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Friday, February 2, 2018

What's is AIDS



AIDS stands for Acquired Immune Deficiency Syndrome:
·          Acquired means you can get infected with it.
·          Immune Deficiency means a weakness in the body’s system that fights diseases.
·          Syndrome means a group of health problems that make up a disease.

AIDS is caused by a virus called HIV, the Human Immunodeficiency Virus. If you get infected with HIV, your body will try to fight the infection. It will make “antibodies,” special molecules to fight HIV.

A blood test for HIV looks for these antibodies. If you have them in your blood, it means that you have HIV infection. People who have the HIV antibodies are called “HIV-Positive.” Fact Sheet 102 has more information on HIV testing.

Being HIV-positive, or having HIV disease, is not the same as having AIDS. Many people are HIV-positive but don’t get sick for many years. As HIV disease continues, it slowly wears down the immune system. Viruses, parasites, fungi, and bacteria that usually don’t cause any problems can make you very sick if your immune system is damaged. These are called “opportunistic infections.” See Fact Sheet 500 for an overview of opportunistic infections.




HOW DO YOU GET AIDS?
You don’t actually “get” AIDS. You might get infected with HIV, and later you might develop AIDS. You can get infected with HIV from anyone who’s infected, even if they don’t look sick and even if they haven’t tested HIV-positive yet. The blood, vaginal fluid, semen, and breast milk of people infected with HIV has enough of the virus in it to infect other people. Most people get the HIV virus by:
·          having sex with an infected person
·          sharing a needle (shooting drugs) with someone who’s infected
·          being born when their mother is infected, or drinking the breast milk of an infected woman

Getting a transfusion of infected blood used to be a way people got AIDS, but now the blood supply is screened very carefully and the risk is extremely low.

There are no documented cases of HIV being transmitted by tears or saliva, but it is possible to be infected with HIV through oral sex or in rare cases through deep kissing, especially if you have open sores in your mouth or bleeding gums. For more information, see the following Fact Sheets:
·          150: Stopping the Spread of HIV
·          151: Safer Sex Guidelines
·          152: How Risky Is It?

The Centers for Disease Control and Prevention (CDC) estimates that 1 to 1.2 million US residents are living with HIV infection or AIDS; about a quarter of them do not know they have it. About 75 percent of the 40,000 new infections each year are in men, and about 25 percent in women. About half of the new infections are in Blacks, even though they make up only 12 percent of the US population. In the mid-1990s, AIDS was a leading cause of death. However, newer treatments have cut the AIDS death rate significantly. For more information, see the US Government fact sheet at http://www.niaid.nih.gov/factsheets/aidsstat.htm




WHAT HAPPENS IF I’M HIV POSITIVE?
You might not know if you get infected by HIV. Within a few weeks after being infected, some people get fever, headache, sore muscles and joints, stomach ache, swollen lymph glands, or a skin rash for one or two weeks. Most people think it’s the flu. Some people have no symptoms. Fact Sheet 103 has more information on the early stage of HIV infection.

The virus will multiply in your body for a few weeks or even months before your immune system responds. During this time, you won’t test positive for HIV, but you can infect other people.

When your immune system responds, it starts to make antibodies. When this happens, you will test positive for HIV. After the first flu-like symptoms, some people with HIV stay healthy for ten years or longer. But during this time, HIV is damaging your immune system.

One way to measure the damage to your immune system is to count your CD4 cells. These cells, also called “T-helper" cells, are an important part of the immune system. Healthy people have between 500 and 1,500 CD4 cells in a milliliter of blood. Fact Sheet 124 has more information on CD4 cells.

Without treatment, your CD4 cell count will most likely go down. You might start having signs of HIV disease like fevers, night sweats, diarrhea, or swollen lymph nodes. If you have HIV disease, these problems will last more than a few days, and probably continue for several weeks.

