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Fibrillin 1 Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Fibrillin 1 in WB und ELISA. Er zeigt eine Reaktivität gegenüber Human und Hund.
Produktnummer ABIN2461618

Kurzübersicht für Fibrillin 1 Antikörper (ABIN2461618)

Target

Alle Fibrillin 1 (FBN1) Antikörper anzeigen
Fibrillin 1 (FBN1)

Reaktivität

  • 67
  • 31
  • 23
  • 11
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Hund

Wirt

  • 78
  • 13
  • 1
Kaninchen

Klonalität

  • 80
  • 12
Polyklonal

Konjugat

  • 46
  • 16
  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Fibrillin 1 Antikörper ist unkonjugiert

Applikation

  • 60
  • 35
  • 27
  • 19
  • 14
  • 14
  • 13
  • 13
  • 13
  • 11
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • Aufreinigung

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FBN1.
  • Applikationshinweise

    FBN1 antibody can be used for detection of FBN1 by ELISA at 1:1562500. FBN1 antibody can be used for detection of FBN1 by western blot at 0.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Konzentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handhabung

    As with any antibody avoid repeat freeze-thaw cycles.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FBN1 antibody at -20 °C.
  • Target

    Fibrillin 1 (FBN1)

    Andere Bezeichnung

    FBN1

    Hintergrund

    FBN1 is a member of the fibrillin family. FBN1 is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.

    Molekulargewicht

    21 kDa, 312 kDa

    Gen-ID

    2200

    UniProt

    Q75N89

    Pathways

    Maintenance of Protein Location, SARS-CoV-2 Protein Interaktom
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