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KIF1A anticorps (AA 1079-1628)

L’anticorps anti-KIF1A Polyclonal Lapin est utilisé pour la détection de KIF1A dans des échantillons de Souris, Humain et Rat. Il a été validé pour ELISA, WB et FACS.
N° du produit ABIN7870017
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour KIF1A anticorps (AA 1079-1628) (ABIN7870017)

Antigène

Voir toutes KIF1A Anticorps
KIF1A (Kinesin Family Member 1A (KIF1A))

Reactivité

  • 10
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Souris, Humain, Rat

Hôte

  • 10
  • 2
Lapin

Clonalité

  • 10
  • 2
Polyclonal

Conjugué

  • 8
  • 2
  • 1
  • 1
Cet anticorp KIF1A est non-conjugé

Application

  • 7
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS)
  • Épitope

    • 5
    • 2
    • 1
    • 1
    • 1
    AA 1079-1628

    Fonction

    KIF1A Antibody

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids H1079-Y1628) was used as the immunogen for the KIF1A antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the KIF1A antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the KIF1A antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    KIF1A (Kinesin Family Member 1A (KIF1A))

    Autre désignation

    KIF1A

    Sujet

    Kinesin-like protein KIF1A, also known as axonal transporter of synaptic vesicles or microtubule-based motor KIF1A, is a protein that in humans is encoded by the KIF1A gene. The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described.

    UniProt

    Q12756
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