HOW DO I KNOW IF I HAVE AIDS?
HIV disease becomes AIDS when your immune system is seriously damaged. If you have less than 200 CD4 cells or if your CD4 percentage is less than 14%, you have AIDS. See Fact Sheet 124 for more information on CD4 cells. If you get an opportunistic infection, you have AIDS. There is an “official” list of opportunistic infections, put out by the Centers for Disease Control (CDC). The most common ones are:
·          PCP (Pneumocystis pneumonia), a lung infection; see Fact Sheet 515
·          KS (Kaposi’s sarcoma), a skin cancer, Fact Sheet 511
·          CMV (Cytomegalovirus), an infection that usually affects the eyes, Fact Sheet 504
·          Candida, a fungal infection that can cause thrush (a white film in your mouth) or infections in your throat or vagina, Fact Sheet 501

AIDS-related symptoms also include serious weight loss, brain tumors, and other health problems. Without treatment, these opportunistic infections can kill you. The official (technical) CDC definition of AIDS is available at http://www.cdc.gov/mmwr/preview/mmwrhtml/00018871.htm

AIDS is different in every infected person. A few people may die a few months after getting infected, but most live fairly normal lives for many years, even after they “officially” have AIDS. A few HIV-positive people stay healthy for many years even without taking antiretroviral medications (ART).




IS THERE A CURE FOR AIDS?
There is no cure for AIDS. Antiretroviral therapy (ART, see fact sheet 403) can slow down the HIV virus and slow down the damage to your immune system. Most people stay healthy as long as they continue ART. There is no way to “clear” HIV from the body.

Other drugs can prevent or treat opportunistic infections (OIs). In most cases, these drugs work very well. The newer, stronger ARVs have also helped reduce the rates of most OIs. A few OIs, however, are still very difficult to treat. See Fact Sheet 500 for more information on opportunistic infections.




Inout Scripts™ : Based in Kerala India Fake Scripts Sacmming You and Me

They use popular social networks to post a huge of fake blogs. They spent a lot in advertising to induce amateur customers to purchase their so called "clone scripts". They scammed much money by providing "customization".

Worst Scripts EVER. InOut Scripts is a scaming company also ther head company Nesote. Spend over $1400 for not working scripts.

Please be warned. don‘t buy a script off this company

Low Trust Rating. This Site May Not Be Safe to Use.

This site is using an anonymous service - which prevents us from identifying the site owner. This can sometimes be just so that the owner does not receive spam, but be aware that many scam sites use this as a method to hide their identify. If this is an ecommerce site - we would suggest you confirm the business address with the website owners.This website has been listed on a threat site at sometime in it's life. These can relate to virus/malware issues

How did inoutscripts.com get a Trust Score of 10% ?

When checking inoutscripts.com we looked at many factors, such as the ownership details, location, popularity and other sites relating to reviews, threats, phishing etc. Although a site like may have a high trust rating, it's worth just checking the countries involved as these could indicate that goods would be shipped from abroad rather than your home country.

The internet is populated with many fake and scam sites - with many being created daily purely to look genuine. Even many review sites are tainted with fake reviews making it almost impossible for somedbody to detect a safe site from a scam. We attempt to analyse the website information and provide a trust guide that will help you determine the risk rating of the inoutscripts.com website.

Is inoutscripts.com a fake site ? Is inoutscripts.com legit and trustworthy ?


Do not purchase anything from InOutScripts.com. I bought their ad software and spent $900 dollars on it and bought 4 of the optional modules that include the CPC, CPI, CPM and CPA modules and they all have issues. It doesn't work properly. If you're thinking of ad server software then steer clear of this company. I lost my money and could not get it back. They do not offer refunds.


Thursday, February 1, 2018

What's wrong with Inout scripts?

