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GEMIN6 anticorps (AA 21-120) (FITC)

Cet anticorps Lapin Polyclonal détecte spécifiquement GEMIN6 dans WB, IF (cc) et IF (p). Il présente une réactivité envers Humain et Rat.
N° du produit ABIN1709515

Aperçu rapide pour GEMIN6 anticorps (AA 21-120) (FITC) (ABIN1709515)

Antigène

Voir toutes GEMIN6 Anticorps
GEMIN6 (Gem (Nuclear Organelle) Associated Protein 6 (GEMIN6))

Reactivité

  • 29
  • 16
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Rat

Hôte

  • 25
  • 4
Lapin

Clonalité

  • 27
  • 2
Polyclonal

Conjugué

  • 12
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GEMIN6 est conjugé à/à la FITC

Application

  • 24
  • 12
  • 12
  • 10
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Épitope

    • 14
    • 9
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 21-120

     Réactivité croisée

    Humain, Rat

    Homologie

    Mouse,Horse,Rabbit

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human Gemin 6

    Isotype

    IgG
  • Indications d'application

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Date de péremption

    12 months
  • Antigène

    GEMIN6 (Gem (Nuclear Organelle) Associated Protein 6 (GEMIN6))

    Autre désignation

    Gemin 6

    Sujet

    Synonyms: FLJ23459, Gemin6, Gemin-6, Gem nuclear organelle associated protein 6, Gem-associated protein 6, GEMI6, GEMI6_HUMAN, Gemin-6, GEMIN6, SIP2.

    Background: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (Survival of Motor Neuron) gene. Gemin6, the protein product of human chromosome 2p22.2, associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin3, Gemin4 and Gemin5 as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. The SMN complex is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (Gemini of the coiled bodies).

    ID gène

    79833

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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