LL/2 In Vitro Restriction Landmark Genome Scanning (RLGS) Assay
CAT#: ITS-1022-YF818
Target Cell Organism: Mouse
Target Cell Alternative Name: LLC1
Target Cell Name: LL/2
Assay Type: Genome Alteration Assays
Assay Overview
This assay is to provide LL/2-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
LL/2
Target Cell Organism
Mouse
Target Cell Background
LL/2 (LLC1) is a cell line established from the lung of a C57BL mouse bearing a tumor resulting from an implantation of primary Lewis lung carcinoma.
Target Cell Alternative Name
LLC1
Related Diseases
Lewis Lung Carcinoma
Research Area
Oncology
Assay Name
In Vitro Restriction Landmark Genome Scanning (RLGS) Assay
Short Description
LL/2-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.