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dna and its structure
dna and its structure

... make sense! Mutations can lead to proteins that function poorly or not at all- this may or may not be of concern, it depends on what protein it is coding for. If there is a mutation in the hemoglobin of red blood cells that affects its shape, this could cause sickle cells that lead to blood clots (s ...
Fragmenting genomic DNA for cloning
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Week: Mar 10, 2014 Bio Willis,Locklear, Lester,Barber, Monday
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What is biochemistry?
What is biochemistry?

... In this example, eight separate protein samples were used (shown in the eight dark blue lanes). The middle lane shows the molecular mass marker. The bands have been stained with blue dye. Darker bands indicate the presence of a higher concentration of protein. Kilodaltons (kd) are units of mass used ...
Ecology
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Lab 4 Isolation of Total RNA from C. elegans
Lab 4 Isolation of Total RNA from C. elegans

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Bio290-08-Week 9
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View PDF of poster here
View PDF of poster here

... Immediately following the lysis step, detection of GC genomic DNA is carried out in silvered plate (Figure 3B), which have been shown to enhance the fluorescence signal. Detection of target genomic DNA is mediated by the complementary binding of two probes to the target sequence as shown in figure 2 ...
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ABOUT-BREAST-CANCER

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Illumina Solexa

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Why clone?

... develop age related conditions (arthritis, cancer, etc) at a younger age, most likely because of the shortening effect of DNA replication. Their DNA is “old” in essence, even though their bodies are not. Secondly, some gene control leads to surprising results in clones. An attempt to clone a calico ...
DNA Isolation From 300–450 mg Dried or 600–1200 mg Fresh Leaf
DNA Isolation From 300–450 mg Dried or 600–1200 mg Fresh Leaf

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... transcribed into mRNA and then translated (conversion of mRNA sequence into amino acids) into a protein. An individual’s environment, even in the womb, can influence these factors and permanently alter the expression of genes in the adult. Alterations in epigenetic mechanisms lead to development of ...
Pfu DNA Polymerase - G
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... Pfu DNA polymerase, derived from the hyperthermophilic archae Pyrococcus furiosus, has superior thermostability and proofreading properties compared to the other thermostable polymerase. Its molecular weight is 90 kD. It can amplify DNA target up to 2kb. The elongation velocity is 0.2~0.4kb/min (70~ ...
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Anth. 203 Lab, Exercise #1
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... Below is the base sequence for a small section of mitochondrial DNA (mtDNA) for 5 species of primate, as determined by Wesley Brown at U.C. Berkely. For the human and gibbon DNA codons, show the corresponding mRNA codons (on page 2) that would be synthesized during transcription and carry the messag ...
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Lecture 12
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... • The major steps involved in PCR are the following: 1. Double stranded DNA (ds DNA) or cDNA is denatured by heating at 9598℃. 2. Synthetic oligonucleotide primers with sequences complementary to target DNA are added in excess to the reaction mixture along with the ...
Recombination and Repair
Recombination and Repair

... (i) alignment of 2 homologous chromosomes (ii) introduction of breaks in DNAs (iii) formation of initial short regions of base pairing between the two recombining DNA molecules (strand invasion) (iv) movement of Holliday junctions by repeat melting and formation of base pair (branch migration) (v) c ...
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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.
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