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Large-Scale Purification Of Plasmids pRIT4501 and - RIT
Large-Scale Purification Of Plasmids pRIT4501 and - RIT

... Now that you have identified your two recombinant plasmids, you need to produce large-scale preparations of each so that you can study them further. To do this, you will prepare lysates of 500 ml cultures and purify the DNA by density gradient centrifugation. Although you could have used the alkalin ...
Open full article - About the Conference MendelNet 2016
Open full article - About the Conference MendelNet 2016

... However, the experiment was carried out in very early seedling stage and it is not exactly known whether they included monoecious plants, in which stage of onthogenesis the development of male phenotype really begins and what mechanisms are underlying it. Comparison with SCAR markers The same set an ...
Epigenetics and Inheritance
Epigenetics and Inheritance

... not) when the DNA is being copied during cell division and adding a methyl group to the newly made side of the DNA. It also regulates reactions involving proteins and lipids and controls the processing of chemicals that relay signals in the nervous system (neurotransmitters). Mouse knockouts of the ...
emboj7601986-sup
emboj7601986-sup

The Canine Genome: Discoveries, Applications - Encompass
The Canine Genome: Discoveries, Applications - Encompass

... varieties, breeds, and even species. The phenotype can include both physical and behavioral traits, such as herding, pointing, and running. The genetic information is encoded in the sequence of nucleotides found in DNA. Any variation in the order of adenine, thymine, cytosine, or guanine provides fo ...
Gene Patents in India: Gauging Policy by an Analysis of the
Gene Patents in India: Gauging Policy by an Analysis of the

... inventions.7 This draft stated that any living entity of artificial origin such as transgenic animals and plants and any part thereof are not patentable. The living entities of natural origin such as animals, plants, in whole or any parts thereof, plant varieties, seeds, species and genes8 are not c ...
Brian Yu - Comparison of Microarrayc and RNA-Seq Analysis Methods for Single Cell Transcriptiomics
Brian Yu - Comparison of Microarrayc and RNA-Seq Analysis Methods for Single Cell Transcriptiomics

... Currently, gene expression microarrays and RNA-seq are two popular ways of extracting single cell transcriptome data. Both methods allow high throughput analysis of many cells and gene targets. Developed in the 1990s, high density microarrays are more mature than deep sequencing technologies. With a ...
Fine mapping of Restorer-of-fertility in pepper (Capsicum
Fine mapping of Restorer-of-fertility in pepper (Capsicum

... (http://peppergenome.snu.ac.kr). Version 0.83 contigs and version 0.9 scaffolds were used to develop and anchor markers, respectively. Later, scaffold sequences included in the DNA region co-segregating with Rf were replaced with up-to-date versions of these chromosome sequences (version 1.55) (Kim ...
Identification of R-Gene Homologous DNA Fragments Genetically
Identification of R-Gene Homologous DNA Fragments Genetically

... Col×Ler population of recombinant inbred lines (RILs) available for mapping (Lister and Dean 1993). For the PCR, degenerate primers RG1 and RG2 were used whose sequences were based on the conserved P-loop and domain 5 region of the NBS in the N, L6, and RPS2 R-genes from tobacco, flax, and A. thalia ...
OSIRIS: a tool for retrieving literature about sequence variants
OSIRIS: a tool for retrieving literature about sequence variants

... Received on April 19, 2006; revised on July 13, 2006; accepted on July 28, 2006 Advance Access publication July 31, 2006 Associate Editor: Alvis Brazma ABSTRACT Summary: Sequence variants, in particular single nucleotide polymorphisms (SNPs), are key elements for the identification of genes associat ...
MS-SCI-LS-Unit 2 -- Chapter 6- Modern Genetics
MS-SCI-LS-Unit 2 -- Chapter 6- Modern Genetics

... the sex chromosomes when egg and sperm cells form? Since both of a female's sex chromosomes are X chromosomes, all eggs carry one X chromosome. Males, however, have two different sex chromosomes. Therefore, half of a male's sperm cells carry an X chromosome, while half carry a Y chromosome. When a s ...
Cis-regulatory mutations in human disease
Cis-regulatory mutations in human disease

... that does not encode for protein [2]. A flurry of papers stemming, in large part, from two broad areas of investigation has recently made a significant impact on the field of gene regulation. The first revolves around the genetic basis of human disease. Fueled by the power of linkage and genome-wide ...
Processivity of DNA polymerases: two mechanisms, one goal
Processivity of DNA polymerases: two mechanisms, one goal

... http://biomednet.com/elecref/0969212600600121 © Current Biology Ltd ISSN 0969-2126 ...
Molecular study of a consanguineous family with autosomal
Molecular study of a consanguineous family with autosomal

