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Phenylalanine Assay Kit ab83376 provides a quick, simple, accurate method for quantifying phenylalanine in biological samples.

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Functional Studies - Phenylalanine Assay Kit (AB83376), expandable thumbnail
  • Functional Studies - Phenylalanine Assay Kit (AB83376), expandable thumbnail
  • Functional Studies - Phenylalanine Assay Kit (AB83376), expandable thumbnail

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Key facts

Detection method

Fluorescent

Sample types

Urine, Plasma, Tissue Extracts, Serum, Other biological fluids

Assay type

Quantitative

Range

2 - 20 µM

Assay time

60m

Sensitivity

> 2 µM

Associated Products

Select an associated product type

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What's included?

100 Test
Components
Fructose Assay Buffer
1 x 25 mL
Phenyalanine Standard
1 x 1 Vial
Phenylalanine Developer Mix
1 x 1 Vial
Phenylalanine Enzyme Mix
1 x 1 Vial
Tyrosinase
1 x 1 Vial

Recommended products

Phenylalanine Assay Kit ab83376 provides a quick, simple, accurate method for quantifying phenylalanine in biological samples.

Key facts

Detection method

Fluorescent

Sample types

Urine, Plasma, Tissue Extracts, Serum, Other biological fluids

Assay type

Quantitative

Range

2 - 20 µM

Assay time

60m

Assay Platform

Microplate reader

Sensitivity

> 2 µM

Storage

Shipped at conditions

Blue Ice

Appropriate short-term storage conditions

-20°C

Appropriate long-term storage conditions

-20°C

Storage information

-20°C

Notes

Phenylalanine Assay Kit ab83376 provides a quick, simple, accurate method for quantifying phenylalanine in biological samples.

In the phenylalanine assay protocol, phenylalanine is reductively deaminated with the simultaneous formation of NADH which reacts with our fluorescent probe to generate fluorescence at Ex/Em=535/587 nm. The assay is linear in the range from 0.1 to 1.0 nmol (2-20 μM) of Phenylalanine.

Phenylalanine assay protocol summary:
- add samples and standards to wells
- add reaction mix and incubate for 60 min
- analyze with a microplate reader

This product is manufactured by BioVision, an Abcam company and was previously called K572 Phenylalanine Fluorometric Assay Kit. K572-100 is the same size as the 100 test size of ab83376.

L-Phenylalanine (PHE) is an electrically-neutral amino acid, one of the twenty common and one of the three aromatic amino acids used to biochemically form proteins. Phenylalanine uses the same active transport channel as tryptophan to cross the blood-brain barrier, and, in large quantities, interferes with the production of serotonin.

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.

Activity summary

Phenylalanine often abbreviated as Phe is an essential amino acid with a molecular mass of 165.19 g/mol. It serves as a precursor for the biosynthesis of proteins and other compounds. Phenylalanine is transported into cells by a specific membrane transporter and expresses mainly in the liver and brain tissues. In laboratory settings phenylalanine assays and kits are often used to measure its concentration in biological samples which can be colorimetrically or fluorescently assessed.

Biological function summary

Phenylalanine aids in the formation of proteins by incorporating into the polypeptide chains during ribosomal translation. It is not part of a molecular complex but acts as a free amino acid in various cellular processes. Its conversion to tyrosine by the enzyme phenylalanine hydroxylase is an important step in its metabolism. This conversion is necessary because tyrosine is used in the production of neurotransmitters and hormones.

Pathways

Phenylalanine plays an important role in the phenylalanine and tyrosine catabolic pathway. This pathway is critical for the metabolism of aromatic amino acids eventually leading to the synthesis of important compounds like dopamine and norepinephrine. The enzyme phenylalanine hydroxylase closely related to this pathway shows the connection between phenylalanine and subsequent tyrosine-derived neurotransmitters illustrating its importance in neurochemical regulation.

Associated diseases and disorders

Phenylalanine is strongly associated with the genetic disorder phenylketonuria (PKU) resulting from mutations in the phenylalanine hydroxylase gene. This deficiency leads to high levels of phenylalanine in the blood causing neurotoxicity and cognitive impairments if left untreated. Management of PKU involves a diet low in phenylalanine connecting it to medical nutrition strategies. Furthermore high phenylalanine levels can affect proteins involved in neurotransmitter production linking it to potential neurological complications when not properly regulated.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

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3 product images

  • Functional Studies - Phenylalanine Assay Kit (ab83376), expandable thumbnail

    Functional Studies - Phenylalanine Assay Kit (ab83376)

    OEM testing Phase VI ; Kits & Assays Initiative Assay Testing Jan/Feb 2015.

    Phenylalanine measured in cell lysates showing quantities (micromoles) per million of cells tested.

  • Functional Studies - Phenylalanine Assay Kit (ab83376), expandable thumbnail

    Functional Studies - Phenylalanine Assay Kit (ab83376)

    Phenylalanine measured in biofluids showing concentration in micromolar.

  • Functional Studies - Phenylalanine Assay Kit (ab83376), expandable thumbnail

    Functional Studies - Phenylalanine Assay Kit (ab83376)

    Phenylalanine fluorimetric standard curve: mean of duplicates (+/- SD) with background readings subtracted

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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