Neurogenin 3 anticorps (N-Term)

N° du produit ABIN357411

Cet anticorps anti-Neurogenin 3 est un anticorps Lapin Polyclonal détectant Neurogenin 3 dans WB et EIA. Adapté pour Humain et Souris.

Aperçu rapide pour Neurogenin 3 anticorps (N-Term) (ABIN357411)

Antigène: Neurogenin 3 (NEUROG3)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Neurogenin 3 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-Neurogenin 3 anticorps

Épitope: N-Term

Specificité: This antibody detects Neurogenin3 at N-term.

Purification: Protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS

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

Isotype: Ig Fraction

Information d'application

Indications d'application: ELISA 1: 1,000. Western blot 1: 100 - 1: 500.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: 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 repeated freezing and thawing.

Stock: 4 °C/-20 °C

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

Détails sur Neurogenin 3

Antigène: Neurogenin 3 (NEUROG3)

Autre désignation: Neurogenin-3

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.Synonyms: ATOH5, BHLHA7, Class A basic helix-loop-helix protein 7, NEUROG3, NGN-3, NGN3, Protein atonal homolog 5

Poids moléculaire: 22968 Da

ID gène: 50674, 9606

UniProt: Q5VVI0