... In developed countries, medical aspects of human genetic disorders have become more prominent as nonhereditary causes of ill health or early death, such as infectious diseases or nutritional deficiency, have declined [9]. Online Mendelian Inheritance in Man (OMIM), an authoritative database of inher ...
testis formation. gene(s) - Journal of Medical Genetics
testis formation. gene(s) - Journal of Medical Genetics

... (fig 1). Testicular development and ovarian germ cells were absent. In the extragonadal organs, severe necrotising vasculitis characteristic of polyarteritis nodosa was observed. ...
Genome-wide DNA replication profile for
Genome-wide DNA replication profile for

... that require proximity to heterochromatin for proper regulation12 and therefore have been defined as heterochromatic genes. These genes, however, reside in β-heterochromatin, which, unlike the centromeric α-heterochromatin, does not possess highly repetitive DNA and has a euchromatin-like gene densi ...
MUTATIONS
MUTATIONS

... NON-SYNONYMOUS MUTATIONS :MISSENSE  A single base pair substitution can result in coding for a different amino acid and the synthesis of an altered protein, a so-called missense mutation.  Non-conservative substitution: If mutation coding for an amino acid which is chemically dissimilar such dif ...
MCB 421-2006: Homologous Recombination
MCB 421-2006: Homologous Recombination

... RecG and RUV proteins 1) work at the stage of recombinational repair that is different from the stage at which RecBC and RecFOR work; 2) define the two alternative pathways of the stage. If we combine the results of epistatic analysis with the previous results of the substrate analysis above, we arr ...
Introduction to pGLO lab
Introduction to pGLO lab

... jellyfish could be used to report when a protein was being made in a cell. Proteins are extremely small and cannot be seen, even under an electron microscope. However if one could somehow link GFP to a specific protein, for example hemoglobin, one would be able to see the green fluorescence of the G ...
ods of time, until activated b), a activated, the I`irtrl DNA hiiacks the
ods of time, until activated b), a activated, the I`irtrl DNA hiiacks the

... another. What was not understood was the specific arrangement of atoms that gave DNA its unique properties-the c-aP19lty to store genetic information, copy it, and pass it from gereration to generati.on. However, only one year after Hershey and Chase published their results, scientists figured out t ...
Introduction to pGLO lab
Introduction to pGLO lab

... jellyfish could be used to report when a protein was being made in a cell. Proteins are extremely small and cannot be seen, even under an electron microscope. However if one could somehow link GFP to a specific protein, for example hemoglobin, one would be able to see the green fluorescence of the G ...
Rare genomic changes and mitochondrial sequences
Rare genomic changes and mitochondrial sequences

... have also proven to be phylogenetically informative within some groups, such as ticks (Murrell et al., 2003) and spiders (Masta and Boore, 2008). Besides potentially providing new types of genome structure characters for making phylogenetic inferences, mitochondrial genomes provide a rich source of ...
The mitochondrial genome of the soybean cyst nematode
The mitochondrial genome of the soybean cyst nematode

... final incubation at 68 °C for 12 min is included, to complete the synthesis of any partial amplicons. In the second round of the step-out procedure, two primers were used. One of these was the species-specific primer used in round 1, while the second was another species-specific primer designed from ...
02/04
02/04

... RNA polymerase recognizes signals for chain termination. (1) Intrinsic: Termination site on template DNA consists of GC-rich sequences followed by A’s. Intramolecular hydrogen bonding causes formation of hairpin loop. ...
Surveying Saccharomyces Genomes to Identify Functional Elements
Surveying Saccharomyces Genomes to Identify Functional Elements

... sequences within proteins, but has been less useful for identifying functional sequence elements in nonprotein-coding DNA because the relatively rapid rate of change of nonprotein-coding sequences and the relative simplicity of non-coding regulatory sequence elements necessitates the comparison of s ...
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Genomics

Genomics is a discipline in genetics that applies recombinant DNA, DNA sequencing methods, and bioinformatics to sequence, assemble, and analyze the function and structure of genomes (the complete set of DNA within a single cell of an organism). Advances in genomics have triggered a revolution in discovery-based research to understand even the most complex biological systems such as the brain. The field includes efforts to determine the entire DNA sequence of organisms and fine-scale genetic mapping. The field also includes studies of intragenomic phenomena such as heterosis, epistasis, pleiotropy and other interactions between loci and alleles within the genome. In contrast, the investigation of the roles and functions of single genes is a primary focus of molecular biology or genetics and is a common topic of modern medical and biological research. Research of single genes does not fall into the definition of genomics unless the aim of this genetic, pathway, and functional information analysis is to elucidate its effect on, place in, and response to the entire genome's networks.
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