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Fibulin 5 antibody

The Rabbit Polyclonal anti-Fibulin 5 antibody has been validated for WB and IF. It is suitable to detect Fibulin 5 in samples from Human and Mouse.
Catalog No. ABIN6572097

Quick Overview for Fibulin 5 antibody (ABIN6572097)

Target

See all Fibulin 5 (FBLN5) Antibodies
Fibulin 5 (FBLN5)

Reactivity

  • 70
  • 40
  • 29
  • 1
Human, Mouse

Host

  • 70
  • 10
  • 1
Rabbit

Clonality

  • 69
  • 14
Polyclonal

Conjugate

  • 41
  • 9
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Fibulin 5 antibody is un-conjugated

Application

  • 64
  • 29
  • 26
  • 16
  • 13
  • 4
  • 4
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human FBLN5 (NP_006320.2).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IF 1:50-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    Fibulin 5 (FBLN5)

    Alternative Name

    FBLN5

    Background

    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3).

    Molecular Weight

    Observed_MW: 70kDa

    Calculated_MW: 50kDa

    Gene ID

    10516

    UniProt

    Q9UBX5

    Pathways

    SARS-CoV-2 Protein Interactome
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