Human Dentin Matrix Acidic Phosphoprotein 1 (DMP1) Protein

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208€ (10 µg)

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935106861
info@markelab.com
name
Human Dentin Matrix Acidic Phosphoprotein 1 (DMP1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx690503
tested applications
SDS-PAGE

Description

Human Dentin Matrix Acidic PhosphoProtein is a recombinant protein from Human produced in Human Cells. Recombinant Human Dentin matrix protein 1 is produced by our Mammalian expression system and the target gene encoding Lys17-Tyr513 is expressed with a 6His tag at the C-terminus.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
Dentin Matrix Acidic PhosphoProtein
Host
Human
Origin
Human
Observed MW
Molecular Weight: 55 kDa

Sequence Fragment: Lys17-Tyr513

Tag: C-terminal 6 His tag
Expression
Recombinant
Purity
> 95% (SDS-PAGE)
Size 1
10 µg
Size 2
50 µg
Form
Lyophilized
Tested Applications
SDS-PAGE
Buffer
20mM PB, 150mM NaCl, pH7.4.
Availability
Shipped within 5-15 working days.
Storage
Store at < -20°C.
Dry Ice
No
UniProt ID
Q13316
Background
Protein DMP1
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

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Dentin matrix acidic phosphoprotein 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. The protein 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 the protein becomes phosphorylated and is exported to the extracellular matrix, where it orchestrates mineralized matrix formation. Mutations in the gene are known to cause autosomal recessive hypophosphatemia, a disease that manifests as rickets and osteomalacia. The gene structure is conserved in mammals. Two transcript variants encoding different isoforms have been described for this gene.

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