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chapter 12 lecture slides
chapter 12 lecture slides

... • Refers to an allele which has more than one effect on the phenotype • Pleiotropic effects are difficult to predict, because a gene that affects one trait often performs other, unknown functions • This can be seen in human diseases such as cystic fibrosis or sickle cell anemia – Multiple symptoms c ...
sc-101769 (Page 1) - Santa Cruz Biotechnology, Inc.
sc-101769 (Page 1) - Santa Cruz Biotechnology, Inc.

... recommended: 1) Western Blotting: use goat anti-rabbit IgG-HRP: sc-2004 (dilution range: 1:2000-1:100,000) or Cruz Marker™ compatible goat antirabbit IgG-HRP: sc-2030 (dilution range: 1:2000-1:5000), Cruz Marker™ Molecular Weight Standards: sc-2035, TBS Blotto B Blocking Reagent: sc-2335 (use 50 mM ...
chapt12_lecture from text
chapt12_lecture from text

... • Refers to an allele which has more than one effect on the phenotype • Pleiotropic effects are difficult to predict, because a gene that affects one trait often performs other, unknown functions • This can be seen in human diseases such as cystic fibrosis or sickle cell anemia – Multiple symptoms c ...
Fruit-specific RNAi-mediated suppression of DET1 enhances
Fruit-specific RNAi-mediated suppression of DET1 enhances

... microarray pitfalls • cross-hybridization with related sequences • non-detection of sequence not included in the array • data handling is complex, therefore prone to human error (transformation, normalization, visualization, interpretation) • poor replication/experimental design • cDNA microarrays: ...
Communication - Dundee Life Sciences
Communication - Dundee Life Sciences

... maize mutant has resulted in the cloning of a gene, hcf106, encoding the first component (14). The Hcf106 protein is localized in the thylakoid membrane and appears to comprise a single transmembrane span with the bulk of the protein exposed to the stromal phase. There is now clear evidence for the ...
RESEARCH COMMUNICATION Ethnicity Greatly Influences the
RESEARCH COMMUNICATION Ethnicity Greatly Influences the

... DNA sequences of the human genome reveal that many genes are polymorphic. In coding or noncoding regions of a specific gene, there may be either a single base pair substitution of one nucleotide for another (SNPs) or a variable number of repeats of a short repetitive DNA sequence (VNTR). Gene-enviro ...
Mild dystrophic epidermolysis bullosa
Mild dystrophic epidermolysis bullosa

... Everyone has two copies of every gene, one inherited from their mother and one from their father. In DDEB a defect in one of those genes can lead to fragile skin and blistering, even though the other gene is ...
Identify differential APA usage from RNA-seq
Identify differential APA usage from RNA-seq

... experimental design exists: in this case only the correct pairs between control and treatment samples should be compared with the Fisher test; then their p-values can be combined following the Fisher method ([3]) because we have different independent tests on the same null hypothesis. For these situ ...
Part 1B Population and Community Dynamics - Science
Part 1B Population and Community Dynamics - Science

... the gradual change in allele frequencies of a population is called microevolution (microevolution: of a population, any change in allele frequencies resulting from mutation, genetic drift, gene flow, natural selection, or some combination of these) the Hardy-Weinberg principle can also be used to st ...
the Note
the Note

... Dihybrid cross: Di = TWO, so when two pairs of contrasting traits are crossed to determine the possible inheritance of the offspring. There will be 16 possible combinations that result from the cross – 2 possibilities from the male and 4 possibilities from the female (4 x 4 = 16). Filial generation: ...
found only in 2.25% of all muscle biopsies analyzed
found only in 2.25% of all muscle biopsies analyzed

... Pitié-Salpêtrière, Université Pierre et Marie Curie-Paris 6, Paris, France Dropped head syndrome is a common sight in several muscular disorders some of them associated with axial muscle involvement. However it can be a relevant feature in congenital muscular disorders in which lower limbs weakn ...
3D15 – BO0048 Code Questions Answers 1. Write the features of X
3D15 – BO0048 Code Questions Answers 1. Write the features of X

