MLXIPL anticorps (MLX Interacting Protein-Like) (AA 623-653)

N° du produit ABIN953464

Détail du produit anti-MLXIPL anticorps

Antigène:

MLXIPL

Épitope: AA 623-653, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MLXIPL est non-conjugé

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

Specificité: This antibody recognizes Human MLXIPL (C-term).

Purification: Protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 623-653 amino acids from the C-terminal region of human MLXIPL

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur MLXIPL

Antigène:

MLXIPL

Autre désignation: MLXIPL (MLXIPL Antibody Extrait)

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.Synonyms: MIO, MLX-interacting protein-like, WBSCR14, WS basic-helix-loop-helix leucine zipper protein, Williams-Beuren syndrome chromosomal region 14 protein

Poids moléculaire: 93073 Da

ID gène: 51085

NCBI Accession: NP_116569

Pathways: Carbohydrate Homeostasis, Regulation of Carbohydrate Metabolic Process