AlphaBiolabs has already successfully partnered with numerous clinics, pharmacies, occupational health services, healthcare providers and medical service providers around the globe.
We deliver a wide range of laboratory testing solutions to suit the needs of your customers and your business, including DNA, drug, alcohol, and health tests.
Our scientists perform all testing in-house at our ISO 17025-accredited laboratory.
Plus, with competitive pricing, rapid turnaround times, and a dedicated account management team on hand, you can be assured you’ll receive the highest standard of service and support from start to finish.
Tests we offer
- DNA– paternity/maternity tests, aunt/uncle tests, grandparent tests, sibling tests, twin tests, prenatal paternity tests, prenatal gender tests, Y-chromosome tests and more
- Drugs– oral fluid (saliva), urine, hair, and nail samples analyzed
- Alcohol– hair, breath, blood, and nail samples analyzed
- Health– including our Celiac Genetic Test and Genetic Lactose Intolerance Test
Call our Partners team on 727-325-2902 or email partners@alphabiolabs.com to discuss your requirements.
Why partner with AlphaBiolabs?
- Competitive pricing
- Rapid results
- Dedicated account management team
- All testing carried out at our ISO 17025 and BBB-accredited laboratory
- Choose end-to-end laboratory testing, analysis, and reporting – or tell us which services you need
- Trusted partner of numerous clinics, pharmacies, and occupational health services, as well as major healthcare and medical service providers worldwide
Complete the form above to find out more.
Alternatively, call our Partners team on 727-325-2902 or email partners@alphabiolabs.com to discuss your needs.
Our services
DNA testing
We are a leading provider of DNA testing and use the very latest techniques in DNA analysis to help people verify biological relationships between family members.
We offer a comprehensive range of DNA relationship tests direct from our ISO 17025-accredited laboratory, including paternity, non-invasive prenatal paternity (NIPP), maternity, sibling, grandparent, aunt or uncle (avuncular), cousin, twin, Y chromosome, single genetic profile, and viability testing.
Non-invasive prenatal paternity (NIPP) test
An AlphaBiolabs non-invasive prenatal paternity (NIPP) test can be performed as early as 7 weeks into pregnancy and is used to determine the identity of a child’s biological father while the mother is still pregnant.
The test is 100% risk free for mother and baby, with only cheek swabs required from the potential father, plus cheek swabs and a blood sample from the mother.
Our prenatal paternity testing uses a state-of-the-art process that combines the latest DNA technology and unique methods of preserving the baby’s DNA, which is naturally found in the mother’s bloodstream from 7 weeks into pregnancy.
Extended carrier screening
An AlphaBiolabs extended carrier screening test is a back-to-lab test that can tell individuals their genetic carrier status for over 418 recessive inherited disorders.
Although each genetic disorder is rare in itself, there are hundreds of such disorders.
The test is non-invasive, with only a simple cheek swab sample required, and uses a scientific process called Next Generation Sequencing (NGS) to investigate gene mutations (variants) that are known to cause rare genetic disorders.
Prenatal gender test
An AlphaBiolabs Prenatal Gender Test can be performed as early as 6 weeks into pregnancy and is used to determine the gender of an unborn baby while the mother is still pregnant.
The test is 100% risk free for mother and baby, with only a blood sample required from the mother.
Our Prenatal Gender Test uses state-of-the-art processes to determine whether any Y-chromosomal DNA is present in the mother’s blood sample. If a Y chromosome is present, this indicates that the baby is a boy. If no Y chromosome is present, this indicates that the baby is a girl.
Drug testing
Employing some of the foremost toxicology scientists in their field, our accredited toxicology laboratory uses the most up-to-date technology to detect a wide range of drugs and their metabolites.
We can establish whether an individual has been misusing drugs during a defined period of up to 12 months.
Our laboratory can test a wide range of biological samples for the presence of drugs and their metabolites, including oral fluid (saliva), urine, head hair, body hair and nail clippings.
Alcohol testing
AlphaBiolabs’ alcohol testing is carried out at our state-of-the-art toxicology laboratory.
We can establish whether an individual has been misusing alcohol during a defined period of up to 12 months.
Our toxicology scientists can test a wide range of biological samples including head hair, body hair, blood, nails and breath, for a historic or real-time insight into an individual’s alcohol consumption.
Celiac Genetic Test
An AlphaBiolabs Celiac Genetic Test is a fast, accurate back-to-lab test that can tell individuals whether they carry the genes linked to celiac disease.
Celiac disease is an autoimmune disease that develops over time because of a sensitivity to gluten, a protein found in certain cereal grains including wheat, rye, and barley, and commonly used in food products including bread, cereal, and pasta.
The disease runs in families and can start at any age, making genetic testing an extremely useful tool for determining whether an individual is at risk of developing the condition.
Our Celiac Genetic Test is non-invasive, with only a cheek swab sample required, and uses Human Leukocyte Antigen (HLA) typing to confirm or rule out the potential of developing celiac disease by analyzing six DNA markers for the HLA-DQ2 and HLA-DQ8 genes.
This test cannot be used to diagnose celiac disease but can be used to either confirm or rule out the risk of developing the condition in the future.
Genetic Lactose Intolerance Test
Primary lactose intolerance is the most common form of lactose intolerance worldwide.
An AlphaBiolabs Genetic Lactose Intolerance Test is a fast and accurate back-to-lab test that can tell individuals whether they carry the gene variations linked to primary lactose intolerance.
Lactose intolerance is a common digestive issue where the body fails to produce enough of the lactase enzyme. The lactase enzyme is required to break down lactose, the sugar mainly found in dairy products such as milk.
Our genetic lactose intolerance test is non-invasive, with only a simple cheek swab sample required. Our in-house scientists will analyze the cheek swab DNA sample to look for changes (mutations/variations) at specific locations of the MCM6 gene – the gene that helps regulate the production of the lactase enzyme.
If variations are detected, this indicates that the individual has primary lactose intolerance, and can therefore seek the correct diagnosis and treatment.