Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

WFS1 Antikörper (AA 272-876)

Der Kaninchen Polyklonal anti-WFS1 Antikörper (ABIN7873171) detektiert spezifisch WFS1 in WB und ELISA. Dieser Antikörper reagiert spezifisch mit Proben aus Human.
Produktnummer ABIN7873171
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für WFS1 Antikörper (AA 272-876) (ABIN7873171)

Target

Alle WFS1 Antikörper anzeigen
WFS1 (Wolfram Syndrome 1 (WFS1))

Reaktivität

  • 39
  • 8
  • 5
  • 3
Human

Wirt

  • 36
  • 4
Kaninchen

Klonalität

  • 36
  • 4
Polyklonal

Konjugat

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser WFS1 Antikörper ist unkonjugiert

Applikation

  • 33
  • 13
  • 13
  • 13
  • 9
  • 5
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • Bindungsspezifität

    • 15
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 272-876

    Verwendungszweck

    WFS1 Antibody / Wolframin

    Aufreinigung

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids D272-K876) was used as the immunogen for the WFS1 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the WFS1 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 WFS1 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

    WFS1 (Wolfram Syndrome 1 (WFS1))

    Andere Bezeichnung

    WFS1

    Hintergrund

    Wolframin is a protein that in humans is encoded by the WFS1 gene. This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene.

    UniProt

    O76024

    Pathways

    Sensory Perception of Sound, Carbohydrate Homeostasis, ER-Nucleus Signaling, Negative Regulation of intrinsic apoptotic Signaling, SARS-CoV-2 Protein Interaktom
Sie sind hier:
Chat with us!