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Cyclin D Binding Myb-Like Transcription Factor 1 (DMTF1) (Middle Region) Peptid

DMTF1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN5512274
  • Target Alle DMP1 (DMTF1) Produkte
    DMP1 (DMTF1) (Cyclin D Binding Myb-Like Transcription Factor 1 (DMTF1))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 10
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    FSRSTGKGGD DKDDDEDDSG DDTFGDDDSG PGPKDRQEGG NSRLGSDEDS
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti- DMP1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    DMP1 (DMTF1) (Cyclin D Binding Myb-Like Transcription Factor 1 (DMTF1))
    Synonyme
    DMP1 Peptide, DMTF Peptide, hDMP1 Peptide, Dimp Peptide, Dmp1 Peptide, DMTF1 Peptide, zgc:92448 Peptide, cyclin D binding myb like transcription factor 1 Peptide, cyclin D binding myb-like transcription factor 1 Peptide, DMTF1 Peptide, Dmtf1 Peptide, dmtf1 Peptide
    Hintergrund
    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.

    Alias Symbols: ARHP, ARHR, DMP-1

    Protein Size: 497
    Gen-ID
    1758
    NCBI Accession
    NM_001079911, NP_001073380
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