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Septin 5 Antikörper

Der Kaninchen Polyklonal anti-Septin 5 Antikörper wird verwendet zum Nachweis von Septin 5 in Proben von Human und Ratte. Er wurde validiert für WB und FACS.
Produktnummer ABIN7882234
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für Septin 5 Antikörper (ABIN7882234)

Target

Alle Septin 5 (SEPT5) Antikörper anzeigen
Septin 5 (SEPT5)

Reaktivität

  • 51
  • 29
  • 11
  • 2
Human, Ratte

Wirt

  • 44
  • 7
Kaninchen

Klonalität

  • 44
  • 6
  • 1
Polyklonal

Konjugat

  • 28
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Septin 5 Antikörper ist unkonjugiert

Applikation

  • 48
  • 24
  • 24
  • 13
  • 13
  • 9
  • 5
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Verwendungszweck

    SEPT5 Antibody / Septin 5

    Sequenz

    HYENYRAHCI QQMTSKLTQD

    Aufreinigung

    Antigen affinity purified

    Immunogen

    Amino acids HYENYRAHCIQQMTSKLTQD were used as the immunogen for the SEPT5 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the SEPT5 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    After reconstitution, the SEPT5 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    Septin 5 (SEPT5)

    Andere Bezeichnung

    SEPT5

    Hintergrund

    This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB, platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.

    UniProt

    Q99719

    Pathways

    Synaptic Vesicle Exocytosis
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