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Biological Molecules Test Review Test covers carbohydrates, lipids
Biological Molecules Test Review Test covers carbohydrates, lipids

... J. List 4 groups of lipids and explain or describe their fnnction in living organisms. ...
a copy of the Candy DNA Replication
a copy of the Candy DNA Replication

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Transcription: Synthesizing RNA from DNA
Transcription: Synthesizing RNA from DNA

...  Promoter region is upstream for a specific gene. Promoter region contains two specific sets of nucleotide sequences. P252 Fig. 6.6  For each gene only ONE strand of the double-stranded DNA molecule is transcribed-this is called the ANTI-SENSE STRAND or TEMPLATE strand. The opposite strand that is ...
Codominance
Codominance

... make the antigens but do not secrete them in body fluids and are called “non-secreters.” Prior to the development of DNA identification analysis, secreter status was a key forensic tool. ...
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Slide 1

... 2. Translation – the mRNA, with the help of the ribosome, forms a chain of amino acids (eventually forming a protein) based on the information contained on the mRNA. ...
AP Biology Basics: From Gene to Protein
AP Biology Basics: From Gene to Protein

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An Overview of Protein Synthesis
An Overview of Protein Synthesis

...  The genetic code identifies the nucleotide combinations responsible for the each of the 20 known amino acids.  There are 4 bases which operate in sets of 3 (a triplet).= 43possible triplets of DNA =64 triplets  1 codon = 1 amino acid  The genetic code is degenerate - More than one codon codes f ...
Ingram 1957
Ingram 1957

... We owe to Pauling and his collaborators• the r ealization that sickle cell anremia is an example of an inherited 'molecular disease' and that it is due to an alteration in the structure of a large protein molecule, an alteration le~ding to a protein which is by all criteria still a h remoglobin. It ...
Cell Division and Inheritance
Cell Division and Inheritance

... ◦ Inherited genes – some people are more likely to get cancer because of their genetic make-up ◦ Frequency of exposure and the intensity of the exposure to cancer causing agents (up the odds) ◦ Infection by virus that inhibit the normal process of DNA replication or cell division ...
Reproduction and Development
Reproduction and Development

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Mutations and Genetic Variability 1. What is occurring in the diagram
Mutations and Genetic Variability 1. What is occurring in the diagram

... different chromosome. The type of chromosome translocation shown in the diagram is known as reciprocal translocation, which involves the exchange of material between two chromosomes. Reciprocal translocations are the most common type of translocation and do not result in a loss of genetic informatio ...
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DNA(Test 1)

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What is Willy Wonka famous for?

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Introduction to Evolution
Introduction to Evolution

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BIOLOGY-DNA replication, transcription, translation (DOC 98KB)

... Questions for each group to discuss and report back to the group OR briefly discuss as a whole class before starting the activity. ...
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Handout (Original Version).

... BACKGROUND: You have just completed an activity in which you made a cladogram showing the evolutionary relationships between seven organisms. The data used to draw that cladogram was based on shared characteristics that were inherited from their ancestors. Biochemical characteristics, like similarit ...
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Goal 3: The learner will develop an understanding of the continuity

... - linking amino acids in the proper order to make a functional protein -transcription- the process of copying DNA code onto mRNA. Transcription takes place in the nucleus. Following transcription, mRNA travels to the ribosome where translation takes place. -translation-synthesis of a polypeptide fro ...
Genetics 7 - Mr. Davros` Wiki
Genetics 7 - Mr. Davros` Wiki

Biotechnology and Genetic Engineering
Biotechnology and Genetic Engineering

... The Cry protein: mode of action • The Cry protein is made as an inactive protoxin • Conversion of the protoxin (e.g., 130 kDa) into the active toxin (e.g., 68 kDa) requires the combination of a slightly alkaline pH (7.5-8) and the action of a specific protease(s) found in the insect gut • The activ ...
Identification of a factor IX point mutation using SSCP analysis and
Identification of a factor IX point mutation using SSCP analysis and

... A molecular defect was localized to exon VI by single-strand conformation polymorphism (SSCP) analysis (2). To obtain sequence data the polymerase chain reaction (PCR, (3)) was used to symmetrically amplify a 250 bp fragment encompassing all of exon VI including both intron—exon splice junctions. Th ...
Eukaryotic Gene Control
Eukaryotic Gene Control

... conditions while facing changing external conditions ...
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I. GENETIC APPARATUS OF HUMAN CELL – SUPPORT OF

... Genome - the total complement of cellular DNA. In the cell could be identified nuclear genome (46 molecules of linear DNA) and mitochondrial genome (several identical molecules of circular DNA) Genotype - the total complement of genes contained in a cell or virus; commonly used in eukaryotes to refe ...
pdffile - UCI Math - University of California, Irvine
pdffile - UCI Math - University of California, Irvine

... ethics and social policy. Gene is a general term meaning, loosely, the physical entity transmitted from parent to offspring in reproduction that influences heredity traits, such as hair color, eye color, skin color, height, weight, and various aspects of behavior, which are also influenced by enviro ...
Document
Document

... Tay Sachs and lysosomes: human genetic disease -severe mental degradation -lysosomes lack one of the 40 required enzymes -results in a build up of fatty material on neurons -failure of nervous system communication -infantile form of the disease = death by 4 yrs -juvenile form = death from 5 to 15 yr ...
CH 8. DNA: The Universal Molecule of Life
CH 8. DNA: The Universal Molecule of Life

... Chromosome Mutations Chromosome mutation may result from:  Deletion (sections of a chromosome are missing and therefore some genes are missing) ...
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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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