Karyotype analysis can be used to easily determine sex and a number of genetic disorders, such as Down's Syndrome (trisomy-21) or Klinefelter's Syndrome (XXY).
AnswerVolumetric analysis or titration is a common laboratory method of chemical analysis which can be used to determine the concentration of a known reactant; volumetry is a quantitative method of analysis.Qualitative analysis is used to separate and detect elements, functional groups, molecules etc. in a sample substance, without specifying concentration.
a karyotype
Yes a karyotype is performed which is a blood test to be able to look at the number of chromosomes a person has, and therefore would be able to identify the extra X chromosome in case someone has it.
saddly and tragically :( no im terribly sorry
The answer is,homologous chromosomes :) LOL hope that helped, even though i know it did ;)
A karyotype can detect Turner syndrome by revealing a single X chromosome in females (45,X). This genetic condition is characterized by the absence of one X chromosome, which is visible on a karyotype analysis.
karyotype analysis
An ordered display of an individual's chromosomes is called a karyotype. It is used to analyze the number, size, and shape of chromosomes to detect genetic abnormalities or chromosomal disorders.
Karyotype. A karyotype is a visual representation of an individual's chromosomes arranged by size, shape, and banding pattern. It can be used to detect genetic abnormalities, such as extra or missing chromosomes.
A karyotype can provide information about the number, size, and shape of an individual's chromosomes. This can help detect chromosomal abnormalities such as Down syndrome or Turner syndrome in a fetus.
Cells are obtained for creating a karyotype through a process called a karyotype analysis, where cells are collected from a sample of blood, bone marrow, or other tissues. These cells are then cultured and treated to stop their growth at a specific stage of cell division, allowing for the chromosomes to be stained and visualized under a microscope for analysis.
A picture that shows chromosomes arranged in pairs is called a karyotype. It is a visual representation of an individual's chromosomes organized by size, shape, and banding pattern, typically used in genetic analysis to identify chromosomal abnormalities or genetic disorders.
-Determine the gender of the individual. -To tell if 2 cells belong to the same species. -To detect the genetic abnormalities in Prenatal diagnosis.
Metallurgical analysis is the examination of metal, usually to detect cracks and weaknesses.
This is known as a karyogram.
A picture of chromosomes is called a "karyotype."
Karyotype: This is a method to detect defects in the chromosome. You make an image of the chromosomes and then order them according to number ( in human 23 pairs) and you match the 2 chromosomes of a pair. Now gross changes such as extra numbers of a pair or missing numbers. Using a method called FISH you can also give each individual chromosome a color. In this way you can detect translocations, meaning that a part of the chromosome has attached itself to another chromosome. Small changes such as deletions of a nucleotide are not detectable, for that you need to do a DNA analysis. It is used in medecine to detect the cause of certain syndromes and diseases mostly inborn, or to detect the changes in cancer cells that underlie the disease