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LAMA3 anticorps

Cet anticorps anti-LAMA3 est un anticorps Lapin Polyclonal détectant LAMA3 dans ELISA et IHC. Adapté pour Humain et Souris.
N° du produit ABIN7002526

Aperçu rapide pour LAMA3 anticorps (ABIN7002526)

Antigène

Voir toutes LAMA3 Anticorps
LAMA3 (Laminin, alpha 3 (LAMA3))

Reactivité

  • 36
  • 14
  • 14
Humain, Souris

Hôte

  • 31
  • 4
  • 1
Lapin

Clonalité

  • 32
  • 4
Polyclonal

Conjugué

  • 12
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp LAMA3 est non-conjugé

Application

  • 13
  • 12
  • 7
  • 6
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Synthetic peptide of human LAMA3

    Isotype

    IgG
  • Indications d'application

    IHC 1:25-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.4 mg/mL

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

    LAMA3 (Laminin, alpha 3 (LAMA3))

    Autre désignation

    LAMA3

    Sujet

    Laminins are basement membrane components thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. The protein encoded by this gene is the alpha-3 subunit of laminin 5, which is a complex glycoprotein composed of three subunits (alpha, beta, and gamma). Laminin 5 is thought to be involved in cell adhesion, signal transduction and differentiation of keratinocytes. Mutations in this gene have been identified as the cause of Herlitz type junctional epidermolysis bullosa. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.

    NCBI Accession

    NP_000218

    UniProt

    Q16787
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