T25 Flask Culture

T25 flask culture is a laboratory method for growing adherent cells in a sterile tissue-culture flask with a 25 cm² growth surface, providing a controlled environment for maintaining and studying cell populations. Cells are seeded in nutrient medium, attach to the treated plastic surface, and proliferate under regulated temperature, carbon dioxide, humidity, and aseptic conditions; the medium is periodically replaced to support viability. Researchers use T25 cultures to expand cells, assess morphology and growth, and prepare material for downstream experiments such as drug-response or molecular analyses. Because the format supports consistent handling at modest scale, it is widely used in teaching laboratories and routine biological research.

T25 Flask Culture - Related Videos

Research

JoVE Journal - Biology
Free Sample

Scale-Up of Mammalian Cell Culture using a New Multilayered Flask

0 Views •

Cited by 4 •

2011

Cells play an instrumental and increasing role in research, and the discovery and development of new therapeutics. With this increasing need for greater number of cells we need more efficient and effective ways for growing and harvesting attachment dependent cells. A Multilayered flask with the right features can serve this purpose.

Research

JoVE EoE - Neuronal Culture Techniques

Isolation and Culture of Primary Schwann Cells from a Human Dermis

0 Views •

2025

This video demonstrates a protocol for isolating and culturing Schwann cells from human dermis tissues. The human dermis contains various cell types, including fibroblasts and Schwann cells. After isolation, the cells are treated with an antimitotic agent to eliminate proliferating fibroblasts, resulting in a pure culture of Schwann cells.

Transient Expression and Cellular Localization of Recombinant Proteins in Cultured Insect Cells

0 Views •

Cited by 6 •

2017

Nonlytic insect cell expression systems are underutilized for production, cellular trafficking/localization, and recombinant protein functional analysis. Here, we describe methods to generate expression vectors and subsequent transient protein expression in commercially available lepidopteran cell lines. The co-localization of Bemisia tabaci aquaporins with subcellular fluorescent marker proteins is also presented.

Splitting Spheroids for Sub-culturing and Shipping: A Procedure for Propagating and Transferring Spheroids from Small Bowel Neuroendocrine Tumor

0 Views •

2023

This video demonstrates a strategy to split and propagate spheroids developed from small bowel neuroendocrine tumor cells. These spheroids have small bowel neuroendocrine tumor markers and can be propagated and further used to test anti-cancer drugs.

Obtaining a Mixed Oligodendrocyte and Astrocyte Culture From Adult Mouse Neural Stem Cells

0 Views •

2025

This video demonstrates a detailed protocol for isolating the lateral ventricle walls from the adult mouse brain and performing enzymatic tissue dissociation to obtain single cells. These cells are then subjected to specific culture conditions that selectively enhance the proliferation of neural stem cells and promote their differentiation into co-cultures of oligodendrocytes and astrocytes.

View All Results

FAQs

Related Topics