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Siglec E Protein (AA 20-355, C-Term) (Fc Tag)

Siglece Spezies: Maus Wirt: HEK-293 Cells Recombinant > 95 % , as determined by Coomassie stained SDS-PAGE. FACS, IHC Active
Produktnummer ABIN2666859
  • Target Alle Siglec E (Siglece) Produkte
    Siglec E (Siglece) (Sialic Acid Binding Ig-Like Lectin E (Siglece))
    Protein-Typ
    Recombinant
    Biologische Aktivität
    Active
    Proteineigenschaft
    AA 20-355, C-Term
    Spezies
    Maus
    Quelle
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses Siglec E Protein ist gelabelt mit Fc Tag.
    Applikation
    Flow Cytometry (FACS), Immunohistochemistry (IHC)
    Reinheit
    > 95 % , as determined by Coomassie stained SDS-PAGE.
    Sterilität
    0.22 μm filtered
    Endotoxin-Niveau

    Less than 1.0 EU per μg of protein as determine by the LAL method.

  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Kommentare

    Biological activity: Recombinant mouse Siglec E is able to agglutinate human red blood cells with an ED50 of 0.625 - 2.5 μg/ml.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Rekonstitution
    For maximum results, quick spin vial prior to opening. Stock solutions should be prepared at no less than 10 μg/mL in sterile buffer (PBS, HPBS, DPBS, and EBSS) containing carrier protein such as 1 % BSA or HSA. After dilution, the cytokine can be stored between 2 °C and 8 °C for one month or from -20 °C to -70 °C for up to 3 months.
    Konzentration
    100 μg/mL
    Buffer
    0.22 μm filtered protein solution is in PBS.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Unopened vial can be stored between 2°C and 8°C for three months, at -20°C for six months, or at -70°C for one year.
  • Target
    Siglec E (Siglece) (Sialic Acid Binding Ig-Like Lectin E (Siglece))
    Andere Bezeichnung
    Siglec E (Siglece Produkte)
    Synonyme
    Cd170 Protein, Siglec12 Protein, Siglec5 Protein, Siglec9 Protein, Siglecl1 Protein, mSiglec-E Protein, sialic acid binding Ig-like lectin E Protein, Siglece Protein
    Hintergrund
    Siglecs (sialic acid binding Ig-like lectins) are type I membrane proteins with an extracellular region containing a sialic acid binding V-set Ig-like domain at the N-terminus, followed by varying numbers of C2-set Ig domains. The cytoplasmic tails of all siglecs have one or more tyrosines within potential signalling motifs. Siglecs are widely expressed on hematopoietic cells, often in a cell-type-specific manner. Their ligands, sialic acids, are negatively charged monosaccharides found on cell-surface glycoproteins and glycolipids. Studies suggest that siglecs may participate in cell-cell interactions or act as receptors for the entry of viral or bacterial pathogens. In addition, the presence of immunoreceptor tyrosine-based inhibitory motifs (ITIM) in their cytoplasmic domain indicates that these molecules may play a role in the suppression of immunoreceptor signaling. The siglecs can be classified into two subgroups, with Siglec-1, -2, and -4 as one group and a Siglec-3/CD33-related subgroup (Siglec-3, and -5 through -13) as the second. Siglec E is a mouse CD33-related siglec that selectively regulates early recruitment of neutrophils to the lung in acute lung inflammation induced by lipopolysaccharide. Siglec E-deficient mice exhibit exaggerated neutrophil recruitment that is reversible by using a blockade of the β2 integrin, CD11b. In addition, sialidase treatment of fibrinogen reverses the suppressive effect of Siglec E on CD11b signaling, suggesting that sialic acid recognition by Siglec E is required for its inhibitory function. These findings indicate that Siglec E is an important negative regulator of neutrophil recruitment to the lung and β2 integrin-dependent signaling.
    Molekulargewicht
    This 570 amino acid recombinant protein has a predicted molecular mass of approximately 63 kDa. The protein migrates at about 80 - 90 kDa by SDS-PAGE in DTT-reducing conditions and about 180 - 200 kDa in non-reducing conditions. The predicted N-terminal a
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