Cell Removal Efficiency

Cell removal efficiency is a measure of how completely cellular material has been eliminated from a biological tissue or scaffold, an important parameter in bioengineering and decellularization. It is assessed after physical, chemical, or enzymatic treatments disrupt cell membranes, lyse cells, and remove cellular debris through rinsing or processing, while aiming to preserve the extracellular matrix. High efficiency can reduce unwanted cellular components that may trigger immune responses and improve the suitability of biomaterials for tissue engineering, regenerative medicine, and engineered grafts. Evaluating this outcome alongside matrix preservation helps researchers optimize protocols and balance biological compatibility with structural function.

Cell Removal Efficiency - Related Videos

Research

JoVE Journal - Biology

Procedure to Evaluate the Efficiency of Flocculants for the Removal of Dispersed Particles from Plant Extracts

0 Views •

Cited by 6 •

2016

The design-of-experiments procedure presented here allows the evaluation of different flocculants in terms of their ability to aggregate dispersed particles in plant extracts, thus reducing turbidity and the costs of downstream processing.

An Efficient Method to Obtain Dedifferentiated Fat Cells

0 Views •

Cited by 4 •

2016

We have modified the conditions for DFAT cell generation and provide herein information regarding the use of an improved growth medium for the production of these cells.

Rapid Fibroblast Removal from High Density Human Embryonic Stem Cell Cultures

0 Views •

Cited by 3 •

2012

Despite ongoing efforts to transition cultures to feeder-free conditions, the derivation and culture of human embryonic stem cells (hESC) remain largely dependent on co-cultures with mouse embryonic feeders (MEFs). Here, we show a novel methodology for rapidly removing feeders from hESC cultures prior to experimentation.

Efficient Differentiation of Human Pluripotent Stem Cells into Liver Cells

0 Views •

Cited by 6 •

2019

This protocol details a monolayer, serum-free method to efficiently generate hepatocyte-like cells from human pluripotent stem cells (hPSCs) in 18 days. This entails six steps as hPSCs sequentially differentiate into intermediate cell-types such as the primitive streak, definitive endoderm, posterior foregut and liver bud progenitors before forming hepatocyte-like cells.

Efficient Generation Human Induced Pluripotent Stem Cells from Human Somatic Cells with Sendai-virus

0 Views •

Cited by 13 •

2014

Here, we present our established method to reprogram human somatic cells into transgene-free human iPSCs with Sendai virus, which shows consistent outcome and enhanced efficiency.

View All Results

FAQs

Related Topics