TBL1X anticorps (AA 100-200)

N° du produit ABIN7270901

L’anticorps Lapin Polyclonal anti-TBL1X a été validé pour WB. Il convient pour détecter TBL1X dans des échantillons de Humain.

Aperçu rapide pour TBL1X anticorps (AA 100-200) (ABIN7270901)

Antigène: TBL1X (Transducin (Beta)-Like 1X-Linked (TBL1X))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TBL1X est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-TBL1X anticorps

Épitope: AA 100-200

Fonction: TBL1X Rabbit pAb

Séquence: LISILQKGLQ YVEAEISINE DGTVFDGRPI ESLSLIDAVM PDVVQTRQQA FREKLAQQQA SAAAAAAAAT AAATAATTTS AGVSHQNPSK NREATVNGEE N

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: A synthetic peptide corresponding to a sequence within amino acids 100-200 of human TBL1X (NP_005638.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur TBL1X

Antigène: TBL1X (Transducin (Beta)-Like 1X-Linked (TBL1X))

Autre désignation: TBL1X

Sujet: The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene.,TBL1X,EBI,SMAP55,TBL1,Epigenetics & Nuclear Signaling,Nuclear Receptor Signaling,Cancer,Endocrine & Metabolism,Lipid Metabolism,Endocrine and metabolic diseases,Diabetes,Metabolic disorders,Obesity,Neuroscience,TBL1X

Poids moléculaire: 57kDa/62kDa

ID gène: 6907

UniProt: O60907

Pathways: Sensory Perception of Sound, Regulation of Lipid Metabolism by PPARalpha