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Fibrillin 1 antibody

This Rabbit Polyclonal antibody specifically detects Fibrillin 1 in WB and ELISA. It exhibits reactivity toward Human and Dog.
Catalog No. ABIN2461618

Quick Overview for Fibrillin 1 antibody (ABIN2461618)

Target

See all Fibrillin 1 (FBN1) Antibodies
Fibrillin 1 (FBN1)

Reactivity

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

Host

  • 78
  • 13
  • 1
Rabbit

Clonality

  • 80
  • 12
Polyclonal

Conjugate

  • 46
  • 16
  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Fibrillin 1 antibody is un-conjugated

Application

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

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

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

    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.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handling Advice

    As with any antibody avoid repeat freeze-thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    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)

    Alternative Name

    FBN1

    Background

    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.

    Molecular Weight

    21 kDa, 312 kDa

    Gene ID

    2200

    UniProt

    Q75N89

    Pathways

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