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Magnusiomyces capitatus (de Hoog et al.) de Hoog et Smith
Magnusiomyces capitatus (de Hoog et al.) de Hoog et Smith

... 2.  Concentration by PicoGreen® measurement was found to be approximately 2 µg. 3.  Purity: OD260/OD280 ratio. 4.  Integrity of DNA was determined by electrophoresis on a 1% agarose gel stained with SYBER Safe™, and was found to be of high molecular weight. 5.  No RNA was detected by electrophoresis ...
Solution
Solution

... including  the  Insulin  Growth  Factor  2  gene.  Further  fine  mapping  studies  suggested  the   phenotype  maps  to  a  non-­‐coding  region  nearby  the  IGF2  gene.    This  pig  sequence  is  highly   conserved  in  the  mouse ...
Bacino et al., 2015
Bacino et al., 2015

... can identify mutations in known disease genes, particularly when the phenotype is unusual or atypical compared to previously reported cases. In the case of metabolic disorders, sequencing can reveal underlying defects previously undetected by biochemical studies, such as Argininemia [18] and mitocho ...
Bio499 Bioinformatics
Bio499 Bioinformatics

... other strand. I will assign you a number during the lecture to work on one of the 4 pairs of sequences listed. Please write your assigned number here: _________ 1. Copy your two sequences to Biology Workbench and create a file for each sequence. 2. A typical DNA sequencing reaction can only read as ...
投影片 1
投影片 1

...  Lesch-Nyhan syndrome (LNS) is a rare genetic disorder characterized by an overproduction of uric acid, neurological disability, and behavioral problems. The symptoms of LNS typically appear between ages 3 and 6 months; the presence of orange-colored crystal-like deposits (orange sand) in the child ...
SEGMENTAL VARIATION
SEGMENTAL VARIATION

... • Depth of coverage in a single patient was compared to average and standard deviation of depth of coverage. • Algorithms were developed for: – Classifying X chromosome as being deleted in males compared with females – Classifying X chromosome as being duplicated in females compared with males S L I ...
Topologically Non-linked Circular Duplex DNA
Topologically Non-linked Circular Duplex DNA

... inverted in aqueous methanol solutions. They suggested that this was best explained as an R → L transition, although there are other possible explanations. Similar inversions were demonstrated in the circular dichroism (CD) spectra of DNA at high salt concentration (Zimmer and Luck, 1974), and follo ...
Title A Fluorescently Labeled, Hyperbranched Polymer
Title A Fluorescently Labeled, Hyperbranched Polymer

... of small DNA (18–24 nt) in serum through a change in the fluorescent signal. More specifically, detection is based on the conformational change of the polymer molecules upon binding to the ssDNA probe, producing a measurable fluorescent signal. Hybridization to the target sequence results in a signi ...
Generation of Highly Site-Specific DNA Double
Generation of Highly Site-Specific DNA Double

... from plasmid pI-CreI (21). The I-CreI open reading frame was amplified, cleaved with HhaI and then ligated to the adapter oligonucleotide described above. The resulting nls-Cre fragment was ligated into the NotI site of pCMVb to generate pCNCre3 (Fig. 1A). The I-PpoI homing site plasmid p42 (9) cont ...
Coagulation system during pregnancy
Coagulation system during pregnancy

... stopped at 36 weeks. The action of warfarin is monitored by prothrombin time. S.E. during pregnancy is teratogenicity and bleeding tendency in the fetus, bleeding in the mother. Reversal of the effect is by stopping the drug, it will take three days to reserve the action, so we can give FFP and vita ...
Gene transcription
Gene transcription

Study of Hypertension in Spontaneous Hypertensive Rats by
Study of Hypertension in Spontaneous Hypertensive Rats by

pdf, 1.3 MB - DNA and Natural Algorithms Group
pdf, 1.3 MB - DNA and Natural Algorithms Group

... 3.5. Step 5: dissociation of the motor apparatus The process of replication is complete by this point; we started with two parental superstrands, and we now have two additional daughter superstrands. Just as DNA, replication was semi-conservative; each of the superduplexes contain one parental stran ...
Non-Disjunction & Aneuploidy
Non-Disjunction & Aneuploidy

...  Identifies individuals who might carry a serious genetic disease  Screening of newborns is the first step in preventative medicine  Genetic Counseling ...
Molecular studies on an ancient gene encoding
Molecular studies on an ancient gene encoding

... two, and all three were derived from a common ancestor, the progenote [4]. Whether the progenote was itself a true organism, or represented a prebiotic state of a primitive genetic order, is unresolved. Eukaryotic genes, as well as a small number of prokaryotic and organellar genes, have long interv ...
Document
Document

... In the absence of recBC, strains have trouble growing and suffer broken chromosomes (linear DNA). There is more breakage when rep is missing (which increases replication difficulties), and less breakage when ruvAB is missing. Therefore in strains with replication problems, ruvAB proteins (Holliday j ...
Genomic In Situ Hybridization (GISH) as a Tool to Identify
Genomic In Situ Hybridization (GISH) as a Tool to Identify

