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... 6. What is the specific role of exonuclease-1 in this type of DNA repair? That is, which step does it accomplish? After a mismatch is identified and a nick introduced, EXO1 cuts out a section of the DNA strand containing the mismatched base. 7. How do E. coli distinguish between parental and newly r ...
Conservative replication
Conservative replication

... 2. The 15N become integrated into the bases, making the DNA in the bacteria heavier. 3. The bacteria grown with 15N was then moved into a medium with 14N. 4. Samples of bacteria were periodically taken out. 5. The DNA in these samples was extracted. ...
Biology 101 Lecture Quiz #12 Name
Biology 101 Lecture Quiz #12 Name

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AP Bio Ch 17 The Molecular Basis of Disease This chapter is only
AP Bio Ch 17 The Molecular Basis of Disease This chapter is only

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Genetics - California Science Teacher
Genetics - California Science Teacher

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Practice Question for Replication, Genetics and Biotechnology

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Prepare for gel electrophoresis

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Topic 12 DNA - Ms. Mogck`s Classroom

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Coloring DNA

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Genetic Engineering Paper Exercise

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forensics_by_students

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DNA structure and function

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How hair can reveal a history

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Study Guide Chap 6: DNA

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Jatropha genotyping In Gh Pu QR In Gh Pu QR 13 primer pairs

... commonly known as the physic nuts, contain up to 40% oil. The jatropha oil can be used directly as biofuel or can be converted into biodiesel for a more efficient performance. When raw or mixed jatropha oil is directly used in an automobile or even plane engines ...
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Genetic Engineering ​ Guied Notes

... 3. If host and foreign DNA have been cleaved by the same restriction enzyme, the ends can _ join_ together. 4. Gene cloning occurs- this cell continues to divide by __mitosis___ and __meiosis_____ this new foreign DNA (gene) as if it were its own ...
Genetic Engineering (and other cool molecular biology techniques)
Genetic Engineering (and other cool molecular biology techniques)

... PCR (polymerase chain reaction) • Specific sequence of DNA is amplified (copied many times) • Requires: – DNA template (contains your gene of interest) – Tac polymerase (a DNA polymerase that can work at high temperatures) – Nucleotides (to synthesize new DNA) – Primers (specific to the gene of int ...
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polymer of nucleotides = nitrogen base, pentose sugar, a phosphate

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molecular genetics unit review

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LEQ: How do we splice new genes into DNA?

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25/100 bp Mixed DNA Ladder DNA Molecular Weight Markers

... ● Description : 25/100 bp Mixed DNA Ladder is specially designed for determining the size of double strand DNA from 25 to 2,000 base pairs. The DNA Ladder consists of 17 double strand DNA fragments ranging in size from 25 to 200 bp in 25 bp increments, and additional fragments of 300, 400, 500, 600, ...
12.1 Notes - West Branch Schools
12.1 Notes - West Branch Schools

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DNA profiling



DNA profiling (also called DNA fingerprinting, DNA testing, or DNA typing) is a forensic technique used to identify individuals by characteristics of their DNA. A DNA profile is a small set of DNA variations that is very likely to be different in all unrelated individuals, thereby being as unique to individuals as are fingerprints (hence the alternate name for the technique). DNA profiling should not be confused with full genome sequencing. First developed and used in 1985, DNA profiling is used in, for example, parentage testing and criminal investigation, to identify a person or to place a person at a crime scene, techniques which are now employed globally in forensic science to facilitate police detective work and help clarify paternity and immigration disputes.Although 99.9% of human DNA sequences are the same in every person, enough of the DNA is different that it is possible to distinguish one individual from another, unless they are monozygotic (""identical"") twins. DNA profiling uses repetitive (""repeat"") sequences that are highly variable, called variable number tandem repeats (VNTRs), in particular short tandem repeats (STRs). VNTR loci are very similar between closely related humans, but are so variable that unrelated individuals are extremely unlikely to have the same VNTRs.The DNA profiling technique nowadays used is based on technology developed in 1988.
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