Neurogenin 3 anticorps (N-Term)

N° du produit ABIN388770

Cet anticorps anti-Neurogenin 3 est un anticorps Lapin Polyclonal détectant Neurogenin 3 dans WB, IF et IHC (p). Adapté pour Humain et Souris.

Aperçu rapide pour Neurogenin 3 anticorps (N-Term) (ABIN388770)

Antigène: Neurogenin 3 (NEUROG3)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Neurogenin 3 est non-conjugé

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

Clone: RB02913

Détail du produit anti-Neurogenin 3 anticorps

Épitope: AA 40-69, N-Term

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

Immunogène: This Neurogenin3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 40-69 amino acids from the N-terminal region of human Neurogenin3.

Isotype: IgG

Information d'application

Indications d'application: IF: 1:10~50. WB: 1:2000. WB: 1:500. WB: 1:2000. IHC-P: 1:25. IHC-P: 1:25

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.

Conseil sur la manipulation: Avoid freeze-thaw cycles.

Stock: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots.

Date de péremption: 6 months

Détails sur Neurogenin 3

Antigène: Neurogenin 3 (NEUROG3)

Autre désignation: Neurogenin3

Sujet: Neurogenin-3 belongs to a family of basic helix-loop-helix transcription factors involved in the determination of neural precursor cells in the neuroectoderm. Neurogenin-3 also required for the specification of a common precursor of the 4 pancreatic endocrine cell types. Defects in NEUROG3 are the cause of congenital malabsorptive diarrhea 4 (DIAR4). DIAR4 is an autosomal recessive disorder characterized by generalized malabsorption and a paucity of enteroendocrine cells.

Poids moléculaire: 23077

ID gène: 50674

NCBI Accession: NP_066279

UniProt: Q9Y4Z2