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
Storage Conditions
For research use only

-80 ℃

Related Products

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