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Handout - 7 - Misc - Topics for discussion at June 2016
Handout - 7 - Misc - Topics for discussion at June 2016

... Historically, ACnc was used as a placeholder for the Property of Ordinal codes. A few years ago, we started transitioning to “Pr” as the Property for observations reported simply based on whether the analyte is present or not without being determined by a cut off value, and “Threshold” as the proper ...
Tutorial - QIAGEN Bioinformatics
Tutorial - QIAGEN Bioinformatics

... Figure 1: Toolbox folder structure after installation of the Bisulfite Sequencing plugin. Bisulfite sequencing is the use of bisulphite treatment of DNA to determine its pattern of methylation. DNA methylation was the first discovered epigenetic mark, and remains the most studied. Changes in cytosin ...
Archives of Microbiology
Archives of Microbiology

... of the VnfDG products are altered by this gene fusion, nor whether the unique addition of 21 nucleotides in the vnfDG fusion area of Anabaena sp. CH1 is of functional signiWcance. In a neighbor-joining analysis of all available deduced VnfDG sequences, those from cyanobacteria clustered next to thos ...
Cloning and Expression of Cellulosimicrobium cellulans β
Cloning and Expression of Cellulosimicrobium cellulans β

... for feeding at a later date [7]. Therefore, ensiled forages are the most commonly used feeds for ruminants all over the world [8]. Lactobacillus plantarum and other Lactobacillus species, Enterococcus faecium and Pediococcus species are most common silage inoculant bacteria and one or more of these ...
Early frameshift alleles of zebrafish tbx5a that fail to
Early frameshift alleles of zebrafish tbx5a that fail to

... alternatively that the existing hst allele and morpholino injections result in hypomorphic or dominant-negative conditions arising from truncated residual protein or lower protein concentration. The introduction of CRISPR-Cas9 for genome editing has provided the zebrafish field with an easily access ...
2 - cellbiochem.ca
2 - cellbiochem.ca

... • Antibiotic resistance gene: allow for selection for bacterial cells that have taken up the vector ...
Requirements for Human Medical Genome
Requirements for Human Medical Genome

A SNP in the ABCC11 gene is the determinant of human earwax type
A SNP in the ABCC11 gene is the determinant of human earwax type

... GG homozygotes at each of the three SNP loci (Table 1 and Supplementary Table 1 online). Among the SNPs, only rs17822931 is nonsynonymous (G180R); rs6500380 does not create any splicing sites nor affect splicing factor binding motifs or known promoter sequences, and ss49784070 is located within the ...
Mycobacterium kyorinense sp. nov., a novel, slow
Mycobacterium kyorinense sp. nov., a novel, slow

... Sequence analysis revealed that the 16S rRNA gene sequence of the newly identified mycobacterium was closest to that of M. celatum ATCC 51130 (type 2) with 18 base mismatches out of 1469 bp (98.8 % identity). It was also highly similar to that of M. celatum NCTC 12882 (type 3) with 25 base mismatche ...
DNA Sequencing (cont.) - A computational tour of the human genome
DNA Sequencing (cont.) - A computational tour of the human genome

... Repeats, errors, and contig lengths • Repeats shorter than read length are easily resolved  Read that spans across a repeat disambiguates order of flanking regions ...
the PDF file
the PDF file

... Is made of DNA, the basic genetic material ...
Plant Functional Genomics Plant Functional Genomics
Plant Functional Genomics Plant Functional Genomics

... and E. coli as the host, making library construction and subsequent downstream procedures efficient and easy to perform. Recombinant DNA inserts up to 200 kb can be efficiently cloned and stably maintained in E. coli. Although the insert size cloning capacity is much lower than that of the YAC syste ...
Comparative sequence analysis of the long repeat regions and
Comparative sequence analysis of the long repeat regions and

Reassignment of Drosophila willistoni Genome Scaffolds to
Reassignment of Drosophila willistoni Genome Scaffolds to

... (Pará, Brazil), but some (e.g., bw and hk) were generated in X-rayed cultures from strains of a different origin. The eye-color mutant brown (bw) was located at one end of the chromosome and was considered the starting point of the genetic map. However, Spassky and Dozhansky (1950) gave no indicatio ...
High-Level Expression in Escherichia coli of Alkaline Phosphatase
High-Level Expression in Escherichia coli of Alkaline Phosphatase

