MLXIPL anticorps

N° du produit ABIN6571243

Cet anticorps anti-MLXIPL est un anticorps Lapin Polyclonal détectant MLXIPL dans WB. Adapté pour Humain, Rat et Souris.

Aperçu rapide pour MLXIPL anticorps (ABIN6571243)

Antigène: MLXIPL (MLX Interacting Protein-Like (MLXIPL))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MLXIPL est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-MLXIPL anticorps

Purification: Affinity purification

Immunogène: Recombinant protein of human MLXIPL

Isotype: IgG

Information d'application

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

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: 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 MLXIPL

Antigène: MLXIPL (MLX Interacting Protein-Like (MLXIPL))

Autre désignation: MLXIPL

Sujet:

Synonyms: carbohydrate response element binding protein,bHLHd14,Carbohydrate responsive element binding protein,Class D basic helix-loop-helix protein 14,MIO,MLX interacting protein like,Mlx interactor,MLX-interacting protein-like,MLXIPL,MONDOB,WBS14,WBSCR 14,WBSCR14,Williams Beuren syndrome chromosome region 14,Williams Beuren syndrome chromosome region 14 protein,Williams-Beuren syndrome chromosomal region 14 protein,WS basic helix loop helix leucine zipper protein,WS basic-helix-loop-helix leucine zipper protein,WS bHLH,WS-bHLH

Background: This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants.

Poids moléculaire:

Observed_MW: 93kDa

Calculated_MW: 62kDa/78kDa/90kDa/92kDa/93kDa

ID gène: 51085

UniProt: Q9NP71

Pathways: Carbohydrate Homeostasis, Regulation of Carbohydrate Metabolic Process