... boiling water for 10 min and labeled with digoxingenin-11-dUTP using the nick translation method (Roche Applied Science, Nutley, NJ, USA). Genomic DNA of HA 89 was used as blocking DNA after shearing, with ratios of blocking DNA to probe DNA ranging from 35:1 to 120:1. Different washing stringencies ...
Laboratory manual for the diagnosis of whooping cough caused by... pertussis/ Bordetella parapertussis
Laboratory manual for the diagnosis of whooping cough caused by... pertussis/ Bordetella parapertussis

... responsible for the disease either by culture or by real time polymerase chain reaction (RT-PCR). Indirect diagnosis is essentially by serology and consists of detecting specific antibodies in the serum of an infected individual. Culture is not very sensitive since the percentage of success is gener ...
Single-step generation of rabbits carrying a targeted allele of the
Single-step generation of rabbits carrying a targeted allele of the

... Production of the rabbits carrying the targeted allele of the tyrosinase gene Mature Dutch Belted rabbits were purchased from Kitayama Labes (Nagano, Japan). Fertilized embryos were obtained from mature female rabbits that had been treated with 75 IU of follicle stimulating hormone (Antrin R10; Kyor ...
Chem 465 Biochemistry II Hour Exam 3
Chem 465 Biochemistry II Hour Exam 3

... ones, and what is the tie between Eukaryotic transposons and RNA? A transposon is a piece of DNA that can ‘jump’ from one site to another. In a simple transposon the piece of DNA only contains the sequences required for transposition and the genes for the transposase that does the transposition. In ...
Whole Exome Sequencing
Whole Exome Sequencing

... bulbous nose, short neck, low hairline, growth and mental retardation, parents at risk for balance carrier status 11q deletion: Jacobsen syndrome, ocular hypertelorism, large, mouth, cardiac large carp shaped mouth defects, ParisTrousseau (neonatal thrombocytopenia) ...
Identification of a Novel Streptococcal Gene
Identification of a Novel Streptococcal Gene

... ciprofloxacin-resistant colony from each plate was picked for sequencing analysis to ensure independent mutational events. DNA regions covering bases 228 to 255 and 293 to 314 from the parC gene were analyzed by pyrosequencing of ciprofloxacin-resistant wild-type (wt) and EH58 clones to determine th ...
Genetic causes of male and female infertility
Genetic causes of male and female infertility

... Congenital Absence of Vas Deferens (CAVD) 1-2% male infertility, 6% obstructive azoospermia Mutations (>1300) in CFTR gene (Cystic Fibrosis Transmembrane Conductance Regulator) ...
Maternal uniparental disomyof chromosome 13
Maternal uniparental disomyof chromosome 13

... These investigations are of value firstly for been formed by a translocation involving the determining which chromosomes contain breakpoints p 11.2 in the short arms of identical imprinted genes and secondly for showing the chromosome 13 chromatids before anaphase in chromosomal location of patholog ...
Chapter 2. Structures of Nucleic Acids
Chapter 2. Structures of Nucleic Acids

... were thought to be short oligonucleotides (four or five nucleotides long), functioning primarily in phosphate storage. Thus proteins, with their greater complexity, were the favored candidate for the transforming entity, at least before the experiment was done. Different biochemical fractions of the ...
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Cell-free fetal DNA

Cell-free fetal DNA (cffDNA) is fetal DNA circulating freely in the maternal blood stream. It can be sampled by venipuncture on the mother. Analysis of cffDNA provides a method of non-invasive prenatal diagnosis.cffDNA originates from the trophoblasts making up the placenta. It is estimated that 2-6% of the DNA in the maternal blood is fetal in origin. The fetal DNA is fragmented and makes its way into the maternal bloodstream via shedding of the placental microparticles into the maternal bloodstream (figure 1). Studies have shown that cffDNA can first be observed as early as 7 weeks gestation, and the amount of cffDNA increases as the pregnancy progresses. cffDNA diminishes quickly after the birth of the baby, so that it is no longer detectable in the maternal blood approximately 2 hours after birth. cffDNA is significantly smaller than the maternal DNA in the bloodstream, with fragments approximately 200bp in size. Many protocols to extract the fetal DNA from the maternal plasma use its size to distinguish it from the maternal DNA.Studies have looked at, and some even optimized, protocols for testing non-compatible RhD factors, sex determination for X-linked genetic disorders and testing for single gene disorders. Current studies are now looking at determining aneuploidies in the developing fetus. These protocols can be done earlier than the current prenatal testing methods, and have no risk of spontaneous abortion, unlike current prenatal testing methods. Non-invasive prenatal diagnosis (NIPD) has been implemented in the UK and parts of the US; it has clear benefits above the standard tests of chorionic villi sample (CVS) and amniocentesis which have procedure-related miscarriage risks of about 1 in 100 pregnancies and 1 in 200 pregnancies, respectively.As a method of prenatal diagnosis, cell-free fetal DNA techniques share the same ethical and practical issues, such as the possibility of prenatal sex discernment and sex selection.
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