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AB235694

Cell Migration/Chemotaxis Assay Kit (24-well, 8 µm)

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(3 Publications)

Cell Migration/Chemotaxis Assay Kit (24-well, 8 µm) (ab235694) is a trans-well migration assay using a Boyden chamber, where cells migrate through a semi-permeable membrane under different stimuli.

- Ready-to-use buffers, dissociation solution, migration inducer, and cell dye
- Includes Boyden cell migration chamber
2 Images
Functional Studies - Cell Migration/Chemotaxis Assay Kit (24-well, 8 µm) (AB235694)
  • FuncS

Supplier Data

Functional Studies - Cell Migration/Chemotaxis Assay Kit (24-well, 8 µm) (AB235694)

Standard Curve.

HT-1080 cells were harvested, counted and serially diluted to obtain desired cell number. Cells were incubated according to the protocol.

Functional Studies - Cell Migration/Chemotaxis Assay Kit (24-well, 8 µm) (AB235694)
  • FuncS

Supplier Data

Functional Studies - Cell Migration/Chemotaxis Assay Kit (24-well, 8 µm) (AB235694)

Cell Invasion

Key facts

Detection method

Fluorescent

Sample types

Suspension cells, Adherent cells

Assay Platform

Microplate reader

Product details

Cell Migration/Chemotaxis Assay Kit (24-well, 8 μm) (ab235694) utilizes a Boyden chamber, where the cells migrate through a semi-permeable membrane under different stimuli. Cell migration can be analyzed directly by reading fluorescence (Ex/Em = 530/590 nm) in a plate reader. Our assay is easy to use, sensitive and adaptable to high-throughput systems.

Cell migration / chemotaxis assay protocol summary
- Grow cells.
- Add cell culture media containing desired chemoattractant to the bottom part of the Boyden chamber (bottom chamber).
- Add cell culture media containing positive control Migration Inducer to control wells in the bottom chamber.
- Add cells to the top part of the Boyden chamber (top chamber) with any desired treatment.
- Incubate at 37°C in cell culture incubator for 2-48 h.
- Cells will migrate through the polycarbonate membrane from the top chamber to the bottom chamber.
- Remove the top chamber and remove media and remaining cells.
- Centrifuge the bottom chamber and wash cells with Wash Buffer, repeat.
- Add Cell Dye / Cell Disassociation Solution to bottom chamber and incubate for 60-min in cell culture incubator.
- Transfer to 96-well plate and analyze with fluorometric (Ex/Em 530/590 nm) plate reader.
- Prepare a separate standard curve with known numbers of cells in a 96-well plate with Cell Dye, incubate for 1-hr, and analyze with fluorometric (Ex/Em 530/590 nm) plate reader to allow quantitation.

Other notes
This product was previously called K909 Biovision EZCell™ Cell Migration/Chemotaxis Assay Kit (24-well, 8 μm). Biovision was acquired by Abcam in 2021.

Cell invasion is the ability of cells to migrate from one area to another through an extracellular matrix. Cell invasion is exhibited by both normal cells as well as cancerous cells in response to specific external signals, including chemical and mechanical stimuli. During invasion, extracellular matrix is enzymatically degraded by cellular proteases before cells migrate to the new location. Cell invasion is required for normal processes such as wound repair, vasculature formation and the inflammatory response as well as the abnormal invasion of tissues by tumor cells during metastasis.

The Safety Datasheet for this product has been updated for certain countries. Please check the current version in the Support and downloads section.

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
-20°C

Product protocols

Target data

Publications (3)

Recent publications for all applications. Explore the full list and refine your search

American journal of human genetics 111:2232-2252 PubMed39226899

2024

ARID1A-BAF coordinates ZIC2 genomic occupancy for epithelial-to-mesenchymal transition in cranial neural crest specification.

Applications

Unspecified application

Species

Unspecified reactive species

Samantha M Barnada,Aida Giner de Gracia,Cruz Morenilla-Palao,Maria Teresa López-Cascales,Chiara Scopa,Francis J Waltrich,Harald M M Mikkers,Maria Elena Cicardi,Jonathan Karlin,Davide Trotti,Kevin A Peterson,Samantha A Brugmann,Gijs W E Santen,Steven B McMahon,Eloísa Herrera,Marco Trizzino

Biomedicines 10: PubMed35327461

2022

Extracellular Vesicles Derived from Acidified Metastatic Melanoma Cells Stimulate Growth, Migration, and Stemness of Normal Keratinocytes.

Applications

Unspecified application

Species

Unspecified reactive species

Maxim L Bychkov,Artem V Kirichenko,Irina N Mikhaylova,Alexander S Paramonov,Evgeny V Yastremsky,Mikhail P Kirpichnikov,Mikhail A Shulepko,Ekaterina N Lyukmanova

Biomedicines 9: PubMed34680442

2021

Mambalgin-2 Inhibits Growth, Migration, and Invasion of Metastatic Melanoma Cells by Targeting the Channels Containing an ASIC1a Subunit Whose Up-Regulation Correlates with Poor Survival Prognosis.

Applications

Unspecified application

Species

Unspecified reactive species

Maxim L Bychkov,Artem V Kirichenko,Mikhail A Shulepko,Irina N Mikhaylova,Mikhail P Kirpichnikov,Ekaterina N Lyukmanova
View all publications
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