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DNA Technology Notes
DNA Technology Notes

...  to investigate cellular processes. ...
Laboratory 1: Genetic Mapping In Drosophila
Laboratory 1: Genetic Mapping In Drosophila

... Drosophila is known as a model organism. Model organisms are those whose genetic mechanisms are common to a large group of species, included in these are humans. At first, Drosophila was well used for understanding the mechanisms of how traits are passed from parent to offspring. However, over time ...
Distinct and stage specific nuclear factors regulate the expression of
Distinct and stage specific nuclear factors regulate the expression of

... regulatory regions did not reveal the presence of sequences known to bind general eukaryotic factors. However, we did find parasite specific sequence elements such as poly(dA) poly(dT) tracts, CCAAT boxes and a single 7 bp-G rich sequence, (A/G)NGGGG(C/A) in the 5' upstream regulatory regions of the ...
2010 HSC Exam Paper - Biology
2010 HSC Exam Paper - Biology

... An experiment was conducted to test the effect of dissolved carbon dioxide (CO2) on the pH of water. It was found that the pH of water decreased as CO2 was added. How do these findings relate to the acidity of blood as it circulates in the body? (A) Blood in the veins of muscles becomes less acidic ...
Antifungals - Website of Neelay Gandhi
Antifungals - Website of Neelay Gandhi

... a. Presynaptic inhibition- Release of Ach diminishes and contraction “fades” b. Postsynaptic inhibition- Blocks Ach at receptor. This is a competitive block therefore increased Ach can reverse this. Depolarizing-Competitive agonist that binds to and activates the NMJ receptor but inactivates it by k ...
Asexual Reproduction Slideshow File
Asexual Reproduction Slideshow File

...  Offspring- a new organism produced by one or two parents There are two types of reproduction Asexual Reproduction  Sexual Reproduction ...
No Slide Title
No Slide Title

...  No alcR expression detected in any of the transformed cell lines! ...
DNA RESTRICTION ANALYSIS
DNA RESTRICTION ANALYSIS

... DNA fragments will migrate towards the + anode end. 7. Fill box with TAE buffer, to level that just covers entire surface of gel by about 2mm. 8. Make certain that sample wells left by comb are completely submerged by buffer. 9. The gel is now ready to load with DNA. Loading gel with DNA 1. Your tab ...
DNA Technology Notes (13.1 &13.2)
DNA Technology Notes (13.1 &13.2)

...  to investigate cellular processes. ...
c-fos Protein Can Induce Cellular Transformation: A Novel
c-fos Protein Can Induce Cellular Transformation: A Novel

... show that even though the c-fos protein is completely different from the v-fos protein at its C terminus, it is capable of transforming cultured fibroblasts. However, activation of the transforming potential of the c-fos gene requires two manipulations-a transcriptional enhancer sequence must be lin ...
Rapid and reproducible DNA isolation from 1 ml of whole blood with
Rapid and reproducible DNA isolation from 1 ml of whole blood with

1dl5 Lichtarge lab 2006
1dl5 Lichtarge lab 2006

... One of the table columns is “substitutions” - other amino acid types seen at the same position in the alignment. These amino acid types may be interchangeable at that position in the protein, so if one wants to affect the protein by a point mutation, they should be avoided. For example if the substi ...
Recombinant "Paper" Plasmid Background:
Recombinant "Paper" Plasmid Background:

... for each of the enzymes on the cell DNA. The enzyme must have a m a t c h in two places on the cell DNA: one above the gene and the second below the gene to be useful. Discard any enzyme that cannot cut the cell DNA both above and below the gene. Select one enzyme that can cut the plasmid in one pla ...
Screening for homozygosity by descent in families with autosomal
Screening for homozygosity by descent in families with autosomal

... 1999; Pierce et al. 1999). We have employed the approach of screening for homozygosity by descent since the regions linked to the disease gene are almost certain to be homozygous in affected individuals of a family, and be common to all such members of the same family. The five cases that showed hom ...
Proposal form for the evaluation of a genetic test for NHS Service
Proposal form for the evaluation of a genetic test for NHS Service

... weakness and wasting of the muscles below the knees and often those of the hands. Many affected people also have loss of feeling in the hands and feet. The underlying cause is that the peripheral nerves (which connect the spinal cord to the muscles, joints and skin, carrying messages in both directi ...
Full Article - Pertanika Journal
Full Article - Pertanika Journal

... Banana is one of the important global food commodities. The commercial and subsistence production is seriously threatened by Fusarium wilt caused by soilborne Fusarium oxysporum f. sp. cubense (Foc). Foc race 4 (FocR4) is considered economically important as it causes significant plantation losses i ...
View poster
View poster

... genome sequencing (WGS) or targeted enrichment using exome or gene panels. Copy number variation (CNV) of genomic segments is a large category of structural variation and has been implicated in many Mendelian diseases and complex traits. The impact of CNVs on gene expression is not limited to only t ...
Bez nadpisu - Univerzita Karlova v Praze
Bez nadpisu - Univerzita Karlova v Praze

...  type of C1 INH mutation associated rather with laboratory phenotype than clinical manifestation • missense mutation in the reactive center loop - 75% patients with HAE type II • large deletions, nonsense, frameshift and splicing mutations – causal usually in HAE type I • inframe del/ins, missense ...
An Introduction to Affymetrix Microarrays
An Introduction to Affymetrix Microarrays

... What is a microarray probe? If we know the genetic sequence of the cDNA, we can artificially synthesize a strand of DNA with the same sequence. This is called an oligo(nucleotide). Oligos may be “spotted” on the array like cDNA or may be synthesized on the array ...
View - OhioLINK Electronic Theses and Dissertations Center
View - OhioLINK Electronic Theses and Dissertations Center

... Centrosomes are highly conserved organelles that are composed of two microtubule-based centrioles surrounded by an amorphous protein cloud of pericentriolar material (PCM), which is able to nucleate astral microtubules. They serve as microtubule organizing centers during cell division and are import ...
A novel isoform of human Golgi complex-localized glycoprotein
A novel isoform of human Golgi complex-localized glycoprotein

... GLG1 gene encodes two polypeptides GLG1 and GLG2 A single human GLG1 gene has been identified and localized to chromosome 11q22-q23 (Mourelatos et al., 1995). To determine the molecular basis underlying generation of the two forms of human GLG mRNA, a human genomic phage DNA library was screened wit ...
(From The Rockefdler Institute) Experimental
(From The Rockefdler Institute) Experimental

... presence of 44 aspartic, 27 glutamic acids, and only four basic residues; i.e., one lysine, one histidine, and two arginines. This marked predominance of dicarboxylic acids with 35 free carboxyls8 and the occurrence of one phosphate group (12, 15) explain that pepsin even in 0.1 ~ hydrochloric acid ...
Questions - Vanier College
Questions - Vanier College

... Two prospective parents are meeting with a genetic counsellor because of the presence of factor VIII deficiency hemophilia in both of their families. Factor VIII is a protein that helps the blood to clot, and when a person’s factor VIII level is very low, even the smallest cuts can be troublesome, a ...
The Discovery and Significance of Selected Blood Groups
The Discovery and Significance of Selected Blood Groups

... (GPI) anchor. This was also shown (Telen, et al.) by passing RBCs from patients with PNH through a column coated with anti-DAF and typing the PNHIII RBCs that did not bind to the antibody. ...
AMPK_PhD
AMPK_PhD

... neurogenic weakness ataxia and retinitis pigmentosa. Complex II are rarely affected (Rossignol et al. ...
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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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