NationStates Jolt Archive

Rules:
Do your own math. If your math is incorrect, we will add a surcharge of one percent (1%) to the correct total.

All prices are in US Dollars. We will check, using public records thirdgeek - the Public Health and/or Defence or Law & Order sections - if a nation, a link (provided by you) if a company , to see that your budget is capable of paying for your purchase.

We have the right to refuse a sale, although we will state why.

Banned Nations:
The Rogue Nation of Gilabad (under the terms of the Warner-McCain Embargo Act)

Products (http://forums.jolt.co.uk/showpost.php?p=10577368&postcount=4)
Services (http://forums.jolt.co.uk/showpost.php?p=10577436&postcount=5)

Rules:
Do your own math. If your math is incorrect, we will add a surcharge of one percent (1%) to the correct total.

All prices are in US Dollars. We will check, using public records thirdgeek - the Public Health and/or Defence or Law & Order sections - if a nation, a link (provided by you) if a company , to see that your budget is capable of paying for your purchase.

We have the right to refuse a sale, although we will state why.

Banned Nations:
The Fascist Republic of Kravania (under the provisions of the Gutierrez-Van Hollen Embargo Act)
The Rogue Nation of Gilabad (under the terms of the Warner-McCain Embargo Act)

Discounts are currently not available.

Products
Services

Wow, lots of Products and Services. :rolleyes:

Wow, lots of Products and Services. :rolleyes:
It takes time to add these things in...this storefront just started, give 'im time....

Panrestoral (c) - Based on antibodies produced against pancreatic cancers, this drug, taken intravenously twice a week for six months, provides an effective means of curing pancreatic cancers without needing to resort to surgery, chemotherapy, or radiation therapy. It has an 88% success rate and is twice as effective as a placebo in recent studies. We sell a six-month package (forty-eight 10cc doses) for $5,400 US and offer 10,000 packages for $50 million US - a savings of $4 million US.

Tryptibit (c) - This drug, taken daily in single 12mg pills, is an easier means of treating asthma than traditional methods. We sell bottles of 60 pills for $120 US; purchase 10,000 bottles for $1 million, a savings of $200,000.

Gene Sequencing - After our success with the Human Genome Project, we have expanded to sequencing other species. Give us DNA samples, two years, and $100,000 US, and our team should be able to provide a map of the genome of the species.

Preimplantation genetic diagnosis: Currently testing for -
Alpha-1-antitrypsin deficiency (AAT; emphysema and liver disease)
Amyotrophic lateral sclerosis (ALS; Lou Gehrig's Disease; progressive motor function loss leading to paralysis and death)
Alzheimer's disease (APOE; late-onset variety of senile dementia)
Ataxia telangiectasia (AT; progressive brain disorder resulting in loss of muscle control and cancers)
Gaucher disease (GD; enlarged liver and spleen, bone degeneration)
Inherited breast and ovarian cancer (BRCA 1 and 2; early-onset tumors of breasts and ovaries)
Hereditary nonpolyposis colon cancer (CA; early-onset tumors of colon and sometimes other organs)
Charcot-Marie-Tooth (CMT; loss of feeling in ends of limbs)
Congenital adrenal hyperplasia (CAH; hormone deficiency; ambiguous genitalia and male pseudohermaphroditism)
Cystic fibrosis (CF; disease of lung and pancreas resulting in thick mucous accumulations and chronic infections)
Duchenne muscular dystrophy/Becker muscular dystrophy (DMD; severe to mild muscle wasting, deterioration, weakness)
Dystonia (DYT; muscle rigidity, repetitive twisting movements)
Fanconi anemia, group C (FA; anemia, leukemia, skeletal deformities)
Factor V-Leiden (FVL; blood-clotting disorder)
Fragile X syndrome (FRAX; leading cause of inherited mental retardation)
Hemophilia A and B (HEMA and HEMB; bleeding disorders)
Hereditary Hemochromatosis (HFE; excess iron storage disorder)
Huntington's disease (HD; usually midlife onset; progressive, lethal, degenerative neurological disease)
Myotonic dystrophy (MD; progressive muscle weakness; most common form of adult muscular dystrophy)
Neurofibromatosis type 1 (NF1; multiple benign nervous system tumors that can be disfiguring; cancers)
Phenylketonuria (PKU; progressive mental retardation due to missing enzyme; correctable by diet)
Adult Polycystic Kidney Disease (APKD; kidney failure and liver disease)
Prader Willi/Angelman syndromes (PW/A; decreased motor skills, cognitive impairment, early death)
Sickle cell disease (SS; blood cell disorder; chronic pain and infections)
Spinocerebellar ataxia, type 1 (SCA1; involuntary muscle movements, reflex disorders, explosive speech)
Spinal muscular atrophy (SMA; severe, usually lethal progressive muscle-wasting disorder in children)
Thalassemias (THAL; anemias - reduced red blood cell levels)
Tay-Sachs Disease (TS; fatal neurological disease of early childhood; seizures, paralysis)

