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Collagen, Type IV, alpha 3 (COL4A3) (Middle Region) Peptid

COL4A3 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN975163
  • Target Alle COL4a3 (COL4A3) Produkte
    COL4a3 (COL4A3) (Collagen, Type IV, alpha 3 (COL4A3))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 5
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    YRADDANVVR DRDLEVDTTL KSLSQQIENI RSPEGSRKNP ARTCRDLKMC
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-COL4A3 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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    COL4a3 (COL4A3) (Collagen, Type IV, alpha 3 (COL4A3))
    Synonyme
    zTumstatin Peptide, [a]3(IV) Peptide, alpha3(IV) Peptide, collagen type IV alpha 3 chain Peptide, collagen, type IV, alpha 3 Peptide, COL4A3 Peptide, col4a3 Peptide, Col4a3 Peptide
    Hintergrund
    This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.

    Alias Symbols: -

    Protein Interaction Partner: CAPN1,BGN,BMP1,CAPN1,CD36,CD44,CD93,COL7A1,DCN,DDR2,FGF7,FN1,HTRA1,IGFBP3,ITGA2,ITGA5,MATN2,MMP2,MMP9,NID1,P4HB,PAK1,PDGFB,PRELP,SPARC,TGFBI,THBS1,TMPRSS6,TXN,VWF,COL7A1,IGFBP3,ITGA2,ITGB1,MAG,MATN2,MMP2,NID1,NID2,Nid1,PKD1,PRELP,SPARC,THBS1,TXN,VWF

    Protein Size: 1464
    Molekulargewicht
    137 kDa
    Gen-ID
    1285
    NCBI Accession
    NM_031362, NP_112730
    UniProt
    E7ENN2
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