15 months ago, I searched online and was attracted by advertisement by Inoutscripts.com. I purchased their Inout Socialtiles v2.0 and its addons for $447 totally.
I found there were no functions of Recap. and email confirmation. The site had been spammed and hacked frequently. I contacted with the tech support, named Nair, and she told me that I had to pay for another $800 costomization fee to add these 2 features.
The speed of this script was very slow.  Sometimes, you logged in but could not logged out. The background picture was unchangeable. The “file share” addon was not working.
They neither refund, nor fixed the script. Actually, they had no professional developers to do the troubleshooting and customization. They are a team of scammers.
Finally, I had to give up the software, and changed into Oxwall.
Believe me. You should not do any business with this criminal company. They are a group of cheaters located in KeralaIndia. Their main members are Jacob, Kumar, Nair, and Saranya. Their address is located at: 1st Fl, Phase IV Carnival Infopark, Kochi, Kerala 682042,India.
They have other phishing sites:
Phishing site 1.  http://www.inoutscripts.com
Phishing site 2.  http://www.enterspine.com/
Phishing site 3.  https://www.parishcloud.com/
Phishing site 4. https://www.parishcloud.com/
Phishing site 5. https://www.storecave.com/
Phishing site 6. https://www.nesote.com/
If you are the victim of Inoutscripts, please contact me freely. Let’s bring these bad guys to justice together.
Inout Socialtiles v2.0                  :447
Inout Socialtiles v2.0                     $249
Mobile addon                                 $99
File share                                         $99

Wednesday, January 31, 2018

What happened to Inoutscripts Socialtiles?

15 months ago, I searched online and was attracted by advertisement by Inoutscripts.com. I purchased their Inout Socialtiles v2.0 and its addons for $447 totally.
I found there were no functions of Recap. and email confirmation. The site had been spammed and hacked frequently. I contacted with the tech support, named Nair, and she told me that I had to pay for another $800 costomization fee to add these 2 features.
The speed of this script was very slow.  Sometimes, you logged in but could not logged out. The background picture was unchangeable. The “file share” addon was not working.
They neither refund, nor fixed the script. Actually, they had no professional developers to do the troubleshooting and customization. They are a team of scammers.
Finally, I had to give up the software, and changed into Oxwall.
Believe me. You should not do any business with this criminal company. They are a group of cheaters located in Kerala India. Their main members are Jacob, Kumar, Nair, and Saranya. Their address is located at: 1st Fl, Phase IV Carnival Infopark, Kochi, Kerala 682042, India.
They have other phishing sites:
Phishing site 1.  http://www.inoutscripts.com
Phishing site 2.  http://www.enterspine.com/
Phishing site 3.  https://www.parishcloud.com/
Phishing site 4. https://www.parishcloud.com/
Phishing site 5. https://www.storecave.com/
Phishing site 6. https://www.nesote.com/
If you are the victim of Inoutscripts, please contact me freely. Let’s bring these bad guys to justice together.
Inout Socialtiles v2.0                  :447
Inout Socialtiles v2.0                     $249
Mobile addon                                 $99
File share                                         $99


