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PPAR GAMMA COMPETITOR ASSAY EA,A15145,Invitrogen

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订货号 6MK3081
品牌型号 Invitrogen A15145
货期 询货期
最小订货量 1套
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产品介绍 Product Description
规格
Assay Category: Biochemical Assay
Druggable Target: Nuclear Receptors
Label or Dye: Tb (Terbium)
Product Line: LanthaScreen®
Readout: TR-FRET (Binding)
Technique: TR-FRET
Validated Application: Nuclear Receptor Assay
Color: Green
Detection Method: Fluorescent
For Use With (Equipment): Microplate Reader
Format: 384-well plate
储存
Tb-anti-GST Antibody (Rabbit): Store at -20 °C
PPAR gamma-LBD, GST: Store at -80 °C
Fluormone Pan-PPAR Green: Store at -20 °C
TR-FRET PPAR Assay Buffer: Store at 4 °C
1M DTT: Store at -20 °C or -80 °C
描述

This kit contains Rabbit Tb-Anti-GST antibody; other kit components are the same as kit PV4894:

The LanthaScreen® TR-FRET PPAR gamma Competitive Binding Assay provides a sensitive and robust method for high-throughput screening (HTS) of ligands for peroxisome proliferator-activated receptor-gamma (PPAR gamma). The kit uses a terbium-labeled anti-GST antibody, a fluorescent small-molecule pan-PPAR ligand (Fluormone™ Pan-PPAR Green), and human PPAR gamma ligand-binding domain (LBD) that is tagged with glutathione S-transferase (GST) in a homogeneous mix-and-read assay format.

To assay:
When running the LanthaScreen® TR-FRET PPAR gamma Competitive Binding Assay, Fluormone™ Pan-PPAR Green is added to ligand test compounds followed by addition of a mixture of the PPAR gamma-LBD and terbium anti-GST antibody. When the Fluormone™ Pan-PPAR Green is bound to PPAR gamma, energy transfer from the terbium-labeled antibody to the tracer occurs, and a high TR-FRET ratio is observed. Competitive ligand binding to PPAR gamma is detected by a test compound’s ability to displace the tracer, which results in a loss of FRET between the antibody and the tracer. After an incubation period at room temperature, the 520 nm/495 nm TR-FRET ratio is calculated and can be used to determine the IC50 from a dose response curve of the compound (Figure 1). This type of binding assay is analogous to radioligand-based assays, except that it eliminates handling of radioactivity and enables a homogeneous, "addition-only" format.

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