DMP1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-66956
Catalog Number: E-AB-66956
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IHC,IF
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IHC,IF
Datasheet, Questions? Contact us!
Background:
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.
Research Area: Signal Transduction,Stem Cells,Developmental Biology
Synonyms:
DMP1, ARHP, ARHR, DMP-1
Immunogen: Recombinant fusion protein of human DMP1 (NP_004398.1).
Swissprot: Q13316
Gene ID: 1758
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "IHC 1:50-1:200 IF 1:50-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Signal Transduction,Stem Cells,Developmental Biology
Synonyms:
DMP1, ARHP, ARHR, DMP-1
Immunogen: Recombinant fusion protein of human DMP1 (NP_004398.1).
Swissprot: Q13316
Gene ID: 1758
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "IHC 1:50-1:200 IF 1:50-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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