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PROK2 Protein (Transcript Variant 2)

Dieses Recombinant PROK2-Protein wird in Escherichia coli (E. coli) exprimiert.
Produktnummer ABIN2729731

Kurzübersicht für PROK2 Protein (Transcript Variant 2) (ABIN2729731)

Target

Alle PROK2 Proteine anzeigen
PROK2 (Prokineticin 2 (PROK2))

Protein-Typ

Recombinant

Spezies

  • 5
  • 3
  • 3
  • 2
Human

Quelle

  • 10
  • 2
  • 1
Escherichia coli (E. coli)

Applikation

Antibody Production (AbP), Standard (STD)

Reinheit

> 95 % as determined by SDS-PAGE and Coomassie blue staining
  • Proteineigenschaft

    Transcript Variant 2

    Produktmerkmale

    • Recombinant human PROK2 / PK2 (transcript variant 2) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone

    Endotoxin-Niveau

    Endotoxin level is <0.1 ng/μg of protein (<1EU/μg).
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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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    Lyophilized from a 0.2 μM filtered solution of 20 mM phosphate buffer,100 mM NaCl, pH 7.2

    Handhabung

    Resuspend the protein in the desired concentration in proper buffer

    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

    PROK2 (Prokineticin 2 (PROK2))

    Andere Bezeichnung

    Prok2,pk2

    Hintergrund

    This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene.

    Molekulargewicht

    8.8 kDa

    NCBI Accession

    NP_068754
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