... b. All daughters of an affected male and a normal female are affected. c. Mating of affected females and normal males produce 50% the sons affected and 50% the daughters affected d. In the general population, females are more likely to be affected than males, even if the disease is not lethal in mal ...
Leukaemia Section t(7;14)(q21;q32) ERVWE1/IgH Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(7;14)(q21;q32) ERVWE1/IgH Atlas of Genetics and Cytogenetics in Oncology and Haematology

... Fusion protein ...
Supplementary Materials and Methods
Supplementary Materials and Methods

... methionine was removed and amino acid frequencies were plotted against each other, Figure 1.b. The largest increase in frequency of an amino acid is found in cysteines that account for 1.8% of amino acids in non-LSGs and 3.% of amino acids in LSGs (a 72.97% increase), Figure 1.b. Consistent with the ...
Bioinformatics in the post
Bioinformatics in the post

... genes expressed in specific cells or tissues. In this approach, BLAST is the method of choice to search for similarities against existing databases and to do all-against-all comparisons within the data set for identifying clusters of similar sequences. The mid-1990s saw the collection of another, qu ...
Mouse CNTF / Ciliary Neurotrophic Factor Protein (His Tag)
Mouse CNTF / Ciliary Neurotrophic Factor Protein (His Tag)

... Protein Construction: A DNA sequence encoding the mouse CNTF (NP_740756.1) (Ala2-Met198) was expressed with a polyhistidine tag at the N-terminus. ...
Summarizer PowerPoint - Butler Biology
Summarizer PowerPoint - Butler Biology

... • Involve problems with an entire chromosome, which may contain 1000’s of genes! ANEUPLOIDY: an abnormal number of chromosomes resulting from mistakes in meiois ...
Furry Family Pre
Furry Family Pre

... 6) In dogs, assume that black fur is dominant and brown fur is recessive. A male black dog and a female brown dog have a puppy, which is brown. Which most likely describes the genes of the parent dogs? a. Both parents carry the recessive genes b. The male parent carries the recessive gene, while the ...
Furry Family Pre
Furry Family Pre

... 6) In dogs, assume that black fur is dominant and brown fur is recessive. A male black dog and a female brown dog have a puppy, which is brown. Which most likely describes the genes of the parent dogs? a. Both parents carry the recessive genes b. The male parent carries the recessive gene, while the ...
Free Full Text ( Final Version , 673kb )
Free Full Text ( Final Version , 673kb )

... (31), with several millions of such potential markers spread over the genome (32). Because functionally relevant polymorphisms are expected to be associated with the disease, anonymous flanking SNPs in strong LD with such functional polymorphisms are also expected to be disease associated. Our marke ...
12864_2008_1659_MOESM3_ESM
12864_2008_1659_MOESM3_ESM

... branching of New World monkeys, which was followed by the integration of a MER9 LTR element into the C-terminus encoding part of what corresponds to the ORF of the parent gene. A segmental duplication prior to the branching of apes then yielded a second copy. Thereafter, one of the copies was interr ...
1. Which of the following is not a phenotypic description of allele
1. Which of the following is not a phenotypic description of allele

... Learning Objective: 03.02.04 Explain how continuous traits, like human height and skin color, are controlled by multiple alleles of ...
Assignment 2
Assignment 2

... than Monty chooses an empty box at random. And of course, two-thirds of the time that couldn’t be true. In the game, Monty can only open an unchosen empty box. In two out of three occasions the contestant is bound to choose just that — an empty box. In which case there’s only one box that Monty can ...
Communique of GTTAC Meeting 18 September 2003 and 28
Communique of GTTAC Meeting 18 September 2003 and 28

... (Monsanto) for the limited and controlled release of GM herbicide tolerant cotton (Roundup Ready® MON 88913) and herbicide tolerant/insect resistant cotton (Roundup Ready® MON 88913 /Bollgard II®). Monsanto proposes to conduct trials on 50 sites covering a total of 954 hectares, over three years, in ...
Communique of GTTAC Meeting 18 September 2003 and 28
Communique of GTTAC Meeting 18 September 2003 and 28

... (Monsanto) for the limited and controlled release of GM herbicide tolerant cotton (Roundup Ready® MON 88913) and herbicide tolerant/insect resistant cotton (Roundup Ready® MON 88913 /Bollgard II®). Monsanto proposes to conduct trials on 50 sites covering a total of 954 hectares, over three years, in ...
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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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