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SIM1 anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-SIM1 a été validé pour WB. Il convient pour détecter SIM1 dans des échantillons de Poisson zèbre (Danio rerio).
N° du produit ABIN6244173

Aperçu rapide pour SIM1 anticorps (N-Term) (ABIN6244173)

Antigène

Voir toutes SIM1 Anticorps
SIM1 (Single-Minded Homolog 1 (SIM1))

Reactivité

  • 19
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Poisson zèbre (Danio rerio)

Hôte

  • 18
  • 1
Lapin

Clonalité

  • 19
Polyclonal

Conjugué

  • 11
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp SIM1 est non-conjugé

Application

  • 13
  • 11
  • 11
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB32160
  • Épitope

    • 10
    • 4
    • 4
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Homologie

    M, D

    Purification

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

    Immunogène

    This Zebrafish SIM1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of Zebrafish SIM1.

    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

    Date de péremption

    6 months
  • Antigène

    SIM1 (Single-Minded Homolog 1 (SIM1))

    Autre désignation

    SIM1

    Sujet

    SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.

    Poids moléculaire

    82919

    UniProt

    F1QMF7
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