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Lysine Assay Kit (Fluorometric) (ab273311)

Lysine Assay Kit (Fluorometric) (ab273311)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Assay type: Quantitative
  • Detection method: Fluorescent
  • Platform: Microplate
  • Sample type: Cell Lysate, Plasma, Serum, Tissue Homogenate
  • Sensitivity: 5 µM

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Overview

  • Product name

    Lysine Assay Kit (Fluorometric)
  • Detection method

    Fluorescent
  • Sample type

    Serum, Plasma, Cell Lysate, Tissue Homogenate
  • Assay type

    Quantitative
  • Sensitivity

    5 µM
  • Assay duration

    Multiple steps standard assay
  • Product overview

    Lysine Assay Kit (Fluorometric) (ab273311) allows the highly sensitive quantification of L-lysine levels in various biological samples. The assay is based on the selective enzymatic metabolism of lysine, yielding an oxidized intermediate which reacts with a fluorogenic probe to form a stable fluorophore (Ex/Em = 538/587 nm). The assay is not affected by the physiological concentration of other amino acids and is high-throughput adaptable.


    The kit can detect less than 5 μM Lysine in samples.

  • Notes

    Abcam has not and does not intend to apply for the REACH Authorisation of customers’ uses of products that contain European Authorisation list (Annex XIV) substances.
    It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

  • Platform

    Microplate

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 100 tests
    Developer Mix (Lyophilized) 1 vial
    Lysine Assay Buffer 1 x 25ml
    Lysine Enzyme Mix (Lyophilized) 1 vial
    Lysine Probe 1 x 200µl
    Lysine Standard (Lyophilized) 1 vial

Images

  • Specificity for detection of L-Lysine (LYS) over other common amino acids.
    Specificity for detection of L-Lysine (LYS) over other common amino acids.

    At a 10-fold molar excess (10 nmole/well) versus L-Lysine (1 nmole/well), all other amino acids tested contributed ≤10% interference.

  • Estimation of total L-Lysine in pooled normal human plasma, single donor off-the-clot human serum, single donor human saliva and cell culture growth medium.
    Estimation of total L-Lysine in pooled normal human plasma, single donor off-the-clot human serum, single donor human saliva and cell culture growth medium.

    Estimation of total L-Lysine in pooled normal human plasma (5 μL/well), single donor off-the-clot human serum (5 μL/well), single donor human saliva (5 μL/well) and cell culture growth medium (DMEM/F12 with 10% FBS, 2 μL/well).

    L-Lysine concentrations for plasma, serum and saliva samples were 185.7 ± 24.9 μM, 195.1 ± 28.9 μM and 14.03 ± 1.31 μM, respectively, whereas the concentration for DMEM/F12 culture medium was 518.6 ± 32.4 μM. Data are mean ± SD of at least 3 replicates. Samples were deproteinized using 10 kDa MWCO spin columns and assayed according to the kit protocol.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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