MLXIPL anticorps (C-Term)

N° du produit ABIN656493

Cet anticorps anti-MLXIPL Polyclonal Lapin (Clone RB31107) (ABIN656493) détecte spécifiquement MLXIPL dans WB et IHC (p). L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour MLXIPL anticorps (C-Term) (ABIN656493)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MLXIPL est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB31107

Détail du produit anti-MLXIPL anticorps

Épitope: AA 624-653, C-Term

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

Immunogène: This MLXIPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 624-653 amino acids from the C-terminal region of human MLXIPL.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:2000. WB: 1:2000. IHC-P: 1:10~50

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: MLXIPL Antibody (C-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

Détails sur MLXIPL

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

Autre désignation: MLXIPL

Sujet: 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.

Poids moléculaire: 93073

ID gène: 51085

NCBI Accession: NP_116569, NP_116570, NP_116571, NP_116572

UniProt: Q9NP71

Pathways: Carbohydrate Homeostasis, Regulation of Carbohydrate Metabolic Process