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Database Searches for similar sequences
Database Searches for similar sequences

Non-Mendelian inheritance
Non-Mendelian inheritance

... mtDNAs occur in all aerobic eukaryotic cells and generate energy for cell function by oxidative phosphorylation (OXPHOS) producing ATP. ...
No Slide Title
No Slide Title

... steps, exemplified in TBP/DNA complexes. At the first and last basepair steps of the TATA box, TBP kinks the DNA by inserting pairs of Phe side chains between the steps, and placing Leu and Pro side chains near the rim of the bases. QM calculations indicate that these side chains cannot discriminate ...
Evolutionary analysis of the female
Evolutionary analysis of the female

... Stein-Are Sæther4,9, Glenn-Peter Sætre4, Janos Török10 & Hans Ellegren1 ...
Meiosis - Montville.net
Meiosis - Montville.net

... ▪ Alleles are the variations of one gene –Ex: eye colors can brown, blue, green, hazel, etc…. ▪ You inherit one chromosome from each parent! ...
Mechanical opening of DNA by micromanipulation and force
Mechanical opening of DNA by micromanipulation and force

... vector DNA (7280 bp) is linearized by double digestion. One extremity is ligated to the PCR product, the other extremity is ligated to a short synthetic DNA fragment formed by hybridisation of two partial complementary oligonucleotides. This way we create two different types of linker arm molecules ...
lac
lac

... • Transformation is the alteration of a bacterial cell’s genotype by the uptake of naked, foreign DNA from the surrounding environment. • Many bacterial species have surface proteins that are specialized for the uptake of naked DNA. • These proteins recognize and transport only DNA from closely rel ...
Site-Directed Mutagenesis Using Oligonucleotide
Site-Directed Mutagenesis Using Oligonucleotide

Sources of Genetic Variation
Sources of Genetic Variation

... 1903 – Walter Sutton, the chromosomal theory of inheritance, chromosomes are the carriers of genetic information 1944 - Avery, MacLeod and McCarty show DNA was the genetic material 1953 - James Watson and Francis Crick discover the molecular structure of DNA: a double helix with base pairs of A + T ...
ANALYSIS OF MULTIPLE RESTRICTION FRAGMENT LENGTH
ANALYSIS OF MULTIPLE RESTRICTION FRAGMENT LENGTH

... probes and containing an insert of 14 .5 kb, termed XGSB 16.1, was restriction mapped (Fig. 1 B) . The Pvu II-Bam HI fragment, GB2PE, which contained neither human repeats nor CRI-1- and CRI-4-like sequences, hybridized to the 14.5-kb Bam HI fragment characteristic ofan S allele and to nonallelic fr ...
Cloning and Genetic Analysis of Six Pyrroloquinoline
Cloning and Genetic Analysis of Six Pyrroloquinoline

... non-pqqA mutants. R’5 1 was not a suitable tool for genetic analysis but, since it contains a large amount of M . organophilum DNA (about 100 kb), it was used as a source of DNA to build a genomic library in the cosmid pLA2917. Cosmid pM0550 (not shown), isolated from this library, retained the comp ...
genomic flux: genome evolution by gene loss and
genomic flux: genome evolution by gene loss and

... DNA may be introduced into bacterial genomes by many processes, including conjugation, bacteriophage-mediated transduction, and transformation. The general term recombination typically refers to the introduction of DNA from a conspecific cell, whereas horizontal genetic transfer or lateral genetic t ...
Generation and analysis of mutated clonal scFv Jiya George
Generation and analysis of mutated clonal scFv Jiya George

... showed interaction, however the antibody-antigen affinity was too weak for the virus neutralization assay. Hence, this project focused on the affinity maturation of the anti-R7V scFv fragments through random mutagenesis using the error prone (EP) PCR method. The EP PCR method generated two mutated a ...
Radiation Hybrid Mapping: A Somatic Cell Genetic Method for
Radiation Hybrid Mapping: A Somatic Cell Genetic Method for

