Spectral chromosome karyotyping experiments
Throughout the history of clinical cytogenetics, G-banding has served as the "gold standard" for detecting total chromosomal abnormalities in clinical samples,
Knowledge Base
Laboratory Protocols & SOPs Library
3,200+ step-by-step lab protocols and SOPs for cell culture, staining, PCR, protein work and microbiology, with reagents, conditions and evaluation criteria.
3228 articles
Liposomal vectors for direct in vivo gene transfection experiments
Many of the cationic liposomes used for liposomal transfection of cells in tissue cultures are able to be purchased. Composition optimization is highly dependen
Diagnosis of Fanconi anemia (congenital myelodysplasia)--dioxobutane (dibutyl epoxide) detection assay
Fanconi anemia (FA) is an autosomal recessive syndrome characterized by progressive bone marrow failure and an increased risk of malignancies, particularly acut
Meiosis mapping experiment
Currently, genetic mapping techniques can be used as a way to monitor the means of genomic manipulation, which needs to be realized through the use of molecular
Nuclease digestion of purified genomic DNA by Micrococcus spp.
MNase can cut DNA non-randomly. therefore, to determine how this naturally non-random pattern is affected by nuclear proteins such as histones, it is important
Experiments to identify chromatin-bound proteins from total cell extracts by immunoprecipitation methods
This experiment is both a simple and very sensitive method for determining whether a known protein in Saccharomyces cerevisiae binds to a known DNA sequence. So
Experiments on the effect of environment on gene expression in Drosophila
Many aspects of phenotype are influenced by the genetic composition of an organism and the environment in which it lives, so it can be said that phenotype is a
Experimental application of fluorescence in situ hybridization in the preimplantation diagnosis of aneuploidy
Pre-implantation Genetic Diagnosis (PGD), as a major new method of preventing genetic disorders, avoids the need for prenatal diagnosis and the possibility of t
Fluorescent genotyping screening for tiny subtelomeric rearrangement assay
Our results strongly support the notion that microtelomeric rearrangements play a very important role in spontaneous mental retardation (approximately 12% in ou