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Rabbit anti-Human LOXL1 Monoclonal Antibody

The antibody against LOXL1 was raised in Rabbit using the recombinant protein of human LOXL1 as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-15102A

The antibody against LOXL1 was raised in Rabbit using the recombinant protein of human LOXL1 as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-15102A ClonalityMonoclonal
Host SpeciesRabbitTarget NameLoxl1
Target SynonymsLOL; LOXL; LOXL1FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive SamplesU-87MGApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant protein of human LOXL1.Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ08397
Background Information
  • Uniprot Id

    Q08397

  • Target Species

    Human

  • Target Name

    LOXL1

  • Target Full Name

    Lysyl oxidase homolog 1

  • Target Function

    Active on elastin and collagen substrates.

  • Target Involvement

    Exfoliation syndrome (XFS)

  • Target Subcellular Location

    Secreted, extracellular space.

  • Target Protein Families

    Lysyl oxidase family

  • Target Tissue Specificity

    Expressed in ocular tissues including the iris, ciliary body, lens and optic nerve. Not detected in the retina.

  • Target Research Area

    Cell Biology, Metabolism

  • Target Synonyms

    LOXL1; LOXLLysyl oxidase homolog 1; EC 1.4.3.-; Lysyl oxidase-like protein 1; LOL

  • Target 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.

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