0
What else can I help you with?
What is the difference between volumetric analysis and gravimetric analysis?
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 photograph of human chromosomes that may be studied to determine possible genetic disorders is known as?
a karyotype
Is there a genetic test for klinefelter's syndrome to test parents or unborn children?
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.
Can a genetic counselor use a karyotype to identify a carrier of cystic fibrosis?
saddly and tragically :( no im terribly sorry
What genetic information can be identified easily with a karyotype?
The answer is,homologous chromosomes :) LOL hope that helped, even though i know it did ;)
A karyotype would be unable to Turner syndrome?
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.
What kind of analysis allows you to visualize an individual's chromosome composition?
karyotype analysis
What is An ordered display of an individuals chromosomes is called?
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.
A photo of the chromosomes in a dividing cell arranged by size is an?
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.
What information can be obtained about a fetus from a karyotype?
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.
How are cells obtained in order to create a karyotype?
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.
What is a picture that shows chromosomes arranged in pairs is a?
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.
How do you do a karyotype?
-Determine the gender of the individual. -To tell if 2 cells belong to the same species. -To detect the genetic abnormalities in Prenatal diagnosis.
What is metallurgical analysis?
Metallurgical analysis is the examination of metal, usually to detect cracks and weaknesses.
What is a picture of all the chromosomes in a cell?
This is known as a karyogram.
What is a picture called of all the chromosome in a cell?
A picture of chromosomes is called a "karyotype."
How is a karyotype created?
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
