Sample Exam #2 ( file)
... B. used to translate an mRNA into the amino acid sequence of a protein. C. the code geneticists use to let A stand for adenine, G for guanine, C for cytosine, and T for thymidine. D. sequences of one, two or three bases depending on how many amino acids are found in a protein. ...
... B. used to translate an mRNA into the amino acid sequence of a protein. C. the code geneticists use to let A stand for adenine, G for guanine, C for cytosine, and T for thymidine. D. sequences of one, two or three bases depending on how many amino acids are found in a protein. ...
Biology 12
... 5. The pH of blood is maintained at approximately 7.4 by a buffering system. What is the function of a buffer? Describe what could happen to hemoglobin (protein) if a buffering system was absent and the pH of blood became acidic? Buffer- resists changes in pH If blood were to become acidic hemoglob ...
... 5. The pH of blood is maintained at approximately 7.4 by a buffering system. What is the function of a buffer? Describe what could happen to hemoglobin (protein) if a buffering system was absent and the pH of blood became acidic? Buffer- resists changes in pH If blood were to become acidic hemoglob ...
Water
... as the mRNA is moved through the ribosome one codon at a time. (When completed, the polypeptide is released from the ribosome.) ...
... as the mRNA is moved through the ribosome one codon at a time. (When completed, the polypeptide is released from the ribosome.) ...
Biology 20
... 3. After you have broken down your breakfast items into simpler products. The chemical reactions that result in the building of more complex molecules are referred to as reactions. a) anabolic; b) catabolic; c) dehydration; d) none of these. 4. Three or four of the following statements concerning en ...
... 3. After you have broken down your breakfast items into simpler products. The chemical reactions that result in the building of more complex molecules are referred to as reactions. a) anabolic; b) catabolic; c) dehydration; d) none of these. 4. Three or four of the following statements concerning en ...
Introduction
... Plasma was separated from the blood cells by centrifugation at 1500 g for 10 minutes. The supernatant was then transferred to fresh tubes ensuring that the buffy coat remained intact. The plasma was then centrifuged at 16000 g for 10 minutes to remove any remaining cells, transferred into 2 ml Lo-Bi ...
... Plasma was separated from the blood cells by centrifugation at 1500 g for 10 minutes. The supernatant was then transferred to fresh tubes ensuring that the buffy coat remained intact. The plasma was then centrifuged at 16000 g for 10 minutes to remove any remaining cells, transferred into 2 ml Lo-Bi ...
CH-13 Sect 1
... 12. Is the following true or false? Making changes to the DNA code is similar to changing the code of a computer program. ____ 13. Scientists use their knowledge of the ___________________ of DNA and its ___________________ properties to study and change DNA molecules. 14. Explain how biologists get ...
... 12. Is the following true or false? Making changes to the DNA code is similar to changing the code of a computer program. ____ 13. Scientists use their knowledge of the ___________________ of DNA and its ___________________ properties to study and change DNA molecules. 14. Explain how biologists get ...
Document
... 3. What is the name of the DNA structure (shape)? 4. What are the building blocks of DNA? 5. This building block consists of three components. What are they? 6. Name (not just letter) the four nitrogen bases and how the pair. 7. The process that produces two new double helixes that are identical to ...
... 3. What is the name of the DNA structure (shape)? 4. What are the building blocks of DNA? 5. This building block consists of three components. What are they? 6. Name (not just letter) the four nitrogen bases and how the pair. 7. The process that produces two new double helixes that are identical to ...
生物化學小考(一) 範圍ch1~ch4
... (E) tryptophan 2. The ribosyl phosphate moiety needed for the synthesis of orotidylate, inosinate, and guanylate is provided most directly by: (A) 5-phosphoribosyl 1-pyrophosphate. (B) adenosine 5'-phosphate. (C) guanosine 5'-phosphate. (D) ribose 5-phosphate. (E) ribulose 5-phosphate. 3. A cell tha ...