PDF
PDF

... currently known. The retrotransposons, ERVs, and their remnant DNA sequences occupy approximately 40% of the mammalian genome and they have long been thought to be either “selfish” genes or useless “junk.” Is it thus the case that domestication events are very rare in mammals? Are there any domestica ...
Genome demethylation and imprinting in the endosperm
Genome demethylation and imprinting in the endosperm

... complete set of imprinted genes, the imprintome. One experimental approach to elucidate the imprintome is to cross different ecotypes, which creates a hybrid endosperm. RNA is isolated, converted to cDNA, and subjected to high-throughput sequencing. In this way, maternalderived transcripts and pater ...
Alteration by site-directed mutagenesis of the
Alteration by site-directed mutagenesis of the

... RecB mutagenesis RecB gene subcloning. The plasmid pDJ02 (11), containing a 13.5 kilo-base pair (kb) Smal-BamHI fragment encoding the recBCD genes, was digested with Xhol to produce a 3166 basepair (bp) fragment (nucleotides # 7,947—11,112 according to the numbering in (16,17)) containing part of th ...
A Dnmt2-like protein mediates DNA methylation in
A Dnmt2-like protein mediates DNA methylation in

... derivatized and analyzed by capillary electrophoresis as described previously (Stach et al., 2003). Samples from independent DNA preparations were measured at least three times, and the results were found to be strictly reproducible. To minimize the possibility of bacterial contaminations, fly food ...
Bioinformatics Course Notes (Ming Li)
Bioinformatics Course Notes (Ming Li)

... Given a gene sequence, BLAST or PH simply returns a bunch of alignments. Can we return a complete gene match? Idea: Combine PH with ExonHunter (Brejova, Brown, Li, Vinar, ISMB’2005): take the ab initio gene-finder (HMM) trained for the database genome, further train/bias it with the query gene model ...
x`*z`* _ _
x`*z`* _ _

... network for 10,000 times, calculating the proportion of times where the summarized connectivity between the known genes and novel candidates is larger than the observed one. If the empirical p-value is 0, it is set to 1e-5. Potential candidates were defined as the top 10 to 50 candidates ranked by F ...
The ROOT HAIRLESS 1 gene encodes a nuclear protein
The ROOT HAIRLESS 1 gene encodes a nuclear protein

... 1,4,7), from WS wild-type plants (lanes 2,5,8), and from Columbia wild-type plants (lanes 3,6,9) was digested with SalI (lanes 1,2,3), HindIII (lanes 4,5,6), and PstI (lanes 7,8,9). The 2-kb insert obtained in the left border plasmid rescue experiment was used as a probe. A second band hybridizing i ...
Practical General Microbiology Lab
Practical General Microbiology Lab

... Latex Test consists of latex particles coated with human fibrinogen and IgG. On mixing the latex reagent with colonies of staphylococci which have clumping factor or Protein A present, cross-linking will occur giving visible agglutination of the latex particles. Such agglutination will occur notably ...
Assaying … promoter activity
Assaying … promoter activity

... true breeding experiment. In this experiment, recombinant cells were grown at the non-permissive temperature in the absence of antibiotic selection for approximately 10 generations. Following this period, aliquots from this culture were plated onto selective (LB with 5 mg/L gentamicin) or non-select ...
Sequence Alignment
Sequence Alignment

... All life forms are related by common ancestry and descent. The construction of phylogenies provides explanations of the diversity seen in the natural world. Phylogenies can be based on morphological data, physiological data, molecular data or all three. Today, phylogenies are usually constructed usi ...
Health and Technology
Health and Technology

... Know what is meant by linked genes. Know the consequences of genes being linked. Understand the effect crossing over has on linked genes. Know the effect that crossing over has on distantly located genes. Know what cross-over values (COV) are. ...
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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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