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V7001_ADP-Glo--Max-Assay--1-000-Assays_3 V7002_ADP-Glo--Max-Assay--10-000-Assays_3

Luminescent Method to Measure ATPase or Kinase Activity

  • Screen library compounds for effects on target enzymes
  • Perform mode of action studies on enzymes of interest
  • Measure activity of immunoprecipitated ATPases/kinases
  • Use when higher ATP concentration is required (up to 5mM)

Catalog Number:

Size

Catalog Number: V7001

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Catalog Number: V7002

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Overview
Protocols
Specifications
Resources
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The ADP-Glo™ Max Assay is a luminescent ADP detection assay that provides a universal, homogeneous, high-throughput screening method to measure ATPase or kinase activity by quantifying the amount of ADP produced in a reaction. The assay can be used to monitor the activity of virtually any ADP-generating enzyme (e.g., kinase or ATPase) when higher ATP concentration is required (up to 5mM). The ADP-Glo™ Max Assay produces a strong signal that positively correlates with enzyme activity and can be adapted to a multitude of plate formats.

The assay is performed in two steps: first, after the completion of the ADP-producing reaction, an equal volume of ADP-Glo™ Reagent is added to terminate the reaction and deplete the remaining ATP. Second, the ADP-Glo™ Max Detection Reagent is added to simultaneously convert ADP to ATP, and the latter is converted to light in a coupled reaction with luciferase/luciferin.

The ADP-Glo™ Max Assay has a high dynamic range and produces a strong signal at low ATP to ADP conversion, making it well suited for screening low-activity ATPases such as drug membrane transporters and heat shock proteins. The assay produces minimal false hits and Z´ values of greater than 0.7.

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  • High signal strength at low ATP conversion makes the assay well suited for low-activity ATPases/kinases.
  • Sensitive to low concentrations of ADP, requiring less enzyme than other assays.
  • Use with virtually with any ADP-producing enzyme—enables researchers to screen a wider range of enzymes using a single platform.
  • Can be used at ATP concentrations up to 5mM, important for enzymes with high Kam values for ATP and for mode of action studies.
  • Accurately measures ADP levels at a wide range of starting ATP concentrations; users assured that activity measured truly reflects enzyme activity and produces accurate IC50 values comparable to radioactivity-based assays.

The ADP-Glo™ Max Assays contain enough reagent to perform the indicated number of reactions in 384-well format using 5μl, 5μl and 10μl of an enzyme reaction, ADP-Glo™ Reagent and ADP-Glo™ Max Detection Reagent, respectively, per sample.

8051MB-W

Principle of the ADP-Glo™ Max Assay. The assay is performed in two steps: 1) after the ATPase or kinase reaction, ADP-Glo™ Reagent is added to terminate the reaction and deplete the remaining ATP; and 2) the ADP-Glo™ Max Detection Reagent is added to convert ADP to ATP and allow the newly synthesized ATP to be measured using a luciferase/luciferin reaction. The light generated correlates to ADP present and ATPase activity.

Specifications

Catalog Number:

Contenido

Item Part # Presentación

ADP-Glo™ Max Detection Buffer

V701A 1 × 10ml

ADP-Glo™ Max Detection Substrate

V702A 1 × 1 vial

Ultra Pure ATP, 100mM

V703A 1 × 250μl

ADP-Glo™ Reagent

V912A 1 × 5ml

ADP, 10mM

V916A 2 × 500μl

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Use Restrictions

For Research Use Only. Not for Use in Diagnostic Procedures.

Condiciones de Almacenaje

BB

 

Patentes y Exclusiones

U.S. Pat. No. 7,700,310 and other patents and patents pending.

U.S. Pat. No. 8,183,007 and other patents and patents pending.

Contenido

Item Part # Presentación

ADP-Glo™ Max Detection Buffer

V701B 1 × 100ml

ADP-Glo™ Max Detection Substrate

V702B 1 × 1 vial

Ultra Pure ATP, 100mM

V703B 1 × 2.5ml

ADP-Glo™ Reagent

V912B 1 × 50ml

ADP, 10mM

V916B 1 × 5ml

Certificado de Análisis

Search by lot number

Use Restrictions

For Research Use Only. Not for Use in Diagnostic Procedures.

Condiciones de Almacenaje

BB

 

Patentes y Exclusiones

U.S. Pat. No. 7,700,310 and other patents and patents pending.

U.S. Pat. No. 8,183,007 and other patents and patents pending.

Resources

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