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ATL1 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-ATL1 a été validé pour WB. Il convient pour détecter ATL1 dans des échantillons de Humain.
N° du produit ABIN1537385

Aperçu rapide pour ATL1 anticorps (C-Term) (ABIN1537385)

Antigène

Voir toutes ATL1 Anticorps
ATL1 (Atlastin GTPase 1 (ATL1))

Reactivité

  • 31
  • 19
  • 19
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 43
  • 3
Lapin

Clonalité

  • 43
  • 3
Polyclonal

Conjugué

  • 17
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ATL1 est non-conjugé

Application

  • 34
  • 19
  • 13
  • 13
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB36288
  • Épitope

    • 15
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 477-504, C-Term

    Homologie

    B, Pr, M, Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This ATL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 477-504 amino acids from the C-terminal region of human ATL1.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Stockage commentaire

    ATL1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    ATL1 (Atlastin GTPase 1 (ATL1))

    Autre désignation

    ATL1

    Sujet

    The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene.

    Poids moléculaire

    63544

    ID gène

    51062

    NCBI Accession

    NP_001121185, NP_056999, NP_853629

    UniProt

    Q8WXF7
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