OLIG2 anticorps (AA 152-180)

N° du produit ABIN1537886

L’anticorps Lapin Polyclonal anti-OLIG2 a été validé pour WB. Il convient pour détecter OLIG2 dans des échantillons de Souris.

Aperçu rapide pour OLIG2 anticorps (AA 152-180) (ABIN1537886)

Antigène: OLIG2 (Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OLIG2 est non-conjugé

Application: Western Blotting (WB)

Clone: RB39545

Détail du produit anti-OLIG2 anticorps

Épitope: AA 152-180

Homologie: C

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

Immunogène: This OLIG2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 152-180 amino acids from the Central region of human OLIG2.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

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: OLIG2 Antibody (Center) 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

Détails sur OLIG2

Antigène: OLIG2 (Oligodendrocyte Lineage Transcription Factor 2 (OLIG2))

Autre désignation: OLIG2

Sujet: This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14,21)(q11.2,q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome. [provided by RefSeq].

Poids moléculaire: 32385

ID gène: 10215

NCBI Accession: NP_005797

UniProt: Q13516