Thursday, November 12, 2009

Colgate Soothe N Seal

Male infertility is likely to double, alarm from Milan

For experienced emergency genital diseases of the future: a guide for families of the San Paolo

LONDON-A bomb. For specialists in Milan genital diseases and male sex are an underwater world that threatens to double the incidence of infertility among young people. Boys, abolished the visit of the lever, get the diagnosis of these diseases when it is too late. Result: boom and infertile carriers of sexually transmitted diseases that might infect the partner. The warning is the endocrine-andrologist Mario Mancini, head of the surgery of pediatric hospital Andrology San Paolo in Milan. The expert talks to the data in hand: "From our surveys in high schools in the city shows that a second adolescent does not use a condom. 25% of these came into contact with infections and 12.5% \u200b\u200bturns into "infector". But the situation is no different even in the rest of Italy. "

INFECTIONS AND MORE - There is a universe of andrological diseases that comes out: varicocele and testicular problems, sexually transmitted diseases, tumors. "We could be facing the real emergence of the future. Other than influenza, "warns Mancini. Diseases which, if not diagnosed in time, lead to infertility, "We realized that a young infertile three shows signs of damage from chronic prostate infection. Which makes us think that their infertility was preventable. "

the booklet - The experts of St. Paul are so worried that, in collaboration with the Council of Zone 6 (the area in Milan where the hospital is located), have decided to launch a handbook: "The world under the ' navel-Andrology of the boy, "and distribute it in the study of general practitioners and pediatricians. A dozen pages in which, with simple and direct language, the specialists offer adolescents and their families with information useful to detect possible problems. Objective: To support prevention and early detection. The booklet is particularly aimed at providing adolescents and their families all the information needed to understand se per un particolare problema andrologico c'è bisogno di chiedere l'aiuto del medico di famiglia, del pediatra o dello specialista, oppure se rientra in una situazione di normalità.

Origine:corriere.it
Test Infertilità Maschile

Tuesday, November 10, 2009

What Can I Give 5month Old For Cough

Generation of DNA profiles from fabrics without DNA extraction

Abstract...

DNA profiles can be obtained from fabrics where a person has made direct contact with clothing. A standard approach is to cut out a section of the fabric and then use a commercially available method to extract and isolate the DNA. Alternative methods to isolate DNA include the use of adhesive tape to remove traces of cellular material from the fabric prior to extraction. We report on a process to obtain full DNA profiles using direct amplification from a range of fabrics. The absence of an extraction step both reduces the opportunity for contamination and reduces the loss of DNA during the extraction process, increasing the sensitivity of the process of generating a DNA profile. The process does not require the use of commercially available extraction kits thus reducing the cost of generating a DNA profile from trace amounts of starting material. The results are in part dependent upon the nature of the fabric used to which the DNA has been transferred.

Origine:fsigenetics.com

Megalodon Still Exist D

Casework testing of the multiplex kits AmpF ℓ STR ® SEfiler Plus ™ PCR amplification kit (AB), PowerPlex ® S5 System (Promega) and AmpF ℓ STR ® MiniFiler ™ PCR

Abstract

The STR kits SEfiler Plus™ (D3S1358, FGA, D8S1179, D18S51, D21S11, TH01, VWA, SE33, D2S1338, D16S539, D19S433, and Amelogenin), PowerPlex® S5 System (D18S51, D8S1179, TH01, FGA, Amelogenin) and MiniFiler™ (D13S317, D7S820, Amelogenin, D2S1338, D21S11, D16S539, D18S51, CSF1PO, and FGA) were comparatively tested for their robustness and sensitivity. About fifty stains with highly degraded DNA and little DNA quantity served as examination material (e.g. hair with a telogen root, bones, degraded saliva stains on drinking-vessels and skin cell mixtures).

The PowerPlex® S5 with five German-DNA-database (DAD)-systems and the MiniFiler kit with four topical DAD-systems and further STR markers show reduced amplicon lengths. The SEfiler Plus™ kit represents no MiniSTR multiplex, but contains the nine current DAD-systems and further three systems D2S1338, D16S539, D19S433, which are the potential expansion markers for the German-DNA-database.

We have detected on the basis of our comparative stain investigations, that the SEfiler Plus kit was less sensitive than the PowerPlex® S5 and the MiniFiler kit. The MiniFiler™ and the PowerPlex® S5 kit showed a comparative high sensitivity.

Especially in analysing skin cell mixtures, the MiniFiler kit contained larger differences with regard to the performance of the fluorescent dyes/primer concentration co-ordination than the PowerPlex® S5. The SEfiler Plus kit generated – just as both MiniSTR kits – relative robust typing results, but there appeared an increased sensitivity for “allelic drop-outs” and “imbalances”. Since the SEfiler Plus kit was not planned as MiniSTR concept, “allelic drop-outs” were observed, as expected, more frequent in typing stains with degraded DNA and little DNA quantity, especially in the long PCR products (e.g. D18S51).

Origine: fsigenetics.com

Amature Surgeon Xmas App

Developmental validation of the PowerPlex ® 16 System HS: An improved 16-locus fluorescent STR multiplex

Abstract....

STR multiplexes remain the cornerstone of genotyping forensic samples. The PowerPlex® 16 HS System contains the core CODIS loci: D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D21S11, CSF1PO, FGA, TH01, TPOX, and vWA. Additional loci amplified in the multiplex reaction are the sex-determinant locus, amelogenin, and two pentanucleotide STR loci, Penta D and Penta E. The PowerPlex® 16 HS System is an updated version of the PowerPlex 16® System; while the primers and dyes remain unchanged, it introduces an enhanced buffer system that includes hot-start Taq DNA polymerase and ensures robust performance. Due to the modification of the reaction mix, a multi-laboratory developmental validation study was completed to document performance capabilities and limitations for the revised assay. Data within this validation was generated by eight laboratories and served as the basis for the following conclusions: genotyping of single-source samples was consistent across a large range of template DNA concentrations with most laboratories obtaining complete profiles at 62.5pg. Mixture analyses showed that over 90% of minor alleles were detected at 1:9 ratios. Optimum amplification cycle number was ultimately dependent on the sensitivity of the detection instrument and could be adjusted to accommodate a range of DNA template concentrations. Reaction conditions including volume and annealing temperature as well as the concentrations of primers, Taq DNA polymerase, and magnesium were shown to be optimal and able to withstand moderate variations without affecting multiplexed STR amplification. Finally, data from non-probative samples and concordance studies showed consistent results when comparing the PowerPlex® 16 HS System with the PowerPlex® 16 System as well as other commercially available systems.

Origine:fsigenetics.com