compromises blood–brain barrier integrity in Alzheimer’s disease
    Article Snippet: Human iPSC lines used in this study include AG09173 ( APOE3/3 parental from a healthy 75-year-old female donor) and AG09173-1336 (isogenic APOE4/4 gene-edited); AG10788 ( APOE4/4 parental from a confirmed Alzheimer’s 87-year-old female donor) and AG10788-1207 (isogenic APOE3/3 gene-edited); and ZO-1 -mEGFP iPSC line from a healthy 30-year-old male donor (Allen Institute for Cell Science; parental line WTC-11, Coriell GM25256). .. APOE3 and APOE4 cell lines were previously generated by the Picower Institute for Learning and Memory iPSC Facility, with CRISPR/Cas9 genome editing performed as previously described. iPSCs were cultured on hESC-qualified Matrigel-coated plates (Corning 354277), prepared using 2% v/v Matrigel in DMEM/F12 with HEPES (Gibco) and incubated for 30 min at 37°C. iPSCs were maintained in mTeSR1 medium and passaged using ReLeSR prior to reaching ∼60% confluence (reagents from STEMCELL Technologies). ..

    CRISPR:

    Article Title: Inflammatory reprogramming of human brain endothelial cells compromises blood–brain barrier integrity in Alzheimer’s disease
    Article Snippet: Human iPSC lines used in this study include AG09173 ( APOE3/3 parental from a healthy 75-year-old female donor) and AG09173-1336 (isogenic APOE4/4 gene-edited); AG10788 ( APOE4/4 parental from a confirmed Alzheimer’s 87-year-old female donor) and AG10788-1207 (isogenic APOE3/3 gene-edited); and ZO-1 -mEGFP iPSC line from a healthy 30-year-old male donor (Allen Institute for Cell Science; parental line WTC-11, Coriell GM25256). .. APOE3 and APOE4 cell lines were previously generated by the Picower Institute for Learning and Memory iPSC Facility, with CRISPR/Cas9 genome editing performed as previously described. iPSCs were cultured on hESC-qualified Matrigel-coated plates (Corning 354277), prepared using 2% v/v Matrigel in DMEM/F12 with HEPES (Gibco) and incubated for 30 min at 37°C. iPSCs were maintained in mTeSR1 medium and passaged using ReLeSR prior to reaching ∼60% confluence (reagents from STEMCELL Technologies). ..

    Cell Culture:

    Article Title: Inflammatory reprogramming of human brain endothelial cells compromises blood–brain barrier integrity in Alzheimer’s disease
    Article Snippet: Human iPSC lines used in this study include AG09173 ( APOE3/3 parental from a healthy 75-year-old female donor) and AG09173-1336 (isogenic APOE4/4 gene-edited); AG10788 ( APOE4/4 parental from a confirmed Alzheimer’s 87-year-old female donor) and AG10788-1207 (isogenic APOE3/3 gene-edited); and ZO-1 -mEGFP iPSC line from a healthy 30-year-old male donor (Allen Institute for Cell Science; parental line WTC-11, Coriell GM25256). .. APOE3 and APOE4 cell lines were previously generated by the Picower Institute for Learning and Memory iPSC Facility, with CRISPR/Cas9 genome editing performed as previously described. iPSCs were cultured on hESC-qualified Matrigel-coated plates (Corning 354277), prepared using 2% v/v Matrigel in DMEM/F12 with HEPES (Gibco) and incubated for 30 min at 37°C. iPSCs were maintained in mTeSR1 medium and passaged using ReLeSR prior to reaching ∼60% confluence (reagents from STEMCELL Technologies). ..

    Incubation:

    Article Title: Inflammatory reprogramming of human brain endothelial cells compromises blood–brain barrier integrity in Alzheimer’s disease
    Article Snippet: Human iPSC lines used in this study include AG09173 ( APOE3/3 parental from a healthy 75-year-old female donor) and AG09173-1336 (isogenic APOE4/4 gene-edited); AG10788 ( APOE4/4 parental from a confirmed Alzheimer’s 87-year-old female donor) and AG10788-1207 (isogenic APOE3/3 gene-edited); and ZO-1 -mEGFP iPSC line from a healthy 30-year-old male donor (Allen Institute for Cell Science; parental line WTC-11, Coriell GM25256). .. APOE3 and APOE4 cell lines were previously generated by the Picower Institute for Learning and Memory iPSC Facility, with CRISPR/Cas9 genome editing performed as previously described. iPSCs were cultured on hESC-qualified Matrigel-coated plates (Corning 354277), prepared using 2% v/v Matrigel in DMEM/F12 with HEPES (Gibco) and incubated for 30 min at 37°C. iPSCs were maintained in mTeSR1 medium and passaged using ReLeSR prior to reaching ∼60% confluence (reagents from STEMCELL Technologies). ..

