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Corning Life Sciences non-adherent suspension culture dishes
Non Adherent Suspension Culture Dishes, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/non-adherent+suspension+culture+dishes/non+adherent+suspension+culture+dishes/pmc11475545-355-39-43
Average 90 stars, based on 1 article reviews
non-adherent suspension culture dishes - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Cell Culture:

Article Title: The comparative study revealed that the hTERT-CSF cell line was the most susceptible cell to the Lumpy skin disease virus infection among eleven cells.
Article Snippet: In brief Sun et al. establish human neurons with loss of autophagy where depletion of nicotinamide adenine dinucleotide (NAD) mediates cytotoxicity.. Boosting NAD levels improves the viability of autophagy-deficient human neurons by restoring mitochondrial bioenergetics and proteostasis, providing insights for therapeutic interventions in neurodegenerative diseases associated with autophagy dysfunction.

Article Title: Methods and compositions related to induced sensory neurons
Article Snippet: The EBs were cultured for 7 days in non-adherent suspension culture dishes (Corning), 2 days in 20% KSR medium and the following 5 days in 10% FBS DMEM.

Article Title: Autophagy promotes cell survival by maintaining NAD levels.
Article Snippet: Differentiation of hiPSCs into neural precursors and human neurons Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described.35,54 hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NPmedium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 mM SB431542 for the first 4 days.

Article Title: Isolated naive pluripotent stem cells and methods of generating same
Article Snippet: Differentiation Assays of human iPSCs and ESCs—For embryoid body (EB) induced differentiation, naive hESCs/hiPSCs were trypsinized and cultured for 6-8 days in non-adherent suspension culture dishes (Corning) in DMEM supplemented with 15% fetal bovine serum.

Article Title: NAD depletion mediates cytotoxicity in human neurons with autophagy deficiency
Article Snippet: 20 The hESC colonies were collected using 1.5 mg/mL collagenase type IV (Thermo Fisher Scientific), separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % penicillin/streptomycin, 1 % L-glutamine and 1 % non-essential amino acids (all from Gibco) supplemented with 500 ng/mL human recombinant Noggin (Peprotech) and 10 μM SB431542 (Stemgent) for the first 4 days.

Article Title: Autophagy promotes cell survival by maintaining NAD levels
Article Snippet: Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described., hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 μM SB431542 for the first 4 days.

Article Title: Diverse reprogramming codes for neuronal identity.
Article Snippet: The embryoid bodies were cultured for seven days in non-adherent suspension culture dishes (Corning), two days in mTeSR medium (StemCell Technologies) and the following five days in DMEM containing 10% FBS (vol/vol).

Suspension:

Article Title: The comparative study revealed that the hTERT-CSF cell line was the most susceptible cell to the Lumpy skin disease virus infection among eleven cells.
Article Snippet: In brief Sun et al. establish human neurons with loss of autophagy where depletion of nicotinamide adenine dinucleotide (NAD) mediates cytotoxicity.. Boosting NAD levels improves the viability of autophagy-deficient human neurons by restoring mitochondrial bioenergetics and proteostasis, providing insights for therapeutic interventions in neurodegenerative diseases associated with autophagy dysfunction.

Article Title: Methods and compositions related to induced sensory neurons
Article Snippet: The EBs were cultured for 7 days in non-adherent suspension culture dishes (Corning), 2 days in 20% KSR medium and the following 5 days in 10% FBS DMEM.

Article Title: Autophagy promotes cell survival by maintaining NAD levels.
Article Snippet: Differentiation of hiPSCs into neural precursors and human neurons Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described.35,54 hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NPmedium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 mM SB431542 for the first 4 days.

Article Title: Isolated naive pluripotent stem cells and methods of generating same
Article Snippet: Differentiation Assays of human iPSCs and ESCs—For embryoid body (EB) induced differentiation, naive hESCs/hiPSCs were trypsinized and cultured for 6-8 days in non-adherent suspension culture dishes (Corning) in DMEM supplemented with 15% fetal bovine serum.

Article Title: NAD depletion mediates cytotoxicity in human neurons with autophagy deficiency
Article Snippet: 20 The hESC colonies were collected using 1.5 mg/mL collagenase type IV (Thermo Fisher Scientific), separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % penicillin/streptomycin, 1 % L-glutamine and 1 % non-essential amino acids (all from Gibco) supplemented with 500 ng/mL human recombinant Noggin (Peprotech) and 10 μM SB431542 (Stemgent) for the first 4 days.

Article Title: Autophagy promotes cell survival by maintaining NAD levels
Article Snippet: Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described., hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 μM SB431542 for the first 4 days.

Article Title: Diverse reprogramming codes for neuronal identity.
Article Snippet: The embryoid bodies were cultured for seven days in non-adherent suspension culture dishes (Corning), two days in mTeSR medium (StemCell Technologies) and the following five days in DMEM containing 10% FBS (vol/vol).