... stable at temperatures above 80oC, activated by Mg2+, and inhibited by Zn2+. In contrast, Zn2+ is essential for the activity of E. coli APase [1, 2, 7]. The gene encoding Tca APase was recently cloned into E. coli and the primary structure was deduced from its nucleotide sequence [9]. Like E. coli e ...
Transformation Lab - Towson University
Transformation Lab - Towson University

... transformation, bacteria take up exogenous (foreign) DNA and produce the genetic products (proteins) encoded in the foreign DNA. Transformation enables inexpensive and reliable production of important medical products such as insulin, human growth hormone, and other replacement hormone and gene ther ...
The dystrophin / utrophin homologues in Drosophila and in sea urchin
The dystrophin / utrophin homologues in Drosophila and in sea urchin

... sequence identity with dystrophin were characterized. Utrophin (DRP1) is encoded by an autosomal gene and consists of all four domains of dystrophin. At the amino acid level the two proteins show ,51% identity. The exon/intron structures of the two genes are also very similar (Love et al., 1989; Pea ...
Evidence for Variable Selective Pressures at a
Evidence for Variable Selective Pressures at a

... replication are still unknown. In this manuscript, control region and D loop will not be used as synonyms. The increasing amount of available sequences revealed a similar control region structural organization across mammals, with size variation ranging between 880 and 1400 bp (Sbisa et al. 1997). O ...
A rapid and specific PCR–ELISA for detecting Salmonella typhi
A rapid and specific PCR–ELISA for detecting Salmonella typhi

A novel arginine substitution mutation in 1A domain and a novel 27
A novel arginine substitution mutation in 1A domain and a novel 27

... previous evidence of family history of disease before the proband (II-1, marked by arrow). The mutation R135S created a novel restriction enzyme site (Blp I). Upon digestion, the PCR product was visualised as two distinct bands. Unaffected family members and 50 control individuals produced a single ...
Protein Sequence Alignment and Database Searching
Protein Sequence Alignment and Database Searching

Adherin - Semantic Scholar
Adherin - Semantic Scholar

... how the adherin proteins (Table 1) regulate diverse chromosomal functions and development. Adherin functions were originally revealed by genetic mutations in fungi: the rad9-1 adherin mutant of the mushroom Coprinus cinereus is defective in meiotic DNA repair, chromatid cohesin and homolog pairing [ ...
Positive and Negative Selection on Noncoding
Positive and Negative Selection on Noncoding

... polymorphism data for 78 genes from 15 wild-caught M. m. castaneus individuals and divergence to a closely related species, Mus famulus. We find high levels of nucleotide diversity and moderate levels of selective constraint in upstream and downstream regions compared with nonsynonymous sites of pro ...
Educational Technology Overview - Bee-Man
Educational Technology Overview - Bee-Man

... Strands of RNA or single-stranded DNA that have been labeled with a radioactive element or fluorescent dye and that is used to bind with and identify a specific gene in genetic engineering. Human Genome Project: A research effort to sequence and locate the entire collection of genes in human cells. ...
Locus in Salmonid Fishes Comparative Genome Analysis of the
Locus in Salmonid Fishes Comparative Genome Analysis of the

... Box bearing genes (SOX genes) that have major regulatory ...
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Genome editing

Genome editing, or genome editing with engineered nucleases (GEEN) is a type of genetic engineering in which DNA is inserted, replaced, or removed from a genome using artificially engineered nucleases, or ""molecular scissors."" The nucleases create specific double-stranded break (DSBs) at desired locations in the genome, and harness the cell’s endogenous mechanisms to repair the induced break by natural processes of homologous recombination (HR) and nonhomologous end-joining (NHEJ). There are currently four families of engineered nucleases being used: Zinc finger nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), the CRISPR/Cas system, and engineered meganuclease re-engineered homing endonucleases.It is commonly practiced in genetic analysis that in order to understand the function of a gene or a protein function one interferes with it in a sequence-specific way and monitors its effects on the organism. However, in some organisms it is difficult or impossible to perform site-specific mutagenesis, and therefore more indirect methods have to be used, such as silencing the gene of interest by short RNA interference (siRNA) . Yet gene disruption by siRNA can be variable and incomplete. Genome editing with nucleases such as ZFN is different from siRNA in that the engineered nuclease is able to modify DNA-binding specificity and therefore can in principle cut any targeted position in the genome, and introduce modification of the endogenous sequences for genes that are impossible to specifically target by conventional RNAi. Furthermore, the specificity of ZFNs and TALENs are enhanced as two ZFNs are required in the recognition of their portion of the target and subsequently direct to the neighboring sequences.It was chosen by Nature Methods as the 2011 Method of the Year.
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