Chromosome gene localization experiments
Chromosomes are entities containing genes, which are only visible under the microscope as a general structure. Genes are nucleotide sequences at the molecular l
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
Experiments in the culture and preparation of samples of pregnancy products and other solid tissue sources for chromosome analysis
In clinical practice, chromosomal studies require the use of solid tissues other than tumor tissue for one of two reasons: some patients can only obtain solid t
Chromosome specimen preparation experiments for in vitro cultured cells
The source of this experiment is the official website of the Fourth Military Medical University
Experiments on the preparation of chromosome smears in the mid-division of chorionic specimens
The interstitial center of the villi includes a range of cellular components-fibroblasts, endothelial cells, and macrophages-as well as a large amount of interc
Typing experiments with autofluorescence
The typing methods described in this unit are needed when there are a large number of samples with multiple microsatellite markers to be typed. For example, a d
High-throughput genotyping experiments using the TAQMAN assay
This unit describes the application of 5'-nuclease allele specific analysis or TaqMan method for single nucleotide polymorphism (SNP) typing.
Micronucleus Detection Experiment
The MicronucleusTest was developed in the early 1970s as a rapid and simple method of detecting environmental carcinogens. Micronuclei are the remnants of chrom
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
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,