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Describe 20 . Upon Identification of thc DNA tcgularory squcncc the methods used to identify rhe location of sponsible for translaring given genc; You note that h t...

Question

Describe 20 . Upon Identification of thc DNA tcgularory squcncc the methods used to identify rhe location of sponsible for translaring given genc; You note that h transcription-control clements promoter-proximal entiched with CG scquences. Is thc corresponding gions of genes. Jikcly: bea highly expressed rranscript; What is the difference betwcen promoter-proximal cle- 21 , Namc four major classes of DNA-binding protelns rc ponsible controlling transctiption, Inde ment and distal enhancer: Wha

Describe 20 . Upon Identification of thc DNA tcgularory squcncc the methods used to identify rhe location of sponsible for translaring given genc; You note that h transcription-control clements promoter-proximal entiched with CG scquences. Is thc corresponding gions of genes. Jikcly: bea highly expressed rranscript; What is the difference betwcen promoter-proximal cle- 21 , Namc four major classes of DNA-binding protelns rc ponsible controlling transctiption, Inde ment and distal enhancer: What are the similarities: 10. thcir structural IcJtures; Describe rhe methods used identify the location of DNA-binding proteins in che regulatory = regions of genes.



Answers

Describe how DNA microarrays and DNA sequencing can be used to identify thedefective gene.

Here Assess described a different microsatellites mini satellite DNA. So, essentially, first of all, how can it be used? Teoh Identify individuals by offering your DNA fingerprinting. So basically, these are highly variable sequences which are different between individual. So we can basically look at, like, 12 different Lok I in order to see whether or not people have the same DNA. So essentially many satellite are going to be the most of highly variable sequence. Well, microsatellites here are just gonna be normal Variable sequence elements in DNA.

Problem 59 mm second restructure of 10 from Yeah. Holding off primary structure. Further folding of secondary structure gives tertiary structure. Mm hmm. Alpha helix, right handed quality structure and be to sit it seemed like structure. See reversible enzyme innovator not dime is the mm active side opens. I'm. And universal enjoying innovated. Did I miss the active site deep in Alafaya glucose hydroxy group below the first carbon in the ring. And in better glucose hydroxy group of. Of the ring. Mm Alpo 1 4 link is digestible in our body and Better one for link is not a digest table in our body uh in room temperature. Pat it's solid and while it is liquid G. Sunny. Okay saturated fatty acid content. Single bond and unsaturated fatty acid contained multiple bond between carbon atoms at forcefully beat content prospect group and Trackless role does not contend passport group I Trackless right. Is easter of practice it with alcohol glycerol. In wax it is easter off had decided with alcohol other than glycerol, a steroid content, poor ringing structure and access. Uh He stood off alcohol, jen and pat your chin, nucleotide content, hospital group and nuclear side, not content hospital group. Time, mean age mutilated. You're a cell and Mhm alpha helix is single polly peptide chain where double helix content to Chen and and deeper, little direction. There is an answer.

In this question, we have some scientific terms. We're going to match forms of their descriptions. So we have DNA fingerprint the T. V. Plasma. It you play, it assets hybridization. Again, mix restriction enzymes. Transgenic and GMOs. Let's have a look at our descriptions A having a foreign gene. This means that the organism is a transgenic organism. If it has a gene from a different species in it, he cuts DNA at a specific sequence Visa restriction enzymes. So we use these in a variety of biotechnologies. We use them to produce clothing back clones. We use them to um and sequencing to cut the power DNA fragments. Uh see a person's unique collection of short tandem repeats. This is your D. N. A fingerprint D. Base pairing of DNA. Or DNA and RNA from different sources. That is you click acids hybridization. Eat selecting desirable traits. This is for a human specific sub this is eugenics has great ethical issues in humans whereas we do it quite regularly in other species, for example, selective breeding in animals or plants for human benefit F genetically modified GMO genetically modified organisms. And she used in some gene transfers that SVT i plasmas very useful plasmids, but we often end up using um because it's just convenience.

The question here asked. What are the differences between DNA? My calories and protein so didn't relate a raise. You have thousands of bound single stranded DNA spots, while protein my, for raising this particular taste are basically going to have thousands of pounds amino acid sequences for proteins in this particular case.


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