KeyTec® DDR2, N-GST

Used for Developing DDR2 Biochemical Activity Assay or Binding Assay Models
•  Strict quality control: Each batch comes with a rigorous QC report
•  High activity: Each batch is activity-verified, providing high-quality protein
•  Validated with homogeneous assay models, such as TR-FRET and ADP-Glo, ideal for high-throughput screening

Size: 10 μg100 μg

Price: $ 660

CAT.: P1HI0031S

Delivery: 2-3 weeks

KeyTec® DDR2, N-GST

Used for Developing DDR2 Biochemical Activity Assay or Binding Assay Models

• Strict quality control: Each batch comes with a rigorous QC report • High activity: Each batch is activity-verified, providing high-quality protein • Validated with homogeneous assay models, such as TR-FRET and ADP-Glo, ideal for high-throughput screening

Size: 10 μg100 μg

CAT.: P1HI0031S

Delivery: 2-3 weeks

Price: $ 660

Overview

KeyTec® DDR2, N-GST recombinant protein with N-terminal GST tag + TEV cleavage site was purified by GST affinity and followed by SEC chromatography. The SEC-HPLC result showed that the DDR2 protein was tetramer in the solution. The DDR2 protein (SRC treated) showed high activity in TR-FRET assay.
AA Sequences：	Uniprot: Q16832, R422-E855(end)
Tag：		N-terminal GST tag
Molecular Weight：		75.9 kDa
Species：	Human
Expression Host：	Sf9
Protein Concentration：	0.51 mg/mL by OD280
Purity：>95% by SDS-PAGE
Form：	Liquid
Formulation：	50 mM Tris, 150 mM NaCl, 1 mM DTT, 10% glycerol, 0.05% Brij35, pH7.5

Performance

The DDR2 activity was detected using TR-FRET technology. The reaction was performed by incubating the DDR2 protein, ATP and substrate at 25 ℃ for 60 min, adding the TR-FRET reagents at 25℃ for 60 min, then reading ratio 665/620 by Microplate Reader with TR-FRET.

Protocols

COA_P1HI0031_G130824021_EN.pdf

Components

CAT.

Description

Size

P1HI0031S

KeyTec® DDR2, N-GST

10 μg

Notices

Certificate of Analysis

Limitations

Storage Conditions

For research use only

-80 ℃

Related Products

Overview

KeyTec® DDR2, N-GST recombinant protein with N-terminal GST tag + TEV cleavage site was purified by GST affinity and followed by SEC chromatography. The SEC-HPLC result showed that the DDR2 protein was tetramer in the solution. The DDR2 protein (SRC treated) showed high activity in TR-FRET assay.
AA Sequences：	Uniprot: Q16832, R422-E855(end)
Tag：		N-terminal GST tag
Molecular Weight：		75.9 kDa
Species：	Human
Expression Host：	Sf9
Protein Concentration：	0.51 mg/mL by OD280
Purity：>95% by SDS-PAGE
Form：	Liquid
Formulation：	50 mM Tris, 150 mM NaCl, 1 mM DTT, 10% glycerol, 0.05% Brij35, pH7.5

Performance

The DDR2 activity was detected using TR-FRET technology. The reaction was performed by incubating the DDR2 protein, ATP and substrate at 25 ℃ for 60 min, adding the TR-FRET reagents at 25℃ for 60 min, then reading ratio 665/620 by Microplate Reader with TR-FRET.

Protocols

COA_P1HI0031_G130824021_EN.pdf

Components

CAT.

Description

Size

P1HI0031S

KeyTec® DDR2, N-GST

10 μg

Notices

Certificate of Analysis

Limitations