Colo205 In Vitro Restriction Landmark Genome Scanning (RLGS) Assay

CAT#: ITS-1022-YF608
Target Cell Organism: Human
Target Cell Alternative Name: COLO 205
Target Cell Name: Colo205
Assay Type: Genome Alteration Assays
Assay Overview
This assay is to provide Colo205-based In Vitro Restriction Landmark Genome Scanning (RLGS) Assay 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
Colo205
Target Cell Organism
Human
Target Cell Background
The COLO 205 cell line is made up of epithelial cells isolated in 1975 from ascitic fluid derived from a White, 70-year-old, man with colon cancer. The cells can be used for cancer and toxicology research.
Target Cell Alternative Name
COLO 205
Related Diseases
Colon Cancer
Research Area
Oncology
Assay Name
In Vitro Restriction Landmark Genome Scanning (RLGS) Assay
Short Description
Colo205-cell based In Vitro Restriction Landmark Genome Scanning (RLGS) Assay
Assay Description
Restriction landmark genome scanning is a technique used to detect genome copy number differences, mutations and gene polymorphisms. In this technique, genome is first digested with a series of restriction enzymes and the resulting fragments are labeled using radioactive isotopes. After labeling, DNA is again digested with another set of restriction enzymes and allowed to separate electrophoretically. Finally, labeled DNA fragments are then detected using autoradiography.
Assay Type
Genome Alteration Assays
Assay Type Details
Aberrant or somatic mutations are more commonly found in the DNA of cancer cells compared to normal cells. There is an equilibrium that exists between DNA damage and repair in normal cells. However, in cancer cells these events are disturbed, resulting in mutations and genomic instability. Genomic instability in cancer cells causes chromosomal aberrations, microsatellite instability, aneuploidy and uncontrolled gene amplifications and genetic instability in cancer cells are mainly due to point mutations or chromosomal aberrations such as insertions, deletions and translocation, resulting in mutated proteins.
For Research Use Only | Not For Clinical Use
Online Inquiry