Saturday, January 27, 2018

Gel Filtration Chromatography

Gel Filtration Chromatography Applications
Gel filtration chromatography, a type of size exclusion chromatography, can be used to either fractionate molecules and complexes in a sample into fractions with a particular size range, to remove all molecules larger than a particular size from the sample, or a combination of both operations. Gel filtration chromatography can be used to separate compounds such as small molecules, proteins, protein complexes, polysaccharides, and nucleic acids when in aqueous solution. When an organic solvent is used as the mobile phase, the process is instead referred to as gel permeation chromatography.
Gel filtration chromatography can also be used for:
1.      Fractionation of molecules and complexes within a predetermined size range
2.      Size analysis and determination
3.      Removal of large proteins and complexes
4.      Buffer exchange
5.      Desalting
6.      Removal of small molecules such as nucleotides, primers, dyes, and contaminants
7.      Assessment of sample purity
8.      Separation of bound from unbound radioisotopes
Gel filtration chromatography media for all of the above uses are available in prepacked gravity flow columns, spin columns, low-pressure and medium-pressure chromatography columns, and bottled resins.
Gel Filtration Chromatography Mechanism
In a gel filtration chromatography column, the stationary phase is composed of a porous matrix, and the mobile phase is the buffer that flows in between the matrix beads. The beads have a defined pore size range, known as the fractionation range. Molecules and complexes that are too large to enter the pores stay in the mobile phase and move through the column with the flow of the buffer. Smaller molecules and complexes that are able to move into the pores enter the stationary phase and move through the gel filtration column by a longer path through pores of the beads.
Any molecule or complex that is above the fractionation range for a particular gel filtration chromatography column will move through the column faster than any molecule that can enter the stationary phase. Therefore, any constituent in the sample that is above the fractionation range will elute first (in the void volume) before anything that is in the fractionation range. The minimum size that will remain in the mobile phase and not enter the stationary phase is known as the exclusion limit. Bio-Rad offers gel filtration chromatography media and columns with exclusion limits ranging over three orders of magnitude, from 100 daltons to 100,000 daltons (100 kDa).
Molecules and complexes that can enter the stationary phase will be fractionated according to their sizes. Smaller molecules will migrate deep into the pores and will be retarded more than larger molecules that do not so easily enter the pores, and are thus eluted from the column more quickly. This difference in pore migration leads to fractionation of components by size with the largest eluting first.
In gel filtration chromatography columns designed for desalting, buffer exchange, and the removal of small molecules such as nucleotides, the salts and small compounds readily enter the pores, are retarded, and migrate more slowly through the column than the larger proteins or nucleic acids. Therefore, the components of interest in the sample are eluted in advance of salts, nucleotides, etc. DNA cleanup kits using this mechanism often contain gel filtration spin columns.
Resolution, here defined as the sharpness of the boundaries between size fractions, is determined by bead size and a number of other factors. Smaller bead size generally yields higher resolution in a gel filtration chromatography column. Compact molecules diffuse through the stationary phase faster than linear molecules. Size exclusion, fractionation range, and elution rate are affected by buffer composition, ionic strength, and pH. For the fractionation of complex mixtures of proteins, elution times and size exclusion limits may need to be determined empirically.
Gel Filtration Chromatography Media
An important criterion for gel filtration chromatography media is that media is inert and that nothing in the sample or any buffer binds to the media. Another consideration is the type of gel filtration column being used and whether it is used in a pressurized chromatography system or gravity flow or spin columns. If a pressurized chromatography system is being used, both the column and the media must be able to tolerate the pressure and flow rates used.
Commonly used media for gel filtration chromatography are based on agarose or polyacrylamide beads, dextrose for gravity or low-pressure systems, and polymeric resins for medium-pressure systems. The choice of media depends on the properties of the components to be separated and other experimental factors. The following are general considerations when determining the choice of gel filtration chromatography media:
l       Fractionation range
l       Size exclusion limit
l       Operating pressure
l       Flow rate
l       Sample viscosity
l       pH range
l       Autoclavability
Tolerance for water-miscible organic solvents; some samples may be more soluble in a water-organic mix
Tolerance for detergents, chaotropic agents, formamide, etc.
Operating temperature
The types of samples, choice of media, and the chromatography system setup will determine which parameters are the most important for a given purification application.


Gel Filtration �C A Handbook for Gel Filtration Chromatography
this symbol highlights troubleshooting advice to help analyse and resolve .... or for other chromatography techniques and assays. Gel filtration in group ...
kirschner.med.harvard.edu/files/protocols/GE_gelfiltration.pdf

Gel filtration chromatography seprarates proteins, prptides, and oligonucleotides on the basis of size. Molecules move through a bed of porous beads, ...
www.sigmaaldrich.com/.../Protein_Analysis/Chromatography/Gel_Filtration_Chromatography.html

Gel filtration chromotography is based off of the principal of gravity. Most simply, it is a large, vertical tube. Inside this tube, many tiny beads of ...
student.biology.arizona.edu/honors2003/group04/gelfiltration.html

Gel filtration chromatography separates substances on the basis of their size. ... For gel filtration chromatography, it is important to apply the sample to ...
www.science.smith.edu/departments/Biochem/Biochem_353/cytoprep.html

Gel filtration chromatography or perhaps just gel filtration is used to separate or purify protein based on the size properties. ...
envirodiary.com/2007/05/18/gel-filtration-chromatography-procedures

Gel filtration chromatography ge healthcare life sciences
The principle of Gel Filtration Chromatography Separation in Gel Filtration Chromatography is based on the differences in sizes from biomolecules as they ...
www5.gelifesciences.com/.../Content/44B2ACD2F1401137C12572FA00812CF3/

