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The genetic engineers toolkit
The genetic engineers toolkit

... • A lot of DNA consists of long stretches of repeated nucleotides . • These vary between individuals and can be separated using gel electrophoresis. • Dna profiling usually uses about 10 STR’s ...
Sample Prep for Denaturing PAGE of DNA
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Protein Synthesis - Helena High School
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... Use notes from the PowerPoint and complete the following questions. This will be the study guide for questions about transcription/translation. 1. DNA codes for what macromolecule? Provide three examples of proteins necessary in our bodies a. b. c. 2. Where is the code within the DNA molecule that p ...
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... G. restriction endonuclease H. reverse transcriptase ...
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... PCR was performed using primer pair P1 and P3 in one vial and P2 and P4 in another vial. The purified PCR products from the two vials were mixed and subjected to another round of PCR with primers P1 and P4. The final PCR product will correspond to a (A) 1.2 kb wild type DNA (B) 1.2 kb DNA with two p ...
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Genetic Technology

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... members. A common E1 appears in full length in Mnda. Truncated versions occur in Ifi202 and Ifi204. The intact sequence demonstrates 98-100% homology with one another. Ifi205 demonstrates 81-83% homology with the other family members. AIM2 E1 shares only 17% homology with Mnda E1. In real-time PCR d ...
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... The gene is a unit of hereditary information that holds the code for synthesis of proteins/polypeptides or traits/parts of a trait. The term ‘genome’ can refer to the entire genetic makeup of a cell, organism or species. Though most of the genome is non-coding, the coding regions (“genes”) are what ...
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August 31, 2016 - Iowa State University
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... b. Glycosidic Linkage – Nucleic Acids ...
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Real-time polymerase chain reaction



A real-time polymerase chain reaction is a laboratory technique of molecular biology based on the polymerase chain reaction (PCR). It monitors the amplification of a targeted DNA molecule during the PCR, i.e. in real-time, and not at its end, as in conventional PCR. Real-time PCR can be used quantitatively (Quantitative real-time PCR), semi-quantitatively, i.e. above/below a certain amount of DNA molecules (Semi quantitative real-time PCR) or qualitatively (Qualitative real-time PCR).Two common methods for the detection of PCR products in real-time PCR are: (1) non-specific fluorescent dyes that intercalate with any double-stranded DNA, and (2) sequence-specific DNA probes consisting of oligonucleotides that are labelled with a fluorescent reporter which permits detection only after hybridization of the probe with its complementary sequence.The Minimum Information for Publication of Quantitative Real-Time PCR Experiments (MIQE) guidelines propose that the abbreviation qPCR be used for quantitative real-time PCR and that RT-qPCR be used for reverse transcription–qPCR [1]. The acronym ""RT-PCR"" commonly denotes reverse transcription polymerase chain reaction and not real-time PCR, but not all authors adhere to this convention.
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