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ATPlite 1step Luminescence Assay System, 10 mL ATP Assay Kit

ATP luminescence assay for quantitative evaluation of proliferation and cytotoxicity of cultured mammalian cells. The 1step luciferase ATP assay format only requires one addition step, and can be used for continuous processing.

For research use only. Not for use in diagnostic procedures. All products to be used in accordance with applicable laws and regulations including without limitation, consumption and disposal requirements under European REACH regulations (EC 1907/2006).

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Feature Specification
Application Cell Viability
Assay Points 100

ATP luminescence assay for quantitative evaluation of proliferation and cytotoxicity of cultured mammalian cells. The 1step luciferase ATP assay format only requires one addition step, and can be used for continuous processing.

For research use only. Not for use in diagnostic procedures. All products to be used in accordance with applicable laws and regulations including without limitation, consumption and disposal requirements under European REACH regulations (EC 1907/2006).

Click to copy promo code to clipboard.
Save 25% when you buy this product online. Use promo code below.
LITES25
Offer valid until 12/31. Terms and conditions apply.
Product Variants
Unit Size: 10 mL
Part #:
6016736
List Price
USD 87.28
Unit Size: 100 mL
Part #:
6016731
List Price
USD 646.26
Unit Size: 1,000 mL
Part #:
6016739
List Price
USD 4,334.00

Overview

ATP is a marker for cell viability due to its presence in all metabolically active cells. ATP concentration declines rapidly when cells undergo necrosis or apoptosis, and so monitoring ATP is a good indicator of cytotoxic, cytostatic and proliferation effects.

Our ATPlite 1step ATP luminescence assays use patented technologies to measure cell proliferation and cytotoxicity in mammalian cells based on the production of light caused by the reaction of ATP with added luciferase and D-luciferin.

Features and benefits:

  • Simple and reproducible: only one reagent addition step, no separation steps
  • Suitable for both 96- and 384-well microplates
  • Linear correlation between cell number and luminescent signal: up to 50,000 cells per well for 96-well microplates and 12,500 cells per well for 384-well microplates
  • Designed for continuous process systems: luminescence should be measured between 0 and 30 minutes after reagent addition and plate shaking
  • Homogeneous: no cell harvesting or centrifugation required
  • High sensitivity: able to detect down on one cell per well
  • Reduced Phenol Red dependency
  • High light-output: assay can be used with less sensitive luminescence readers such as multi-label readers
  • Fast: no luminescence signal stabilization time required

An alternative format of this assay is also available. The ATPlite assay has separate cell lysis and luminescent signal generation steps. This allows for a more stable signal, with half-life of at least 4 hours.

Specifications

Application
Cell Viability
Assay Points
100
Automation Compatible
Yes
Brand
ATPlite 1step
Cellular or Signaling Pathway
Autophagy
Cell Death
Cell Growth
Cytotoxicity
Necrosis
Cellular Process
Autophagy
Cell Death
Cell Growth
Cytotoxicity
Necrosis
Detection Modality
Luminescence
Format
Microplates
Protocol
1-step
Signal Halflife
0.5 hour
Shipping Conditions
Shipped Ambient
Unit Size
10 mL

Citations

Resources

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Application Note Icon
Application Note
ATPlite assay performance in human primary cells.

In this application note three ATP monitoring luminescence assays were assessed and compared head-to-head: (i) ATPlite™ from...

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Application Note
Proliferation and cell death analyses of 3D cultures using Revvity CellCarrier Spheroid ULA microplates and ATPlite 3D products.

In the process of developing new therapeutic molecules, toxicity – whether it is to be avoided or whether it is desired – is an...

Application Note Icon
Application Note
Simultaneous detection of drug efficacy and toxicity by combining HTRF, AlphaLISA, or AlphaLISA SureFire Ultra with ATPlite

This application note demonstrates how compound’s mechanism of action and potential cytotoxic effects can be deciphered thanks to...

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