    Article Title: VHL Gene Restoration Supports RCC Reprogramming to iPSCs but Does Not Ensure Line Stability
    Article Snippet: .. The cells and vector mixture were then electroporated and plated onto a 10 cm geltrex coated plate with Irvine DMEM/10% FBS media and incubated for 24 h. Day 1 post transfection the cells were switched to the N2B27 media which contained DMEM/F12 with HEPES (Invitrogen, cat# 11330-032) and 100× N2 supplement (Invitrogen, cat# 17502-048), 50× B27 supplement (Invitrogen, cat#, 17504-044), 10 mM MEM NEAA (Invitrogen, cat# 35050-061), 100× Glutamax (Invitrogen, cat# 35050-061) and 55 mM B-mercaptoethoanol (Invitrogen, cat# 21985-023). .. The N2B27 media was prepared without bFGF (Invitrogen cat# 50037-M07E) and then supplement with fresh bFGF to a final concentration of 100 ng/mL at the time of use.

    Purification:

    Article Title: Multi-site DMS probing reveals higher-order structure of RNA-protein complexes in living cells
    Article Snippet: .. Samples were then quenched with 10 volumes of 2-mercaptoethanol on ice and purified by ethanol precipitation. hTERT-RPE1 cells were maintained in DMEM-F12 with HEPES (Gibco) with 10% FBS (Gibco), 100 U/mL Pen/Strep (Gibco), 2 mM sodium pyruvate (Gibco), and MEM non-essential amino acids (Gibco) at 37 °C and 5% CO 2 . .. HeLa and HEK293T cells were maintained in DMEM with 10% FBS, 100 U/mL Pen/Strep (Gibco), 2 mM sodium pyruvate (Gibco), and MEM non-essential amino acids (Gibco) at 37 °C and 5% CO 2 .

    Ethanol Precipitation:

    Article Title: Multi-site DMS probing reveals higher-order structure of RNA-protein complexes in living cells
    Article Snippet: .. Samples were then quenched with 10 volumes of 2-mercaptoethanol on ice and purified by ethanol precipitation. hTERT-RPE1 cells were maintained in DMEM-F12 with HEPES (Gibco) with 10% FBS (Gibco), 100 U/mL Pen/Strep (Gibco), 2 mM sodium pyruvate (Gibco), and MEM non-essential amino acids (Gibco) at 37 °C and 5% CO 2 . .. HeLa and HEK293T cells were maintained in DMEM with 10% FBS, 100 U/mL Pen/Strep (Gibco), 2 mM sodium pyruvate (Gibco), and MEM non-essential amino acids (Gibco) at 37 °C and 5% CO 2 .

    Plasmid Preparation:

    Article Title: VHL Gene Restoration Supports RCC Reprogramming to iPSCs but Does Not Ensure Line Stability
    Article Snippet: .. The cells and vector mixture were then electroporated and plated onto a 10 cm geltrex coated plate with Irvine DMEM/10% FBS media and incubated for 24 h. Day 1 post transfection the cells were switched to the N2B27 media which contained DMEM/F12 with HEPES (Invitrogen, cat# 11330-032) and 100× N2 supplement (Invitrogen, cat# 17502-048), 50× B27 supplement (Invitrogen, cat#, 17504-044), 10 mM MEM NEAA (Invitrogen, cat# 35050-061), 100× Glutamax (Invitrogen, cat# 35050-061) and 55 mM B-mercaptoethoanol (Invitrogen, cat# 21985-023). .. The N2B27 media was prepared without bFGF (Invitrogen cat# 50037-M07E) and then supplement with fresh bFGF to a final concentration of 100 ng/mL at the time of use.

    Transfection:

    Article Title: VHL Gene Restoration Supports RCC Reprogramming to iPSCs but Does Not Ensure Line Stability
    Article Snippet: .. The cells and vector mixture were then electroporated and plated onto a 10 cm geltrex coated plate with Irvine DMEM/10% FBS media and incubated for 24 h. Day 1 post transfection the cells were switched to the N2B27 media which contained DMEM/F12 with HEPES (Invitrogen, cat# 11330-032) and 100× N2 supplement (Invitrogen, cat# 17502-048), 50× B27 supplement (Invitrogen, cat#, 17504-044), 10 mM MEM NEAA (Invitrogen, cat# 35050-061), 100× Glutamax (Invitrogen, cat# 35050-061) and 55 mM B-mercaptoethoanol (Invitrogen, cat# 21985-023). .. The N2B27 media was prepared without bFGF (Invitrogen cat# 50037-M07E) and then supplement with fresh bFGF to a final concentration of 100 ng/mL at the time of use.



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