Give us $25 US, the child's karyotype, and one month, and we'll report if the child will be a carrier for, or will have, any of these diseases. For an additional $50 US and an additional week, we'll determine the child's probable future height, eye color, hair color, probable future intelligence, and probable future strength.

Gene Sequencing - After our success with the Human Genome Project, we have expanded to sequencing other species. Give us DNA samples, two years, and $100,000 US, and our team should be able to provide a map of the genome of the species.

Preimplantation genetic diagnosis: Currently testing for -
Alpha-1-antitrypsin deficiency (AAT; emphysema and liver disease)
Amyotrophic lateral sclerosis (ALS; Lou Gehrig's Disease; progressive motor function loss leading to paralysis and death)
Alzheimer's disease (APOE; late-onset variety of senile dementia)
Ataxia telangiectasia (AT; progressive brain disorder resulting in loss of muscle control and cancers)
Gaucher disease (GD; enlarged liver and spleen, bone degeneration)
Inherited breast and ovarian cancer (BRCA 1 and 2; early-onset tumors of breasts and ovaries)
Hereditary nonpolyposis colon cancer (CA; early-onset tumors of colon and sometimes other organs)
Charcot-Marie-Tooth (CMT; loss of feeling in ends of limbs)
Congenital adrenal hyperplasia (CAH; hormone deficiency; ambiguous genitalia and male pseudohermaphroditism)
Cystic fibrosis (CF; disease of lung and pancreas resulting in thick mucous accumulations and chronic infections)
Duchenne muscular dystrophy/Becker muscular dystrophy (DMD; severe to mild muscle wasting, deterioration, weakness)
Dystonia (DYT; muscle rigidity, repetitive twisting movements)
Fanconi anemia, group C (FA; anemia, leukemia, skeletal deformities)
Factor V-Leiden (FVL; blood-clotting disorder)
Fragile X syndrome (FRAX; leading cause of inherited mental retardation)
Hemophilia A and B (HEMA and HEMB; bleeding disorders)
Hereditary Hemochromatosis (HFE; excess iron storage disorder)
Huntington's disease (HD; usually midlife onset; progressive, lethal, degenerative neurological disease)
Myotonic dystrophy (MD; progressive muscle weakness; most common form of adult muscular dystrophy)
Neurofibromatosis type 1 (NF1; multiple benign nervous system tumors that can be disfiguring; cancers)
Phenylketonuria (PKU; progressive mental retardation due to missing enzyme; correctable by diet)
Adult Polycystic Kidney Disease (APKD; kidney failure and liver disease)
Prader Willi/Angelman syndromes (PW/A; decreased motor skills, cognitive impairment, early death)
Sickle cell disease (SS; blood cell disorder; chronic pain and infections)
Spinocerebellar ataxia, type 1 (SCA1; involuntary muscle movements, reflex disorders, explosive speech)
Spinal muscular atrophy (SMA; severe, usually lethal progressive muscle-wasting disorder in children)
Thalassemias (THAL; anemias - reduced red blood cell levels)
Tay-Sachs Disease (TS; fatal neurological disease of early childhood; seizures, paralysis)

Give us $25 US, a sample of the DNA of each of the parents, and one month, and we'll report if the child will be a carrier for, or will have, any of these diseases. For an additional $50 US and an additional week, we'll determine the child's probable future height, eye color, hair color, probable future intelligence, and probable future strength.

[ooc: why don't you just ask for a full karyotype? :D]

OOC - Didn't think of it; edited. Anything else that Celera might reasonably be able to test for in 2016?