... (E) tryptophan 2. The ribosyl phosphate moiety needed for the synthesis of orotidylate, inosinate, and guanylate is provided most directly by: (A) 5-phosphoribosyl 1-pyrophosphate. (B) adenosine 5'-phosphate. (C) guanosine 5'-phosphate. (D) ribose 5-phosphate. (E) ribulose 5-phosphate. 3. A cell tha ...
Biochem BIG IDEAS - Canvas by Instructure
... nucleotide, that determine the direction in which complementary nucleotides are added during DNA synthesis and the direction in which transcription occurs (from 5' to 3'). [See also 3.A.1] (See DNA unit) 2. Proteins have an amino (NH2) end and a carboxyl (COOH) end, and consist of a linear sequence ...
... nucleotide, that determine the direction in which complementary nucleotides are added during DNA synthesis and the direction in which transcription occurs (from 5' to 3'). [See also 3.A.1] (See DNA unit) 2. Proteins have an amino (NH2) end and a carboxyl (COOH) end, and consist of a linear sequence ...
PP-WEEK-12-CLASS
... Natural selection encourages passage of beneficial genes to future generations and discourages harmful or less valuable genes ...
... Natural selection encourages passage of beneficial genes to future generations and discourages harmful or less valuable genes ...
dna_notes - KScience
... Mutations are sometimes beneficial because they generate variability, which is the basis of natural selection. Mutations are more often deleterious because selection in a species has selected for the genome it now has and changes are therefore more likely to be less useful. Mutations can lead to sev ...
... Mutations are sometimes beneficial because they generate variability, which is the basis of natural selection. Mutations are more often deleterious because selection in a species has selected for the genome it now has and changes are therefore more likely to be less useful. Mutations can lead to sev ...
Chapters 19-21 review
... 11. Palindrome sequences on DNA that are recognized by restriction enzymes. ...
... 11. Palindrome sequences on DNA that are recognized by restriction enzymes. ...
BioSc 231 Exam 3 2005
... that would be produced by the RNA polymerase binding to this promoter (up to the end of the molecule). (4 points) ...
... that would be produced by the RNA polymerase binding to this promoter (up to the end of the molecule). (4 points) ...
Tools_and_Methods_of_Genetic_Engineering
... 4. problems: expensive to maintain, gene may be cut into several pieces Polymerase chain reaction (PCR) pg 391 1. method for making many copies of a specific segment of DNA 2. used in crime scene analysis when only tiny samples are present (ie. Drop of blood, a few hairs, skin under fingernails, etc ...
... 4. problems: expensive to maintain, gene may be cut into several pieces Polymerase chain reaction (PCR) pg 391 1. method for making many copies of a specific segment of DNA 2. used in crime scene analysis when only tiny samples are present (ie. Drop of blood, a few hairs, skin under fingernails, etc ...
CS691K Bioinformatics Kulp Lecture Notes #0 Molecular
... – Like DNA replication, DNA is opened into two single strands. – Using a ssDNA as a template, a complementary copy of RNA is synthesized for a small region of the genome (1000-100000nt) – The RNA is processed and transported (more about that in later ...
... – Like DNA replication, DNA is opened into two single strands. – Using a ssDNA as a template, a complementary copy of RNA is synthesized for a small region of the genome (1000-100000nt) – The RNA is processed and transported (more about that in later ...
Molecular Genetics
... • Recombinant DNA – Recombinant DNA is DNA that has been created artificially. DNA from two or more sources is incorporated into a single recombinant molecule. • Gel Electrophoresis – electric current is used to separate fragments of DNA; DNA fragments travel toward a negative charge ...
... • Recombinant DNA – Recombinant DNA is DNA that has been created artificially. DNA from two or more sources is incorporated into a single recombinant molecule. • Gel Electrophoresis – electric current is used to separate fragments of DNA; DNA fragments travel toward a negative charge ...
The Structure of DNA
... • Maurice Wilkins and Rosalind Franklin used Xray crystallography to study the structure of DNA. – In this technique, X-rays are diffracted as they passed through aligned fibers of purified DNA. – The diffraction pattern can be used to deduce the three-dimensional shape of molecules. • James Watson ...
