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LOXL1 antibody

The Rabbit Polyclonal anti-LOXL1 antibody has been validated for IF. It is suitable to detect LOXL1 in samples from Human, Mouse and Rat.
Catalog No. ABIN6566806

Quick Overview for LOXL1 antibody (ABIN6566806)

Target

See all LOXL1 Antibodies
LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

Reactivity

  • 56
  • 22
  • 9
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 60
  • 7
Rabbit

Clonality

  • 62
  • 5
Polyclonal

Conjugate

  • 36
  • 11
  • 10
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LOXL1 antibody is un-conjugated

Application

  • 46
  • 26
  • 19
  • 18
  • 15
  • 9
  • 3
  • 1
  • 1
Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human LOXL1 (NP_005567.2).

    Isotype

    IgG
  • Application Notes

    IF 1:50-1:200

    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

    LOXL1 (Lysyl Oxidase-Like 1 (LOXL1))

    Alternative Name

    LOXL1

    Background

    This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome.

    Molecular Weight

    Observed_MW: 80kDa

    Calculated_MW: 63kDa

    Gene ID

    4016

    UniProt

    Q08397
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