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The Bacillus subtilis lipoprotein LplA causes cell lysis
The Bacillus subtilis lipoprotein LplA causes cell lysis

transcription factors
transcription factors

... What determines the rate of transcription?  Transcription velocity is mostly constant, over one gene and from gene to gene.  Transcription length is determined by the gene. Thus …  (Molar) synthesis rate for transcription is controlled by gene length, number of RNAP's on the gene. Rates (Hargro ...
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... relationships, ChIP-chip data ... • Based on experimental data and computational ...
09. Paramecium Species Reading C
09. Paramecium Species Reading C

... one cell, two orifices, and thousands of hairy feet that project from its surface like beard stubble. Yet this seemingly primitive organism is capable of some surprisingly complex behaviors. It can swim 10 times the length of its body in one second, reproduce with and without the help of a partner, ...
Genetics
Genetics

... one complete set of chromosomes. In meiosis, homologous chromosomes line up and then move to separate daughter cells. Mitosis does not normally change the chromosome number of the original cell. This is not the case for meiosis, which reduces the chromosome number by half. Mitosis results in the pro ...
DNA Test For Fluffies - Norwich Terrier Club of America
DNA Test For Fluffies - Norwich Terrier Club of America

... Housley was casting about for a project when she came across a shelved study in Dr. Venta’s lab. It  had to do with the genetic factors governing hair length in dogs. She was intrigued.  “Many of the hair cycle genes have been identified and studied, just not in dogs.” And that’s how she  made an im ...
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Phenotype

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let-60(gf)
let-60(gf)

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AP Biology 042 – Biological Molecules Video
AP Biology 042 – Biological Molecules Video

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Heredity
Heredity

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materials - A New Kind of Science
materials - A New Kind of Science

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cs 253: principles of plant breeding
cs 253: principles of plant breeding

... epistasis 2. Duplicate gene action (15:1): a.k.a duplicate dominant epistasis 3. Recessive suppressors (13:3): a.k.a dominant and recessive epistasis 4. Additive gene action (9:6:1) 5. Dominant epistasis (12:3:1) 6. Recessive epistasis (9:3:4) ...
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Complete nucleotide sequence and genome organization of a

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Rhythmic Parsing of Sonified DNA and RNA Sequences
Rhythmic Parsing of Sonified DNA and RNA Sequences

... a framework as possible, so that it may be used as an analysis tool regardless of musical training or ability. In many fields where sonification could be of great benefit the very notion of using audio for analysis purposes is difficult enough to accept, and to this end any tools or principles devel ...
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bio ch14.3 ppt - Mrs. Graves Science

... • Genomes in microbes range from 400,000 to millions of base pairs and include from 400 to 9,300 genes. • Eukaryote genomes range from 100 million to more than 3 billion base pairs with 6,000 to 100,000 genes. • The human genome has about 30,000 genes. Some plants have more than 100,000 genes. ...
Unit 5: Genetics
Unit 5: Genetics

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Ab initio gene prediction
Ab initio gene prediction

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Application/registration document for work with biohazards and

... products or human tissues, primary human cell cultures, non-human primate blood or tissues, infected animals and animal tissues, toxins (bacterial, plant fungi, etc.), allergens, please answer questions 1-7 in this section. 1. Name of biohazardous agent. 2. Brief description of human diseases caused ...
Microbial Genomes - Griffith University
Microbial Genomes - Griffith University

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Chapter 1 Interactive Quiz

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Artificial gene synthesis

Artificial gene synthesis is a method in synthetic biology that is used to create artificial genes in the laboratory. Currently based on solid-phase DNA synthesis, it differs from molecular cloning and polymerase chain reaction (PCR) in that the user does not have to begin with preexisting DNA sequences. Therefore, it is possible to make a completely synthetic double-stranded DNA molecule with no apparent limits on either nucleotide sequence or size. The method has been used to generate functional bacterial or yeast chromosomes containing approximately one million base pairs. Recent research also suggests the possibility of creating novel nucleobase pairs in addition to the two base pairs in nature, which could greatly expand the possibility of expanding the genetic code.Synthesis of the first complete gene, a yeast tRNA, was demonstrated by Har Gobind Khorana and coworkers in 1972. Synthesis of the first peptide- and protein-coding genes was performed in the laboratories of Herbert Boyer and Alexander Markham, respectively.Commercial gene synthesis services are now available from numerous companies worldwide, some of which have built their business model around this task. Current gene synthesis approaches are most often based on a combination of organic chemistry and molecular biological techniques and entire genes may be synthesized ""de novo"", without the need for precursor template DNA. Gene synthesis has become an important tool in many fields of recombinant DNA technology including heterologous gene expression, vaccine development, gene therapy and molecular engineering. The synthesis of nucleic acid sequences is often more economical than classical cloning and mutagenesis procedures.
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