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RNA
RNA

... NUCLEOTIDE (Building blocks of Nucleic Acids) ...
Biogenetic Engineering & Manipulating Genes
Biogenetic Engineering & Manipulating Genes

... Manipulating genes and sequencing DNA has become one of the greatest achievements in the last 50 years -First complete genome sequenced was a bacteria (1995) ...
video slide - Wesleyan College Faculty
video slide - Wesleyan College Faculty

... This method synthesizes a nested set of DNA strands complementary to the original DNA fragment. Each strand starts with the same primer and ends with a dideoxyribonucleotide (ddNTP), a modified nucleotide. Incorporation of a ddNTP terminates a growing DNA strand because it lacks a 3—OH group, the s ...
Molecular Biology Primer Part 2 ()
Molecular Biology Primer Part 2 ()

... Electrons and protons are electrically attracted to each other. Almost all of the mass of an atom is in its nucleus; almost all of the volume of an atom is occupied by electrons. The number of protons (also known as its atomic number) determines the element. Varying the number of neutrons results in ...
Key Genes Associated with Cancer Found in Circulating Blood
Key Genes Associated with Cancer Found in Circulating Blood

... genome. The presence of retrotransposons in microvesicles gives them a mechanism for horizontal gene transfer to adjacent cells. The research team also revealed that when tumors have amplification of certain oncogene sequences like c-Myc, this is reflected in the microvesicles isolated from the bloo ...
Chemical synthesis, cloning and expression of human preproinsulin
Chemical synthesis, cloning and expression of human preproinsulin

... sequence contains four substitutions at positions 2-alanine replaced with glycine, 5methionine with isoleucine, 11-leucine with isoleucine and 15-alanine with isoleucine. These changes were introduced to increase restriction sites, such as four Sau3A and two BamHI sites in the codon region which wil ...
Alterations of the PPP2R1B gene located at 11q23 in human
Alterations of the PPP2R1B gene located at 11q23 in human

... analysis and clinicopathological factors. This finding is consistent with the combined findings of two previous studies: tumours with PPP2R1B alterations revealed a high frequency of LOH on chromosome 11q235 and there was no association between LOH on chromosome 11q23 and clinical data (patient sex, ...
Chapter 12 Primary Structure of Nucleic Acids Sequencing Strategies
Chapter 12 Primary Structure of Nucleic Acids Sequencing Strategies

... Cleavage Reactions-Purines • G-specific cleavage by methylation with dimethyl sulfate, followed by treatment with piperidine. (See Figure 12.4 for mechanism) • Purine specific cleavage by treating with acid prior to methylation and piperidine treatment. • Electrophoresis of the two reaction mixtures ...
Sequencing the Human Genome
Sequencing the Human Genome

... The haploid human genome comprises approximately three billion base pairs of DNA that are organized into 23 chromosomes. The order of these nucleotides creates genes, which are discrete units of genetic information that contain the instructions to build and maintain an organism. DNA sequencing is th ...
Basics of Molecular biology
Basics of Molecular biology

... when a single nucleotide — A, T,C, or G — in the genome (or other shared sequence) differs between members of a species or paired chromosomes in an individual. • Used in biomedical research ,crop and livestock breeding programs. ...
Protein Synthesis Lab: Day #1
Protein Synthesis Lab: Day #1

... chromosomes depending on the amount of DNA, or instructions, needed to build and keep that organism functioning. Humans normally have two sets of 23 chromosomes. One set comes from each parent with the same genes, but with different versions of those genes. If they are the same, why do we have two s ...
Transduction
Transduction

... recipient chromosome by breaking both DNA molecules, crossing them over and rejoining them. This process, known as recombination. There are several ...
Present
Present

... Fox Chase Cancer Center Bioinformatics ...
Methods for ARIC Carotid MRI Genotyping Project
Methods for ARIC Carotid MRI Genotyping Project

