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TBL2 anticorps (N-Term)

Cet anticorps anti-TBL2 est un anticorps Lapin Polyclonal détectant TBL2 dans WB et IHC (p). Adapté pour Humain.
N° du produit ABIN656760

Aperçu rapide pour TBL2 anticorps (N-Term) (ABIN656760)

Antigène

Voir toutes TBL2 Anticorps
TBL2 (Transducin (Beta)-Like 2 (TBL2))

Reactivité

  • 22
  • 4
  • 2
  • 2
  • 2
Humain

Hôte

  • 20
  • 2
Lapin

Clonalité

  • 22
Polyclonal

Conjugué

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TBL2 est non-conjugé

Application

  • 21
  • 11
  • 11
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32541
  • Épitope

    • 7
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 43-72, N-Term

    Purification

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

    Immunogène

    This TBL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-72 amino acids from the N-terminal region of human TBL2.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. IHC-P: 1:10~50

    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

    TBL2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Date de péremption

    6 months
  • Antigène

    TBL2 (Transducin (Beta)-Like 2 (TBL2))

    Autre désignation

    TBL2

    Sujet

    This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

    Poids moléculaire

    49798

    ID gène

    26608

    NCBI Accession

    NP_036585

    UniProt

    Q9Y4P3
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