SRP0245
DYRK2 Active human
recombinant, expressed in baculovirus infected insect cells, ≥50% (SDS-PAGE)
别名:
dual specificity tyrosine-phosphorylation-regulated kinase 2
产品名称
DYRK2 Active human, recombinant, expressed in baculovirus infected insect cells, ≥50% (SDS-PAGE)
biological source
human
recombinant
expressed in baculovirus infected insect cells
assay
≥50% (SDS-PAGE)
form
aqueous solution
mol wt
63.5 kDa
packaging
pkg of 10 μg
concentration
>0.02 mg/mL
NCBI accession no.
UniProt accession no.
shipped in
dry ice
storage temp.
−70°C
Gene Information
human ... DYRK2(8445)
Application
Useful for the study of enzyme kinetics, screening inhibitors, and selectivity profiling.
General description
Human DYRK2 (GenBank Accession No. NM_003583), full length with N-terminal His tag, MW = 63.5 kDa, expressed in Baculovirus infected Sf9 cell expression system.
Physical form
TBST+20% glycerol+3mM DTT
Preparation Note
Thaw on ice. Upon first thaw, briefly spin tube containing enzyme to recover full content of the tube. Aliquot enzyme into single use aliquots. Store remaining undiluted enzyme in aliquots at -70°C. Note: Enzyme is very sensitive to freeze/thaw cycles.
法规信息
新产品
此项目有
Rosario Morrugares et al.
Cellular and molecular life sciences : CMLS, 77(13), 2621-2639 (2019-10-13)
NOTCH proteins constitute a receptor family with a widely conserved role in cell cycle, growing and development regulation. NOTCH1, the best characterised member of this family, regulates the expression of key genes in cell growth and angiogenesis, playing an essential
Isao Kii et al.
Nature communications, 7, 11391-11391 (2016-04-23)
Autophosphorylation of amino-acid residues is part of the folding process of various protein kinases. Conventional chemical screening of mature kinases has missed inhibitors that selectively interfere with the folding process. Here we report a cell-based assay that evaluates inhibition of
Martin Mehnert et al.
Nature communications, 11(1), 3563-3563 (2020-07-18)
Rapidly increasing availability of genomic data and ensuing identification of disease associated mutations allows for an unbiased insight into genetic drivers of disease development. However, determination of molecular mechanisms by which individual genomic changes affect biochemical processes remains a major
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