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Possibilities and Limitations of Genetic Engineering
Possibilities and Limitations of Genetic Engineering

... such as tolerance to abiotic and biotic stresses, forage quality, and herbicide resistance. Alfalfa is also being engineered to produce novel compounds for industrial and diagnostic purposes. This research will likely lead to the production of improved cultivars, as well as new uses for alfalfa. INT ...
Gene conversion and purifying selection shape nucleotide variation
Gene conversion and purifying selection shape nucleotide variation

... sequenced only one strand for other samples if there was no nucleotide difference from the ones for which both strands were sequenced. When we found nucleotide differences in two or more individuals at the same site, we sequenced both strands of at least one of the samples to confirm the variation. ...
Two Genes with Similarity to Bacterial Response Regulators Are
Two Genes with Similarity to Bacterial Response Regulators Are

... that predicted from our sequence. The predicted IBC7 protein is 72% identical and 91% similar to IBC6 across the response regulator domain (Figure 1C). In addition to the putative response regulator domain, the predicted IBC7 amino acid sequence contains a 10-kD C-terminal extension that has a Ser/P ...
Biomart/ GENOME ALIGNMENT III
Biomart/ GENOME ALIGNMENT III

... and the mouse sequence. Even in remote organisms such as fugu and zebrafish some of the human exons are conserved. Between rat and mouse and human in the region 1000 bp upstream of the first exons parts of the sequence are conserved as well. These might correspond to the regulatory motifs, responsib ...
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Methods of Protein Analysis
Methods of Protein Analysis

attachment 2 - Food Standards Australia New Zealand
attachment 2 - Food Standards Australia New Zealand

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The chromatin remodelling factor Brg1 interacts with catenin to

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GROW`N`GLOW: THE ACE1 TWO-HYBRID

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RT2 Profiler PCR Arrays: Pathway-focused gene
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... Abstract: This paper evaluates the performance of the newest technique for monitoring the expression of a panel of pathway- or disease-specific genes: the RT2 Profiler PCR Array System. The RT2 Profiler PCR Array System combines the quantitative performance of SYBR® Green real-time PCR with the mult ...
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Expression of phosphofructokinase in Neisseria meningitidis

... demand of the cell increases (Blangy et al., 1968). The ATPPFK described above (PFK-1) is broadly distributed in Eukaryota and Bacteria, as indicated by homologous protein sequences and biochemical evidence (Bapteste et al., 2003), and is encoded by the pfkA gene. A second type of ATP-PFK enzyme (PF ...
Horizontal Gene Transfer between Bacteria
Horizontal Gene Transfer between Bacteria

... ‘Genetic material’ refers to any fraction of the genome (DNA or RNA), usually a gene or part thereof, which can include coding and/or non-coding sequences. ‘Organism’, as used here, includes cellular organism or replication competent virus. ‘Reproduction’ refers to the generation of offspring sexual ...
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Tumor metastasis-associated human MTA1 gene and its MTA1

... and it is thought that its major function is associated with its nuclear location [14, 15]. Recently, two groups reported that nucleosome remodeling histone deacetylase complex (NuRD complex), which is involved in chromatin remodeling, contains MTA1 protein or a MTA1-related protein (MTA2) [16, 17]. ...
Structures in the lac
Structures in the lac

... 1) Repressor site: broken, doesn't allow the production of the lac repressor 2) Operator: broken, won't allow binding of the repressor 3) Promotor: broken, won't allow binding of the RNA polymerase 4) LacY: broken, doesn't produce the B-galactoside permease to transport lactose into the cell 5) LacZ ...
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7.1 Introduction

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The causal meaning of Fisher`s average effect
The causal meaning of Fisher`s average effect

... meant by the quoted definition of the average effect was as follows. We randomly sample a zygote immediately after fertilization but before the onset of any developmental events. If the zygote’s genotype contains a gene of a certain allelic type, say A1 , we change it to A2 . This experimental interve ...
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Gene nomenclature

Gene nomenclature is the scientific naming of genes, the units of heredity in living organisms. An international committee published recommendations for genetic symbols and nomenclature in 1957. The need to develop formal guidelines for human gene names and symbols was recognized in the 1960s and full guidelines were issued in 1979 (Edinburgh Human Genome Meeting). Several other species-specific research communities (e.g., Drosophila, mouse) have adopted nomenclature standards, as well, and have published them on the relevant model organism websites and in scientific journals, including the Trends in Genetics Genetic Nomenclature Guide. Scientists familiar with a particular gene family may work together to revise the nomenclature for the entire set of genes when new information becomes available. For many genes and their corresponding proteins, an assortment of alternate names is in use across the scientific literature and public biological databases, posing a challenge to effective organization and exchange of biological information. Standardization of nomenclature thus tries to achieve the benefits of vocabulary control and bibliographic control, although adherence is voluntary. The advent of the information age has brought gene ontology, which in some ways is a next step of gene nomenclature, because it aims to unify the representation of gene and gene product attributes across all species.Gene nomenclature and protein nomenclature are not separate endeavors; they are aspects of the same whole. Any name or symbol used for a protein can potentially also be used for the gene that encodes it, and vice versa. But owing to the nature of how science has developed (with knowledge being uncovered bit by bit over decades), proteins and their corresponding genes have not always been discovered simultaneously (and not always physiologically understood when discovered), which is the largest reason why protein and gene names do not always match, or why scientists tend to favor one symbol or name for the protein and another for the gene. Another reason is that many of the mechanisms of life are the same or very similar across species, genera, orders, and phyla, so that a given protein may be produced in many kinds of organisms; and thus scientists naturally often use the same symbol and name for a given protein in one species (for example, mice) as in another species (for example, humans). Regarding the first duality (same symbol and name for gene or protein), the context usually makes the sense clear to scientific readers, and the nomenclatural systems also provide for some specificity by using italic for a symbol when the gene is meant and plain (roman) for when the protein is meant. Regarding the second duality (a given protein is endogenous in many kinds of organisms), the nomenclatural systems also provide for at least human-versus-nonhuman specificity by using different capitalization, although scientists often ignore this distinction, given that it is often biologically irrelevant.Also owing to the nature of how scientific knowledge has unfolded, proteins and their corresponding genes often have several names and symbols that are synonymous. Some of the earlier ones may be deprecated in favor of newer ones, although such deprecation is voluntary. Some older names and symbols live on simply because they have been widely used in the scientific literature (including before the newer ones were coined) and are well established among users.
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