ALK2 (ACVR1) (Q207D), GST-Tag Recombinant

Catalog #
101936
$435 *
Size: 10 µg
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Description

Recombinant human ALK2 (Q207D) (activin receptor-like kinase-2), encompassing amino acids 147-end with a Q207D mutation. This construct contains an N-terminal GST-tag. The recombinant protein was affinity purified and is active.

Synonyms
Activin receptor-like kinase 2, ACTR-I, ALK-2, SKR1, TSR-I, ACVR1, ACVRLK2
Product Info
Storage and Usage
Citations
Species
Human
Construct
ALK2 (Q207D) (GST-147-end)
Mutation
Q207D
Host Species/Expression System
Sf9
Purity

≥90% (Purity calculation does not include co-purifying Glutathione-binding proteins.)

Format

Aqueous buffer solution

Formulation

50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 10 mM Glutathione, 0.1 mM EDTA, 0.25 mM DTT, 0.1 mM PMSF, 25% glycerol

MW
67 kDa
Amino Acids
147-end
Specific Activity

18 pmol/min/µg

Genbank #
NM_001105
UniProt #
Q04771
Tag(s)
N-terminal GST-tag
Background

ALK2 (activin receptor-like kinase 2), also known as ACVR1 or activin A receptor type 1, is a bone morphogenic protein receptor involved in BMP (bone morphogenic protein) signal transduction. ALK2 forms complexes with BMPs, which then recruit proteins from the SMAD family (Mothers against decapentaplegic homolog). It participates in the development and regulation of the skeletal system, heart, brain and reproductive system. ALK2 dysfunction can lead to fibrodysplasia ossificans progressive (FOP), where the BMP/SMAD pathway is hyper-activated and mesenchymal stem cells differentiate along the osteogenic pathway and transform into bone all over the body. Mutations in ALK2 were also found in cancer, such as diffuse intrinsic pontine glioma (DIPG) and child brain cancer. ALK2 inhibitors have been studied in pre-clinical models of FOP and DIPG and showed great promise. Further studies into ALK2 will deepen our understanding of its functions, find new inhibitors and new therapeutic avenues for patients with ALK-linked cancer.