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WRNIP1 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

Dieses Recombinant WRNIP1-Protein wird in HEK-293 Cells produziert.
Produktnummer ABIN2715072

Kurzübersicht für WRNIP1 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag) (ABIN2715072)

Target

Alle WRNIP1 Proteine anzeigen
WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))

Protein-Typ

Recombinant

Spezies

  • 2
  • 1
Human

Quelle

  • 1
  • 1
  • 1
HEK-293 Cells

Applikation

Antibody Production (AbP), Standard (STD)

Reinheit

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Proteineigenschaft

    Transcript Variant 2

    Aufreinigungstag / Konjugat

    Dieses WRNIP1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

    Produktmerkmale

    • Recombinant human ATPase WRNIP1 (transcript variant 2) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
  • Möchten Sie weitere Optionen für dieses Protein ?

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    Produkt
    Expressionssystem
    Konjugat
    Origin
    Preis ab
    Expressionssystem HEK-293 Cells
    Konjugat His tag
    Origin Human
    Preis ab 13.711,36 €
    Expressionssystem Cell-free protein synthesis (CFPS)
    Konjugat Strep Tag
    Origin Human
    Preis ab 15.754,29 €

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  • Applikationshinweise

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Lagerung

    -80 °C

    Informationen zur Lagerung

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))

    Andere Bezeichnung

    Atpase Wrnip1

    Hintergrund

    Werner's syndrome is a rare autosomal recessive disorder characterized by accelerated aging that is caused by defects in the Werner syndrome ATP-dependent helicase gene (WRN). The protein encoded by this gene interacts with the exonuclease-containing N-terminal portion of the Werner protein. This protein has a ubiquitin-binding zinc-finger domain in the N-terminus, an ATPase domain, and two leucine zipper motifs in the C-terminus. It has sequence similarity to replication factor C family proteins and is conserved from E. coli to human. This protein likely accumulates at sites of DNA damage by interacting with polyubiquinated proteins and also binds to DNA polymerase delta and increases the initiation frequency of DNA polymerase delta-mediated DNA synthesis. This protein also interacts with nucleoporins at nuclear pore complexes. Two transcript variants encoding different isoforms have been isolated for this gene.

    Molekulargewicht

    69.3 kDa

    NCBI Accession

    NP_569079
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