Danielson - CT

Finding a Amino Acids Blood Test - 34 Amino Acids in Danielson

This blood test panel measures 34 amino acids, the building blocks of proteins and important intermediates in metabolism. Amino Acids Blood Test - 34 Amino Acids testing in Danielson, CT: order online, visit a patient service center near you, and review your results in a secure account.

Typical price

From $249

Results

1-3 business days

Preparation

See preparation notes below

This blood test panel measures 34 amino acids, the building blocks of proteins and important intermediates in metabolism. It can reveal deficiencies or imbalances that may result from inherited metabolic disorders, liver or kidney disease, nutritional problems, or malabsorption. The panel is used to help diagnose and monitor conditions such as aminoacidurias and organic acidemias and to investigate unexplained metabolic symptoms. Results are interpreted by a specialist alongside clinical findings and other metabolic tests.

• Alanine An amino acid involved in glucose and energy metabolism.
• Alpha-Aminoadipic Acid A metabolite in the lysine breakdown pathway.
• Alpha-Aminobutyric Acid A marker that can reflect amino acid metabolism and liver function.
• Arginine An amino acid involved in the urea cycle and nitric oxide production.
• Asparagine An amino acid important in protein synthesis and nitrogen handling.
• Aspartic Acid An amino acid involved in the urea cycle and energy metabolism.
• Beta-Alanine A metabolite related to the breakdown of pyrimidines and certain amino acids.
• Beta-Aminoisobutyric Acid A breakdown product of thymine and valine metabolism.
• Carnosine A dipeptide of beta-alanine and histidine found in muscle and brain.
• Citrulline An intermediate in the urea cycle that reflects nitrogen processing.
• Cystathionine An intermediate in the transsulfuration pathway of methionine metabolism.
• Cystine A form of cysteine that can indicate sulfur amino acid handling.
• Ethanolamine A compound related to phospholipid metabolism.
• Glutamic Acid An amino acid central to nitrogen metabolism and neurotransmission.
• Glutamine The most abundant amino acid and a key nitrogen carrier.
• Glycine A small amino acid involved in protein synthesis and detoxification.
• Histidine An essential amino acid and precursor to histamine.
• Homocystine A form of homocysteine measured to assess sulfur amino acid metabolism.
• Hydroxyproline A marker related to collagen turnover.
• Isoleucine A branched-chain amino acid used in energy and protein metabolism.
• Leucine A branched-chain amino acid important for protein synthesis.
• Lysine An essential amino acid needed for protein and carnitine synthesis.
• Methionine An essential amino acid and methyl-group donor.
• 3-Methylhistidine A marker of muscle protein breakdown.
• Ornithine An amino acid in the urea cycle.
• Phenylalanine An essential amino acid that is converted to tyrosine.
• Phosphoethanolamine A compound related to phospholipid metabolism.
• Proline An amino acid important in collagen and protein structure.
• Serine An amino acid involved in one-carbon metabolism and protein synthesis.
• Taurine A sulfur-containing compound involved in bile and cellular function.
• Threonine An essential amino acid used in protein synthesis.
• Tryptophan An essential amino acid and precursor to serotonin and niacin.
• Tyrosine An amino acid precursor to thyroid hormone and catecholamines.
• Valine A branched-chain amino acid used in energy and protein metabolism.

• People with symptoms suggesting an inherited metabolic disorder
• Individuals with a family history of metabolic disease
• Patients with unexplained nutritional deficiencies or poor growth
• People with liver or kidney disease affecting amino acid handling
• Patients being monitored for a known amino acid disorder

• Fasting overnight is often required; follow your order instructions
• Avoid a high-protein meal shortly before collection
• Report all medications and nutritional supplements
• Collect the sample in the tube and at the time specified

Abnormal levels of one or more amino acids can indicate an inherited metabolic disorder, a nutritional problem, or organ dysfunction. Specific patterns, such as elevated phenylalanine or low tyrosine, help guide interpretation, but results are complex and are reviewed by a specialist alongside clinical findings and other tests. Discuss your amino acid profile and what it may mean with a healthcare provider.

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