Recombinant:

Article Title: The comparative study revealed that the hTERT-CSF cell line was the most susceptible cell to the Lumpy skin disease virus infection among eleven cells.
Article Snippet: In brief Sun et al. establish human neurons with loss of autophagy where depletion of nicotinamide adenine dinucleotide (NAD) mediates cytotoxicity.. Boosting NAD levels improves the viability of autophagy-deficient human neurons by restoring mitochondrial bioenergetics and proteostasis, providing insights for therapeutic interventions in neurodegenerative diseases associated with autophagy dysfunction.

Article Title: Methods and compositions related to induced sensory neurons
Article Snippet: The EBs were cultured for 7 days in non-adherent suspension culture dishes (Corning), 2 days in 20% KSR medium and the following 5 days in 10% FBS DMEM.

Article Title: Autophagy promotes cell survival by maintaining NAD levels.
Article Snippet: Differentiation of hiPSCs into neural precursors and human neurons Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described.35,54 hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NPmedium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 mM SB431542 for the first 4 days.

Article Title: Isolated naive pluripotent stem cells and methods of generating same
Article Snippet: Differentiation Assays of human iPSCs and ESCs—For embryoid body (EB) induced differentiation, naive hESCs/hiPSCs were trypsinized and cultured for 6-8 days in non-adherent suspension culture dishes (Corning) in DMEM supplemented with 15% fetal bovine serum.

Article Title: NAD depletion mediates cytotoxicity in human neurons with autophagy deficiency
Article Snippet: 20 The hESC colonies were collected using 1.5 mg/mL collagenase type IV (Thermo Fisher Scientific), separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % penicillin/streptomycin, 1 % L-glutamine and 1 % non-essential amino acids (all from Gibco) supplemented with 500 ng/mL human recombinant Noggin (Peprotech) and 10 μM SB431542 (Stemgent) for the first 4 days.

Article Title: Autophagy promotes cell survival by maintaining NAD levels
Article Snippet: Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described., hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 μM SB431542 for the first 4 days.

Article Title: Diverse reprogramming codes for neuronal identity.
Article Snippet: The embryoid bodies were cultured for seven days in non-adherent suspension culture dishes (Corning), two days in mTeSR medium (StemCell Technologies) and the following five days in DMEM containing 10% FBS (vol/vol).

Inhibition:

Article Title: The comparative study revealed that the hTERT-CSF cell line was the most susceptible cell to the Lumpy skin disease virus infection among eleven cells.
Article Snippet: In brief Sun et al. establish human neurons with loss of autophagy where depletion of nicotinamide adenine dinucleotide (NAD) mediates cytotoxicity.. Boosting NAD levels improves the viability of autophagy-deficient human neurons by restoring mitochondrial bioenergetics and proteostasis, providing insights for therapeutic interventions in neurodegenerative diseases associated with autophagy dysfunction.

Article Title: Methods and compositions related to induced sensory neurons
Article Snippet: The EBs were cultured for 7 days in non-adherent suspension culture dishes (Corning), 2 days in 20% KSR medium and the following 5 days in 10% FBS DMEM.

Article Title: Autophagy promotes cell survival by maintaining NAD levels.
Article Snippet: Differentiation of hiPSCs into neural precursors and human neurons Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described.35,54 hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NPmedium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 mM SB431542 for the first 4 days.

Article Title: Isolated naive pluripotent stem cells and methods of generating same
Article Snippet: Differentiation Assays of human iPSCs and ESCs—For embryoid body (EB) induced differentiation, naive hESCs/hiPSCs were trypsinized and cultured for 6-8 days in non-adherent suspension culture dishes (Corning) in DMEM supplemented with 15% fetal bovine serum.

Article Title: NAD depletion mediates cytotoxicity in human neurons with autophagy deficiency
Article Snippet: 20 The hESC colonies were collected using 1.5 mg/mL collagenase type IV (Thermo Fisher Scientific), separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % penicillin/streptomycin, 1 % L-glutamine and 1 % non-essential amino acids (all from Gibco) supplemented with 500 ng/mL human recombinant Noggin (Peprotech) and 10 μM SB431542 (Stemgent) for the first 4 days.

Article Title: Autophagy promotes cell survival by maintaining NAD levels
Article Snippet: Differentiation of hiPSCs into neural precursor cells (NPs) and terminally differentiated human neurons were performed as previously described., hiPSC colonies were collected using 1.5 mg/mL collagenase type IV, separated from the MEF feeder cells by gravity, and cultured in non-adherent suspension culture dishes (Corning) in NP medium (NPM) comprising of DMEM/F12 supplemented with 2 % B27, 1 % L-glutamine, 1 % nonessential amino acids and 1 % penicillin/streptomycin supplemented with 500 ng/mL human recombinant Noggin and 10 μM SB431542 for the first 4 days.

Article Title: Diverse reprogramming codes for neuronal identity.
Article Snippet: The embryoid bodies were cultured for seven days in non-adherent suspension culture dishes (Corning), two days in mTeSR medium (StemCell Technologies) and the following five days in DMEM containing 10% FBS (vol/vol).



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