Knockout Serum Replacement

Knockout Serum Replacement is a defined cell-culture supplement designed to replace animal serum in media used to maintain and differentiate pluripotent or progenitor cells. Its controlled mixture of nutrients, proteins, lipids, and signaling-support components promotes cell survival and growth while reducing the variability associated with undefined serum factors. In neuroscience, researchers use Knockout Serum Replacement to culture neural stem or progenitor cells and regulate their progression toward neuronal and glial lineages. This improved control supports studies of neural development, cell fate decisions, disease modeling, and experimental protocols that require more consistent and reproducible culture conditions.

Knockout Serum Replacement - Related Videos

Research

JoVE Journal - Biology
Free Sample

Cryopreserving and Recovering of Human iPS Cells using Complete KnockOut Serum Replacement Feeder-Free Medium

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Cited by 12 •

2010

This protocol describes the detailed procedure for cryopreserving human iPS cells in KnockOut SR cryopreservation medium and recovering these cells in complete KnockOut SR Feeder Free (KSR-FF) medium or feeder-based KnockOut SR medium.

Research

JoVE Journal - Biology
Free Sample

Feeder-Free Adaptation, Culture and Passaging of Human IPS Cells using Complete KnockOut Serum Replacement Feeder-Free Medium

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Cited by 14 •

2010

The following protocol provides instruction for adapting human induced Pluripotent Stem (iPS) Cells to feeder-free culture using complete KnockOut Serum Replacement Feeder-Free medium (KSR-FF). Once adapted, instructions for continual maintenance are also provided.

A Protocol for Multiple Gene Knockout in Mouse Small Intestinal Organoids Using a CRISPR-concatemer

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Cited by 17 •

2017

This protocol describes the steps for cloning multiple single guide RNAs into one guide RNA concatemer vector, which is of particular use in creating multi-gene knockouts using CRISPR/Cas9 technology. The generation of double knockouts in intestinal organoids is shown as a possible application of this method.

Research

JoVE EoE - Genome Editing Techniques

CRISPR Concatemer-Mediated Multiple Gene Knockout: A Technique to Simultaneously Knockout Multiple Genes by Non-Homologous End-Joining Pathway in Mouse Intestinal Cells

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2025

This video describes a gene knockout technique using a CRISPR-concatemer to simultaneously knock out multiple genes in cultured mouse intestinal organoid cells. This method is used to knock out a diseased gene and to elucidate the function of a gene and its paralogues.

Epigenome-Wide CRISPR-Cas9-Based Knockout Screens on Chemoresistant Cells

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2026

Here, we present a protocol for generating chemoresistant cells using a dose-escalation approach, followed by a CRISPR/Cas9-based screen using a focused sgRNA library targeting epigenetic modifiers to identify regulators of acquired chemoresistance. The protocol also provides multiple optimization points tailored to chemoresistant cell models, offering a robust framework for researchers investigating resistance mechanisms.

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