HeLa In Vitro Colony Formation Assay (Cell Proliferation)
CAT#: ITS-1022-YF5169
Target Cell Organism: Human
Target Cell Name: HeLa
Assay Type: Cell Viability/Cytotoxicity and Antiproliferative Assays
Assay Overview
This assay is to provide HeLa-based In Vitro Colony Formation Assay (Cell Proliferation) to accelerate our client's oncology projects. The assay will be customized according to the specific requirements. Please contact our scientists to discuss more details.
Target Cell Name
HeLa
Target Cell Organism
Human
Target Cell Background
In 1952, HeLa cells became the first human cell line that could grow and divide endlessly in a laboratory, leading scientists to label these cells "immortal". The immortality of HeLa cells contributed to their adoption across the world as the human cell line of choice for biomedical research.
Related Diseases
Cervical Cancer
Research Area
Oncology
Assay Name
In Vitro Colony Formation Assay (Cell Proliferation)
Short Description
HeLa-cell based In Vitro Colony Formation Assay (Cell Proliferation)
Assay Description
Colony formation assay is one of the widely used assays based on the ability of cancer cells to form into colonies. This assay is useful to determine the effects of a drug or external stimuli such as radiation on clonogenic growth of cancer cells. This can be easily carried out for any type of cancer cells grown as a monolayer or as non-adherent cells. Before starting cell seeding, all the cells to be plated must be properly detached to avoid colonies at the starting point. A colony must contain a minimum of 50 cells and formed colonies are counted after staining with a suitable dye such as trypan blue. A microscope is usually used to visualize cell colonies and counting is normally carried out manually.
Assay Type
Cell Viability/Cytotoxicity and Antiproliferative Assays
Assay Type Details
Uncontrolled proliferation is one of the main features of cancer cells. Cell-based in vitro assays are employed to determine whether test molecules possess direct cytotoxic/antiproliferative effects in cancer cells.