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Occludin Protein (OCLN) (His tag)

Dieses Recombinant Occludin-Protein wird in Escherichia coli (E. coli) produziert.
Produktnummer ABIN7669390

Kurzübersicht für Occludin Protein (OCLN) (His tag) (ABIN7669390)

Target

Alle Occludin (OCLN) Proteine anzeigen
Occludin (OCLN)

Protein-Typ

Recombinant

Biologische Aktivität

Inactive

Spezies

  • 8
  • 4
  • 3
Human

Quelle

  • 8
  • 3
  • 2
  • 2
Escherichia coli (E. coli)

Reinheit

> 90 %
  • Aufreinigungstag / Konjugat

    Dieses Occludin Protein ist gelabelt mit His tag.

    Verwendungszweck

    Recombinant Human OCLN Protein(His Tag)

    Sequenz

    Lys266~Thr522

    Aufreinigung

    SDS-PAGE analysis of Human OCLN proteins, 2 μg/lane of Recombinant Human OCLN proteins was resolved with an SDS-PAGE under reducing conditions, showing bands at 28 KD

    Sterilität

    0.2 μm filtered

    Endotoxin-Niveau

    < 10 EU/mg of the protein as determined by the LAL method.
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    Produkt
    Expressionssystem
    Konjugat
    Origin
    Preis ab
    Expressionssystem HEK-293 Cells
    Konjugat His tag
    Origin Human
    Preis ab 16.256,82 €
    Expressionssystem Cell-free protein synthesis (CFPS)
    Konjugat Strep Tag
    Origin Human
    Preis ab 20.480,57 €

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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis.

    Buffer

    Lyophilized from a 0.2 μm filtered solution in PBS with 5 % Trehalose and 5 % Mannitol.

    Lagerung

    4 °C,-20 °C,-80 °C

    Informationen zur Lagerung

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.

    Haltbarkeit

    12 months
  • Target

    Occludin (OCLN)

    Andere Bezeichnung

    OCLN

    Hintergrund

    This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with an simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.,BLCPMG,FLJ08163,FLJ18079,FLJ77961,FLJ94056,MGC34277,Occludin,Ocln,OCLN,Phosphatase 1 regulatory subunit 115,PPP1R115,PTORCH1,Tight junction protein occludin

    Molekulargewicht

    calculated_mw: 28 kDa

    observed_mw: 42 kDa

    UniProt

    Q16625

    Pathways

    Cell-Cell Junction Organization, Hepatitis C
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