Kasumi-3 In Vitro Restriction Landmark Genome Scanning (RLGS) Assay

CAT#: ITS-1122-YF4073
Target Cell Organism: Human
Target Cell Name: Kasumi-3
Assay Type: Genome Alteration Assays
Assay Overview
This assay is to provide Kasumi-3-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
Kasumi-3
Target Cell Organism
Human
Target Cell Background
The cell line was established from the blast cells of a myeloperoxidase-negative acute leukemia patient.
Treatment with either interleukin (IL)-2, IL-3, IL-4, granulocyte-macrophage colony-stimulating factor (GMCSF) or stem cell factor induced the proliferation, characteristic of undifferentiated leukemia.
Related Diseases
Acute Myeloblastic Leukemia; AML
Research Area
Oncology
Assay Name
In Vitro Restriction Landmark Genome Scanning (RLGS) Assay
Short Description
Kasumi-3-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
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