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What else can I help you with?
How do you put DNA sample lengths 3500 in scientific notation?
In scientific notation 3500 is 3.5*10^3
What is Gap Closure methodology?
Its a technique adopted during DNA sequencing in which while joining the contigs we find whether there is any sequence present in between the contigs or not.If there is a sequence inbetween they re sequence the ends of the DNA.If not PCR is used to close the gaps.
In what type of real life situation would the extraction of DNA be useful?
Stem cells in general benefit from being injected with DNA. DNA is used in many crimes to determine who is guilty. For instance, a rape victimcould have skin underneath her fingernails that could be used to identify the perpetrator.
If a sample of DNA contained 20 percent cytosine what percentage of guanine would be in this sample and what percentage of adenine would be in the sample explain?
Umm I'll have to say that your a retard for not knowing it so tuff nubbs who ever made this is stupid because you spelled some words wrong.. The above answer is incorrect, and on a very low evolutionary rung. The correct answer is that with the amount of data provided, it is impossible to tell. If the answer isn't known, it is best to not answer.
Is PCR assays a qualitative or quantitative test?
PCR assays can be both qualitative and quantitative, depending on the method used. Qualitative PCR, often referred to as conventional PCR, detects the presence or absence of a specific DNA sequence. In contrast, quantitative PCR (qPCR or real-time PCR) measures the amount of DNA, providing information on the quantity of the target sequence in a sample. Thus, PCR can serve both purposes based on the specific assay design.
How does DNA fingerprinting relate to Poly Chain Reaction?
DNA fingerprinting uses variants in DNA sequences to create a unique profile for each individual, while the Polymerase Chain Reaction (PCR) is a technique used to amplify specific DNA sequences. PCR is commonly used in DNA fingerprinting to amplify regions of interest in the DNA sample before further analysis. This amplification step allows for better detection and characterization of DNA variations used in DNA fingerprinting.
What are the uses of DNA cloning in Forensic Science?
DNA cloning in forensic science is used to amplify and analyze DNA samples taken from crime scenes. This technique allows scientists to create copies of DNA fragments for further analysis, such as DNA profiling and identification of suspects. DNA cloning also helps in establishing genetic relationships and can be used to link suspects to crime scenes with high accuracy.
What is used to create a large sample of DNA for testing for a small sample of DNA?
A technique called polymerase chain reaction (PCR) is used to create a large sample of DNA from a small sample. PCR amplifies specific regions of DNA by making millions of copies, allowing for further analysis and testing on the amplified DNA.
A scientist wants to begin making a DNA fingerprint but she has only a very small DNA sample what should her next step be?
do a polymeras chain reaction (PCR). apex
Why was polymerase chain reaction developed?
makes more copies of a sample of DNA. apex
How do you determine if there is DNA present in your food?
To determine if there is DNA present in your food, you can use a simple test called a DNA extraction. This involves breaking down the food sample to release the DNA, then using a technique like PCR to amplify and detect the DNA molecules. This process can help identify the presence of DNA from plants, animals, or other organisms in the food.
How does polymere chain reaction relate to DNA fingerprinting?
PCR, or polymerase chain reaction, is a biochemical technique that can generate millions of copies of a template strand of DNA. The technique relies on the same enzymes that cells use to replicate DNA, however it is performed in a simple test tube using controlled cycles of heating and cooling. PCR has revolutionized the field of biotechnology, making it quick and inexpensive to replicate, or amplify, specific segments of DNA.
How is PCR used in conjunction with gel electrophoresis to analyze DNA samples?
Polymerase chain reaction (PCR) is used to amplify specific regions of DNA in a sample. Gel electrophoresis is then used to separate the amplified DNA fragments based on size. By comparing the resulting DNA bands on the gel, scientists can analyze and identify the DNA samples.
Process used to amplify small DNA samples?
Polymerase chain reaction (PCR) is a commonly used method to amplify small DNA samples. In PCR, the DNA sample is heated to separate the double-stranded DNA into single strands, then specific primers are added to flank the target DNA sequence. DNA polymerase then synthesizes new DNA strands complementary to the target sequence, resulting in exponential amplification of the DNA fragment.
Is polymerase chain reaction used to amplify DNA from a fossil a fetal cell or a virus?
The PCR reaction can be used to amplify DNA from all three sources mentioned. PCR relies on the use of short stretches of DNA that are 6 - 12 bases long to attach to the target DNA (the source where the DNA is coming from) so that the polymerase enzyme can make copies of the target DNA. As long as these primers are available (they can be commercially purchased in many cases), PCR can be carries out on fetal cell DNA and viral DNA. Fossil DNA however, may have undergone degradation. DNA has to be of a certain purity for PCR to work. If the fossil DNA had degraded or broken down, PCR cannot be carried out.
Is DNA Cloning used following procedures is used to amplify DNA in vitro?
polymerase chain reaction (PCR)
What does polymerase chain reaction enable scientist to make?
Polymerase chain reaction (PCR) enables scientists to make millions of copies of a specific DNA sequence in a short amount of time. This technique is commonly used in research, forensics, and medical diagnostics to amplify DNA for analysis.
