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gen-305-presentation-8-16
gen-305-presentation-8-16

... that an organism possesses – In bacteria, it is typically a single circular chromosome – In eukaryotes, it refers to one complete set of nuclear chromosomes – Note: • Eukaryotes possess a mitochondrial genome • Plants also have a chloroplast genome Copyright ©The McGraw-Hill Companies, Inc. Permissi ...
CHAPTER 19 DNA Mutation and Repair
CHAPTER 19 DNA Mutation and Repair

... 1. Chemical mutagens may be naturally occurring, or synthetic. They form different groups based on their mechanism of action: a. Base analogs depend upon replication, which incorpocates a base with alternate states (tautomers) that allow it to base pair in alternate ways, depending on its state. i. ...
Transcription
Transcription

PDS 803482 Ron Blood and Cell DNA Mini
PDS 803482 Ron Blood and Cell DNA Mini

... contains spin columns, buffers and reagents necessary for cell lysis, DNA binding, washing and elution of DNA into small volume. Each kit contains a manual with detailed protocols of DNA extraction and purification from whole blood and cell culture. Ron’s Blood and Cell DNA Mini Kit offers a timesav ...
Preliminary  Characterization  of BYN4, Rhodobacter sphaeroides Alcohol Metabolism
Preliminary Characterization of BYN4, Rhodobacter sphaeroides Alcohol Metabolism

... or nitrous oxide (4). R. sphaeroidesis also able to utilize some alcohols as carbon and energy sources. To metabolize alcohols, bacteria use internal enzymes known as alcohol dehydrogenases (ADHs) to break down the alcohol into compounds that can be readily incorporated into cellular material. From ...
Protocol for RiboShredder™ RNase Blend
Protocol for RiboShredder™ RNase Blend

... RiboShredder™ RNase Blend is a proprietary blend of potent RNases that completely degrade unwanted RNA in DNA purification procedures. Unlike other RNase cocktails, RiboShredder RNase Blend completely degrades all RNA. RiboShredder RNase Blend uses recombinant, highly purified ribonucleases and thus ...
Perl Laboratory Study Guide – Section I
Perl Laboratory Study Guide – Section I

... Add a line that takes an output filename from the command line. For example, the command line should be something like: perl ex6-1.pl infile.fasta outfile.txt At the end of the script, add a couple of lines that open, and write to, a results file. Below is an example of what writing to a file might ...
DNA, Technology, and Florida Strawberries 1 - EDIS
DNA, Technology, and Florida Strawberries 1 - EDIS

... certain DNA sequences present at thousands of points along the chromosomes of cultivated strawberry. These DNA sequences can be thought of as the physical addresses of specific chromosome locations, and some will be close by or even inside certain genes of interest. Today, powerful technologies allo ...
Pdf - Text of NPTEL IIT Video Lectures
Pdf - Text of NPTEL IIT Video Lectures

... where two parental D N A strands separate to allow the replication. Helicase this is enzyme, which helps in unwinding a polynucleotide double helix using the energy, which is derived from a t p hydrolysis primase. This enzyme catalyses synthesis of small pieces of R N A, which is complementary to wh ...
Rapid sequencing of DNA based on single molecule detection
Rapid sequencing of DNA based on single molecule detection

Protein expression, purification, and molecular cloning
Protein expression, purification, and molecular cloning

Plasmids - canesbio
Plasmids - canesbio

... multiple copies of a gene. Foreign DNA is inserted into a plasmid, and the recombinant plasmid is inserted into a bacterial cell. Reproduction in the bacterial cell results in cloning of the plasmid including the foreign DNA. This results in the production of multiple copies of a single gene. ...
Jordan University of Science and Technology Abstract: Authors
Jordan University of Science and Technology Abstract: Authors

LiMA overview
LiMA overview

... detection of bacterial genomes by PCR • LiMA is generic – all bacteria tested contain NAD-dependent DNA ligase. It is difficult to ensure that direct PCR is generic. • LiMA is more sensitive than direct PCR. LiMA involves lysis of the bacilli and release of many ligase molecules which amplify the ta ...
Brooker Chapter 16
Brooker Chapter 16

... This suggests that TNRE can occur more frequently during oogenesis or spermatogenesis, depending on the gene involved. Copyright ©The McGraw-Hill Companies, Inc. Permission required for reproduction or display ...
Bacterial Transformation Lab: Analyzing Results – Answer questions
Bacterial Transformation Lab: Analyzing Results – Answer questions

Frequently Asked Questions - University of South Alabama
Frequently Asked Questions - University of South Alabama

... 4. All biohazardous agents and rDNA registrations are reviewed by the IBC. The IBC typically meets on a quarterly or as-needed basis. In the event a new registration is submitted for review shortly after a convened meeting, the application may be distributed to all committee members for review and v ...


... schiff bases are particularly focused because of their sensitivity towards molecular environment. Transition metal complexes with schiff bases are studied extensively in the past few years, as they have been found to play an important role in the biological applications1.. It binds to different meta ...
Genes, Genomics, and Chromosomes
Genes, Genomics, and Chromosomes

... hybridization of mRNAs to their cDNAs The example given below is to compare the mRNA population differences of RNA isolated from estrogen treated trout liver to its untreated control:  Isolate total RNA samples from livers of estrogen treated fish and control (RNAind & RNAunind)  Prepare 32P-label ...
DNA methylation
DNA methylation

... Polycomb group PRC2 complex containing Jarid2 shown in red), at promoters. Additionally, bivalent genes have non-methylated CpG DNA regions (non-mCpG), and possess repressive H2AK119Ub1 marks (deposited by Ring1a/b ubiquitin E3 ligases within a PRC1 complex shown in dark blue), at the promoter regio ...
2 Marks
2 Marks

... What is transduction? Who discovered it and in which organism? ...
New Developments in Quantitative Real
New Developments in Quantitative Real

... under isothermal conditions, i.e. at a fixed, user-defined temperature (reviewed by Gill and Ghaemi, 2008). The helicase-dependent (HDA) amplification system is one such novel ‘non-PCR’ system for amplifying target DNA (Vincent et al., 2004) and RNA (Goldmeyer et al., 2007), under isothermal conditi ...
Biol115 The Thread of Life
Biol115 The Thread of Life

... • Promoters signal the initiation of RNA synthesis • Transcription factors mediate the binding of RNA polymerase and the initiation of transcription • The completed assembly of transcription factors and RNA polymerase II bound to a promoter is called a transcription initiation complex • A promoter c ...
Policy for sample drop-off and storage in the DNA Analysis Facility
Policy for sample drop-off and storage in the DNA Analysis Facility

... Primers and Probe-Primers sets should be placed in the Investigators Box in the “TaqMan Freezer” located in 305 HSRF. cDNA samples should be in a box (not an open rack) and clearly labeled with the user’s name, the Investigator’s name and the date. These should be placed on the shelf in front of or ...
Restriction fragment length polymorphism in the exon 2 of the BoLA
Restriction fragment length polymorphism in the exon 2 of the BoLA

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Replisome



The replisome is a complex molecular machine that carries out replication of DNA. The replisome first unwinds double stranded DNA into two single strands. For each of the resulting single strands, a new complementary sequence of DNA is synthesized. The net result is formation of two new double stranded DNA sequences that are exact copies of the original double stranded DNA sequence.In terms of structure, the replisome is composed of two replicative polymerase complexes, one of which synthesizes the leading strand, while the other synthesizes the lagging strand. The replisome is composed of a number of proteins including helicase, RFC, PCNA, gyrase/topoisomerase, SSB/RPA, primase, DNA polymerase I, RNAse H, and ligase.
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