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Fibrillin 1 antibody

The Rabbit Polyclonal anti-Fibrillin 1 antibody has been validated for IHC and ELISA. It is suitable to detect Fibrillin 1 in samples from Human and Mouse.
Catalog No. ABIN7238018

Quick Overview for Fibrillin 1 antibody (ABIN7238018)

Target

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

Reactivity

  • 67
  • 31
  • 22
  • 11
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human, Mouse

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

  • 61
  • 34
  • 27
  • 19
  • 14
  • 14
  • 13
  • 13
  • 13
  • 11
  • 5
  • 3
  • 2
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human FBN1

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Fibrillin 1 (FBN1)

    Alternative Name

    FBN1

    Background

    This gene encodes a member of the fibrillin family. The encoded protein 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 witHuman, Mousearfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.

    NCBI Accession

    NP_000129

    UniProt

    P35555

    Pathways

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