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Ch15 review regbio
Ch15 review regbio

Review Worksheet Exam 3
Review Worksheet Exam 3

... 5. From one of the daughter cells, show the production of gametes via meiosis (you do not need to show the steps of meiosis, just the outcome in terms of chromosome 8 in the gametes.) 6. Label all the cells with diploid (2n) or haploid (n) and indicate whether they are somatic cells or gametes. Chec ...
DNA Technology PPT
DNA Technology PPT

... – These cuts produce pieces of DNA called restriction fragments • That may have “sticky ends” that are important – DNA ligase pastes the DNA fragments together – The result is recombinant DNA ...
Production of Turnip yellow mosaic virus Capsids: The Future in
Production of Turnip yellow mosaic virus Capsids: The Future in

...  To develop protein nanospheres as a protective and nutritious delivery vehicle for zinc ...
Point Mutation Detection
Point Mutation Detection

... Patient cells are necessary to initiate molecular genetic analysis. Typically, patient material is a blood sample, biopsy specimen, and amniotic fluid or chorionic villus sample, though any nucleated cell sample is acceptable. Using blood as an example, total genomic DNA is extracted and the DNA is ...
Applied Biosystems: Celebrating 25 Years of Advancing Science
Applied Biosystems: Celebrating 25 Years of Advancing Science

Pl Path 111- Variability in Plant Pathogens
Pl Path 111- Variability in Plant Pathogens

... • Parasexualism is the process by which genetic recombination can occur with in fungal heterokaryon • In heterokaryotic fungal mycelium there is always the opportunity for dissimilar nuclei to fuse and produce diploids or what is known as mitotic recombination. Mitotic recombination can then occur p ...
Page 1 Name KEY_______________________ Genetics C3032
Page 1 Name KEY_______________________ Genetics C3032

... deletion in his DNA for a cloned gene (assume that you know the sequence of the gene and know where the missing DNA has come from; the answer should not use sequencing). ...
Hemoglobin Beta
Hemoglobin Beta

The Spurious Foundation of Genetic Engineering
The Spurious Foundation of Genetic Engineering

... transferred to the next genetic carrier - messenger RNA. A specialized group of fifty to sixty proteins, together with five small molecules of RNA - known as a "spliceosome" - assembles at sites along the length of the messenger RNA, where it cuts apart various segments of the messenger RNA. Certain ...
Chromosomal Theory of Inheritance
Chromosomal Theory of Inheritance

...  DNA sequencing has depended on advances in technology, starting with making recombinant DNA  In recombinant DNA, nucleotide sequences from two different sources, , are combined in vitro into the same DNA molecule  Methods for making recombinant DNA are central to , the direct manipulation of gen ...
Supplemental Materials and Methods (doc 44K)
Supplemental Materials and Methods (doc 44K)

... were performed in 20 µl reaction mixtures that were composed of SensiMix Plus SYBR Green & Fluorescein (Bioline GmbH, Luckenwalde, Germany), 1.2 µl 50 mM MgCl2 (Bioline GmbH), 150 ng/µl bovine serum albumin, 0.2 - 1.6 pM of each primers (Biomers, Ulm, Germany), 5 µl of template DNA and sterilized de ...
What is the genetic basis of complex traits? One of the most
What is the genetic basis of complex traits? One of the most

... Linkage map: order of genetic markers and relative distances from each other - plus how much meiotic recombination (crossing over) there is between homologous chromosomes carrying alternative alleles (genetic markers) ...
A Long-Term Evolutionary Pressure on the Amount of Noncoding DNA
A Long-Term Evolutionary Pressure on the Amount of Noncoding DNA

... proportion of the offspring keep the ancestral phenotype by bearing no mutation or only neutral ones (Van Nimwegen et al. 1999; Wilke 2001a, 2001b; Wilke et al. 2001). Indeed, if the ancestral fitness cannot be retained from one generation to the next because deleterious mutations are too frequent, ...
DNA
DNA

... Minute amounts of DNA template may be used from as little as a single cell. DNA degraded to fragments only a few hundred base pairs in length can serve as effective templates for amplification. Large numbers of copies of specific DNA sequences can be amplified simultaneously with multiplex PCR react ...
Supporting Information for A Convenient Method for Genetic
Supporting Information for A Convenient Method for Genetic

Prof. Kamakaka`s Lecture 15 Notes
Prof. Kamakaka`s Lecture 15 Notes

... Amount of DNA varies between species Amount of DNA varies in eukaryotes Salamander genomes are 20 times larger than human genomes Barley genome is 10 times larger than the rice genome Barley and rice are related. Measurements of DNA length Amount of DNA/nucleus = C value ...
Super models
Super models

... animals (or cells, in the case of yeast) by DNA transformation. These basic tools are essential to dissect and understand gene function. A model organism must also be utilitarian. Practical qualities include a short generation time, small size, and both ease and reasonable cost of maintenance. For ...
Chromatin: a multi-scale jigsaw puzzle
Chromatin: a multi-scale jigsaw puzzle

... Ji-Ping Z. Wang3 & Jonathan Widom2 Eukaryotic genomes are packaged into nucleosome particles that occlude the DNA from interacting with most DNA binding proteins. Nucleosomes have higher affinity for particular DNA sequences, reflecting the ability of the sequence to bend sharply, as required by the ...
Towards identifying the full set of genes involved in post
Towards identifying the full set of genes involved in post

... vital staple food to over 500 million in the humid tropics. Unfortunately, it suffers from a rapid post-harvest physiological deterioration (PPD) that can render the roots uneatable and unmarketable within 24-72 hours of harvest. Increased urbanization has lengthened the distance and time between fa ...
Slide 1
Slide 1

... – If chromosome is lost (one copy = monosomic) = individual does not survive – If chromosome is gained (3 copies = trisomic) = individual may survive but only in a few cases and will be mentally impaired • Example: Trisopy 21 (Down syndrome) ...
Lecture 5
Lecture 5

... Eukaryotic chromosomal organization • Many eukaryotes are diploid (2N) • The amount of DNA that eukaryotes have varies; the amount of DNA is not necessarily related to the complexity (Amoeba proteus has a larger amount of DNA than Homo sapiens) • Eukaryotic chromosomes are integrated with proteins ...
DNA Microarray - School of Biotechnology
DNA Microarray - School of Biotechnology

... • Thus, in this transformation the mapping space is continuous and up-regulation and down-regulation are comparable.  Normalization :-When one compares the expression levels of genes that should not change in the two conditions (say, housekeeping genes), what one quite often finds is that an averag ...
Patalano et al 2015 PNAS - Cambridge Repository
Patalano et al 2015 PNAS - Cambridge Repository

... both species, we found few differences between phenotypes at the transcriptional level, with ...
Treatment of Viruses
Treatment of Viruses

... Origin of Viruses 2. Run-away RNA: Viruses arose from host RNA or DNA that gained a self-replicative, but parasitic existence and acquired the ability to replicate independently of their host ...
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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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