EnzyChrom™ L-Alanine Assay Kit

SKU:BHT15600117
Suppliers
BioAssay Systems
BioAssay Systems
Details Products
Overview
Click light‑blue chips for details
EnzyChrom L-Alanine Assay Kit is designed for quantitative determination of L-Alanine and evaluation of drug effects on alanine metabolism. It uses OD570 nm, or FL530/585 nm readout; suited to plasma, serum, urine; typical assay time 60 min; detection limit 0.4 µM.
Detection method Colorimetric (OD 570 nm) or Fluorescent (FL 530/585 nm)
Sample type Plasma, serum, urine, tissue and culture media
Species All species
Procedure 60 min
Detection limit 0.4 µM
Options selector
Catalog no. Size
EALA-100 100 Tests
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 100 Tests
  • Lead time: varies by selected option; please contact us for current fulfillment timing.
  • Storage: -20°C — Store at -20°C (freezer). Avoid repeated freeze-thaw cycles.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No EALA-100
Assay Time
  • 60 min
Detection Method
  • Colorimetric (OD 570 nm) or Fluorescent (FL 530/585 nm)
Product Type
  • Assay Kits
  • Amino Acids & Proteins
Sample Type(s) Plasma, serum, urine, tissue and culture media
Shipping Cold pack (ICE) — Ships on ice (cold pack included). Store immediately upon receipt.
Species All
Storage -20°C — Store at -20°C (freezer). Avoid repeated freeze-thaw cycles.

Overview

For quantitative determination of L-Alanine and evaluation of drug effects on alanine metabolism. The assay uses OD570nm, or FL530/585nm for signal readout. Compatible sample input includes Plasma, serum, urine, tissue and culture media. Typical stated assay timing is 60 min.

Key elements and design rationale

  • Readout format: OD570nm, or FL530/585nm supports plate-based signal acquisition and consistent comparison across matched samples.
  • Sample compatibility: The stated sample scope includes Plasma, serum, urine, tissue and culture media, which is useful when aligning matrix type with calibration and control design.
  • Analytical range context: The supplied specifications include a stated detection limit of 0.4 µM for interpreting low-signal samples.

Available format information for this listing includes 100 Tests.

Biological background

This product is centered on measurement of l-alanine within the matrices described for the assay. In practice, datasets from this type of format are typically interpreted by comparing relative signal, activity, or abundance across matched control and experimental groups rather than relying on a single value in isolation. Careful alignment of sample matrix, incubation window, and calibration strategy is important when comparing results across plates, operators, or study days.

More details

ALANINE , a nonessential amino acid, is utilized in the glucose-alanine cycle between tissues and the liver. In tissues that metabolize amino acids, amino groups are collected as glutamate by transamination. The amine group is then transferred by alanine transaminase (ALT) from glutamate to pyruvate to form alanine and a-ketoglutarate. The alanine generated is transported to the liver where a reverse ALT reaction occurs and pyruvate is regenerated. Pyruvate is converted through gluconeogenesis to glucose which can then be recirculated to the tissues. Alanine concentration may have some correlation with high blood pressure, energy intake, cholesterol levels and body mass index. BioAssay Systems’ Alanine Assay Kit provides a simple, direct and automation-ready procedure for measuring alanine concentration. Alanine is converted into pyruvate which can then be directly measured. The color intensity of the reaction product at 570nm or fluorescence intensity at λex/em = 530/585nm is directly proportional to the alanine concentration in the sample.

Detection method

Colorimetric (OD 570 nm) or Fluorescent (FL 530/585 nm).

Detection limit and analytical sensitivity

Reported detection limit: 0.4 µM.

Procedures and timing

Stated procedure or timing information: 60 min.

Research relevance and current trends

  • Plate-based quantification and side-by-side group comparison remain central use cases for this assay format.
  • The description supports intervention-focused study designs in which researchers compare baseline and perturbed conditions.
  • Short assay timing and plate compatibility support time-course or repeated-measure collection plans when handling is kept consistent.

Common research applications

  • Quantify l-alanine in plasma, serum, urine by OD570 nm, or FL530/585 nm readout.
  • Compare treatment or phenotype groups using matched plasma, serum, urine handling.
  • Monitor time-course or pre/post changes in plasma, serum, urine across study conditions.

Interpretation is usually strongest when signal changes are assessed alongside matrix-matched controls, replicate agreement, and the assay's stated analytical window.

Notes for experimental interpretation

  • Matrix composition, background signal, and sample handling can influence apparent response; compare like-with-like whenever possible.
  • Use appropriate blanks, controls, and replicate wells to distinguish biological differences from plate, reagent, or handling variability.

For laboratories requiring additional technical capacity, we provide scientific support services including assay execution, method guidance, product sourcing, and customization to align the assay with specific experimental objectives. If you need assistance selecting the appropriate kit configuration, adapting the workflow to your application, or identifying related research services, please click Talk to a Scientist, email support@biohippo.com, or review our Research Services; a member of our scientific team will follow up with recommendations tailored to your study.

The effects of alanine on glucose metabolism in rainbow trout: Integration of glucose fluxes and molecular evidence [Thesis, Universite d’Ottawa / University of Ottawa]

Jubouri, M. (2020). The effects of alanine on glucose metabolism in rainbow trout: Integration of glucose fluxes and molecular evidence [Thesis, Universite d’Ottawa / University of Ottawa]. Assay: L-alanine in fish plasma.

Get a Quote

Please use this form for bulk quantity requests or customized products.

Contact Information

Product Information

Try Celltrypse Free – Request Your Sample Today

Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

Try Celltrypse Free – Request Your Sample Today

Try Celltrypse Free – Request Your Sample Today

Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

Try Celltrypse Free – Request Your Sample Today