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MNX1 anticorps (AA 242-271)

Cet anticorps anti-MNX1 est un anticorps Lapin Polyclonal détectant MNX1 dans WB. Adapté pour Humain et Souris.
N° du produit ABIN5535259

Aperçu rapide pour MNX1 anticorps (AA 242-271) (ABIN5535259)

Antigène

Voir toutes MNX1 Anticorps
MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

Reactivité

  • 55
  • 31
  • 30
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 60
Lapin

Clonalité

  • 57
  • 3
Polyclonal

Conjugué

  • 25
  • 5
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MNX1 est non-conjugé

Application

  • 45
  • 23
  • 14
  • 6
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 16
    • 7
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 242-271

    Purification

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

    Immunogène

    This MNX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 242-271 amino acids from the Central region of human MNX1.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

    Autre désignation

    MNX1

    Sujet

    This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].

    Poids moléculaire

    41 kDa

    ID gène

    3110

    UniProt

    P50219
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