... TagSNPs that were not in blocks, or only tagged themselves in the YRI population were not included. Nonsynonymous SNPs with a MAF >0.05 and a limited number of additional candidate SNPs were included if provided by an ARIC investigator. The final SNP set for each gene was determined by taking the un ...
Basics of Molecular biology - Server users.dimi.uniud.it
Basics of Molecular biology - Server users.dimi.uniud.it

... when a single nucleotide — A, T,C, or G — in the genome (or other shared sequence) differs between members of a species or paired chromosomes in an individual. •  Used in biomedical research ,crop and livestock breeding programs. ...
Basic Principle in Plant Physiology
Basic Principle in Plant Physiology

... •Excess amino acids are degraded into specific compounds that can be used in other metabolic pathways. •This process begins with the removal of the amino group, which can be converted to urea and excreted. •The a-ketoids that remain are metabolized so that their carbon skeletons can enter glycolysis ...
DNA damage/repair
DNA damage/repair

... Defects in genes encoding proteins involved in mismatch repair, nucleotide-excision repair, and recombinational repair can cause cancer Nucleotide-excision repair sole repair pathway for pyrimidine dimers genetic defect causes XP, xeroderma pigmentosa, these individuals are extremely sensitive to su ...
119KB - NZQA
119KB - NZQA

... parents using gametes. These gametes (sex cells) are formed during meiosis. Gametes have only one set of chromosomes, and so these can be combined with another parent to make a unique individual. This increases variation [OR crossing over OR independent assortment OR meiosis OR fertilisation]. Varia ...
Mechanisms of Glucocorticoid-Regulated Gene Transcription
Mechanisms of Glucocorticoid-Regulated Gene Transcription

... The finding that only the minority of GR binds promoter-proximal is not specific for GR but is also seen for related hormone receptors including ER, PPAR and AR [55, 57, 58]. This suggests that long-range regulation by GR and other hormone receptors might be responsible for the regulation of a large f ...
NCEA Level 1 Science (90948) 2016
NCEA Level 1 Science (90948) 2016

... parents using gametes. These gametes (sex cells) are formed during meiosis. Gametes have only one set of chromosomes, and so these can be combined with another parent to make a unique individual. This increases variation [OR crossing over OR independent assortment OR meiosis OR fertilisation]. Varia ...
Molecular Genetics
Molecular Genetics

...  At the middle of the folded strand, there is a three-base coding sequence called the anticodon.  Each anticodon is complementary to a codon on the mRNA. ...
Controlling Gene Expression in Bacteria
Controlling Gene Expression in Bacteria

... cells all the time. These continually expressed genes are called constitutive genes.  Other genes are only needed by certain cells or at specific times. The expression of these inducible genes is tightly controlled.  For example, pancreas beta cells make the protein insulin by expressing the insul ...
PART I
PART I

... In every case, the recombinant DNA must be taken up by the cell in a form in which it can be replicated and expressed. This is achieved by incorporating the DNA in a vector. A number of viruses (both bacterial and of mammalian cells) can serve as vectors. But here let us examine an example of clonin ...
Transcription 12.06.21 lec
Transcription 12.06.21 lec

... Transcription.  Here's  a  strand  of  DNA  that  gets  split  apart;  then  there's  the  initial  copying  of  that  chain.  Transcription  is  where   you're  just  making  pieces  of  RNA  from  DNA.  Translation's  where  you  act ...
The nucleosome
The nucleosome

... H3-K4 methylation is generally associated with trx active chromatin.  di-methyl H3-K4 appears to be a global epigenetic mark in euchromatic regions and tri-methylation of H3-K4 correlates with active transcription  both H3-K4 and H3-K79 participate in establishing euchromatic regions by preventing ...
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Promoter (genetics)



In genetics, a promoter is a region of DNA that initiates transcription of a particular gene. Promoters are located near the transcription start sites of genes, on the same strand and upstream on the DNA (towards the 5' region of the sense strand).Promoters can be about 100–1000 base pairs long.
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