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Recombinant Human DMP1 Protein (His Tag)(Active)– MSE Supplies LLC

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Recombinant Human DMP1 Protein (His Tag)(Active)

SKU: PKSH030969-100

  • £52800
  • Save £5900



Recombinant Human DMP1 Protein (His Tag)(Active)

 

SKU # PKSH030969
Expression Host HEK293 Cells

 

Description

Synonyms ARHP, ARHR, DMP-1, DMP1, Dentin Matrix Acidic Phosphoprotein 1, Dentin Matrix Protein 1
Species Human
Expression Host HEK293 Cells
Sequence Met 1-Tyr 513
Accession Q13316-1
Calculated Molecular Weight 55.4 kDa
Observed Molecular Weight 53 kDa
Tag C-His
Bio-activity Measured by its ability to bind human CFH in a functional ELISA.
  

 

Properties

Purity > 85 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from sterile PBS, pH 7.4
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.


Background

Dentin matrix acidic phosphoprotein (DMP1) is an extracellular matrix protein and a member of the small integrin binding ligand N-linked glycoprotein family. This protein, which is critical for proper mineralization of bone and dentin, is present in diverse cells of bone and tooth tissues. DMP1 contains a large number of acidic domains, multiple phosphorylation sites, a functional arg-gly-asp cell attachment sequence, and a DNA binding domain. In undifferentiated osteoblasts it is primarily a nuclear protein that regulates the expression of osteoblast-specific genes. During osteoblast maturation, DMP1 becomes phosphorylated and is exported to the extracellular matrix, where it orchestrates mineralized matrix formation. Mutations in DMP1 are known to cause autosomal recessive hypophosphatemia, a disease that manifests as rickets and osteomalacia. DMP1 may have a dual function during osteoblast differentiation. In the nucleus of undifferentiated osteoblasts, unphosphorylated form acts as a transcriptional component for activation of osteoblast-specific genes like osteocalcin. During the osteoblast to osteocyte transition phase it is phosphorylated and exported into the extracellular matrix, where it regulates nucleation of hydroxyapatite.