Students use gel-filtration chromatography to separate three proteins whose molecular weights differ significantly and whose activities are simple to ...
faculty.mansfield.edu/bganong/biochemistry/gfc3.htm

GEL FILTRATION CHROMATOGRAPHY (9/16/03 and 9/23/03). Packing the column. ***Note: Do not let the column run dry. Always have buffer above the level of the ...
www.shsu.edu/~chm_mfp/gel_filtration_chromatography.htm

analytical gel filtration chromatography. A preliminary abstract .... gel filtration chromatography of S100B(PP) in the absence of CaZ+ (10 pM subunit ...
www.proteinscience.org/cgi/reprint/6/7/1577.pdf

Nature Protocols is an interactive online resource for all laboratory ... and characterization of transcribed RNAs using gel filtration chromatography ...
www.nature.com/nprot/journal/v2/n12/abs/nprot.2007.480.html

General Protocol 1. Prepare Column for gel filtration chromatography, and ...
Gel Filtration Chromatography. ? separates solutes based on molecular size. ? also called molecular sieve chromatography or size. exclusion chromatography ...
www.tulane.edu/~wiser/methods/handouts/class/09_chrom.pdf

Gel filtration chromatography. Gel filtration chromatography was used to separate soluble proteins fromvesicle-associated proteins based on the time required for ...
https://www.sciencedirect.com/.../gel-filtration-chromatography



How about www.inoutscripts.com celebrities script?

I purchased the Inout Celebrities Script one year ago, but found script was not updated properly. It is still using PHP 5.4 engine. The site is very slow. What is nore that the script is not responsive designed. If you ask them for the mobile edition, they will charge you another $800 as a customization. Finally, I gave up the site.
 There are totally 14 bugs and 25 warnings with this Inout Script.

The manager Kumar and its boss Jacob are cheaters. Finally, they will take the cash and leave you nothing working. Their support email address, suppoet@inoutscripts.com has been world widely labeled as phishing scam.

They advertise with overstated words to induce customers to purchase their so called "clone scripts". We purchased 13 of them, and just found they were full of errors and bugs. Their main group members are Jacob, Kumar, Nair, and Saranya. All of them locate at a small room in Karala, India.

If you are the victim of Inoutscripts, don't hesitate to contact me.
They have other phishing sites:
Phishing site 1.  http://www.inoutscripts.com
Phishing site 2.  http://www.enterspine.com/
Phishing site 3.  https://www.parishcloud.com/
Phishing site 4. https://www.parishcloud.com/
Phishing site 5. https://www.storecave.com/
Phishing site 6. https://www.nesote.com/

Believe me. Don’t purchase any scripts from Inoutscripts.com. They are liars, cheaters, and scamming.

Inoutscripts.com the infamous India scamming company

Gene therapy

Gene therapy involves supplying a functional gene to cells lacking that function, with the aim of correcting a genetic disorder or acquired disease. Gene therapy can be broadly divided into two categories. The first is alteration of germ cells, that is, sperm or eggs, which results in a permanent genetic change for the whole organism and subsequent generations. This “germ line gene therapy” is considered by many to be unethical in human beings. The second type of gene therapy, “somatic cell gene therapy”, is analogous to an organ transplant. In this case, one or more specific tissues are targeted by direct treatment or by removal of the tissue, addition of the therapeutic gene or genes in the laboratory, and return of the treated cells to the patient. Clinical trials of somatic cell gene therapy began in the late 1990s, mostly for the treatment of cancers and blood, liver, and lung disorders.

Despite a great deal of publicity and promises, the history of human gene therapy has been characterized by relatively limited success. The effect of introducing a gene into cells often promotes only partial and/or transient relief from the symptoms of the disease being treated. Some gene therapy trial patients have suffered adverse consequences of the treatment itself, including deaths. In some cases, the adverse effects result from disruption of essential genes within the patient's genome by insertional inactivation. In others, viral vectors used for gene therapy have been contaminated with infectious virus. Nevertheless, gene therapy is still held to be a promising future area of medicine, and is an area where there is a significant level of research and development activity.


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