... • Maurice Wilkins and Rosalind Franklin used Xray crystallography to study the structure of DNA. – In this technique, X-rays are diffracted as they passed through aligned fibers of purified DNA. – The diffraction pattern can be used to deduce the three-dimensional shape of molecules. • James Watson ...
Restriction Mapping Restriction Fragment Length Polymorphism
... These are 1 to 5 kb in length consisting of repeats 15 to 100 nucleotides in length and are identified by Southern analysis. 2. Microsatellite DNA ...
... These are 1 to 5 kb in length consisting of repeats 15 to 100 nucleotides in length and are identified by Southern analysis. 2. Microsatellite DNA ...
Chapter 9
... • Two nucleotide strands held together by hydrogen bonds • Hydrogen bonds between two strands are easily broken ...
... • Two nucleotide strands held together by hydrogen bonds • Hydrogen bonds between two strands are easily broken ...
Exam 1 Q2 Review Sheet
... 2. Describe the history concerning the discovery of the structure of DNA. Be sure to include the findings of Miescher, Levene, Chargaff, Franklin, Watson and Crick. 3. Know the structure of DNA and how to draw the various nucleotides. 4. Explain how DNA is replicated using diagrams and descriptions. ...
... 2. Describe the history concerning the discovery of the structure of DNA. Be sure to include the findings of Miescher, Levene, Chargaff, Franklin, Watson and Crick. 3. Know the structure of DNA and how to draw the various nucleotides. 4. Explain how DNA is replicated using diagrams and descriptions. ...
Hoku`s Slides
... Several coupled DNA and protein libraries are constructed, randomizing 3 base pairs and 5 contacting amino acids for each NNNGGAGGTTTCTCTGTAAA TGANNNGGTTTCTCTGTAAA ...
... Several coupled DNA and protein libraries are constructed, randomizing 3 base pairs and 5 contacting amino acids for each NNNGGAGGTTTCTCTGTAAA TGANNNGGTTTCTCTGTAAA ...
Deoxyribozyme
Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of catalyzing specific chemical reactions, similar to the action of other biological enzymes, such as proteins or ribozymes (enzymes composed of RNA).However, in contrast to the abundance of protein enzymes in biological systems and the discovery of biological ribozymes in the 1980s,there are no known naturally occurring deoxyribozymes.Deoxyribozymes should not be confused with DNA aptamers which are oligonucleotides that selectively bind a target ligand, but do not catalyze a subsequent chemical reaction.With the exception of ribozymes, nucleic acid molecules within cells primarily serve as storage of genetic information due to its ability to form complementary base pairs, which allows for high-fidelity copying and transfer of genetic information. In contrast, nucleic acid molecules are more limited in their catalytic ability, in comparison to protein enzymes, to just three types of interactions: hydrogen bonding, pi stacking, and metal-ion coordination. This is due to the limited number of functional groups of the nucleic acid monomers: while proteins are built from up to twenty different amino acids with various functional groups, nucleic acids are built from just four chemically similar nucleobases. In addition, DNA lacks the 2'-hydroxyl group found in RNA which limits the catalytic competency of deoxyribozymes even in comparison to ribozymes.In addition to the inherent inferiority of DNA catalytic activity, the apparent lack of naturally occurring deoxyribozymes may also be due to the primarily double-stranded conformation of DNA in biological systems which would limit its physical flexibility and ability to form tertiary structures, and so would drastically limit the ability of double-stranded DNA to act as a catalyst; though there are a few known instances of biological single-stranded DNA such as multicopy single-stranded DNA (msDNA), certain viral genomes, and the replication fork formed during DNA replication. Further structural differences between DNA and RNA may also play a role in the lack of biological deoxyribozymes, such as the additional methyl group of the DNA base thymidine compared to the RNA base uracil or the tendency of DNA to adopt the B-form helix while RNA tends to adopt the A-form helix. However, it has also been shown that DNA can form structures that RNA cannot, which suggests that, though there are differences in structures that each can form, neither is inherently more or less catalytic due to their possible structural motifs.