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LZTFL1 Protein (Myc-DYKDDDDK Tag)

Dieses Recombinant LZTFL1-Protein wird in HEK-293 Cells produziert.
Produktnummer ABIN2725086

Kurzübersicht für LZTFL1 Protein (Myc-DYKDDDDK Tag) (ABIN2725086)

Target

Alle LZTFL1 Proteine anzeigen
LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))

Protein-Typ

Recombinant

Spezies

  • 4
  • 2
  • 1
  • 1
  • 1
Human

Quelle

  • 3
  • 2
  • 2
  • 1
  • 1
HEK-293 Cells

Applikation

Antibody Production (AbP), Standard (STD)

Reinheit

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Aufreinigungstag / Konjugat

    Dieses LZTFL1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

    Produktmerkmale

    • Recombinant human LZTFL1 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 11.737,02 €
    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

    LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))

    Andere Bezeichnung

    Lztfl1

    Hintergrund

    This gene encodes a ubiquitously expressed protein that localizes to the cytoplasm. This protein interacts with Bardet-Biedl Syndrome (BBS) proteins and, through its interaction with BBS protein complexes, regulates protein trafficking to the ciliary membrane. Nonsense mutations in this gene cause a form of Bardet-Biedl Syndrome a ciliopathy characterized in part by polydactyly, obesity, cognitive impairment, hypogonadism, and kidney failure. This gene may also function as a tumor suppressor possibly by interacting with E-cadherin and the actin cytoskeleton and thereby regulating the transition of epithelial cells to mesenchymal cells. Alternative splicing of this gene results in multiple transcript variants.

    Molekulargewicht

    34.4 kDa

    NCBI Accession

    NP_065080
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