MNX1 anticorps (AA 260-340)

N° du produit ABIN7229710

Cet anticorps anti-MNX1 Polyclonal Lapin (ABIN7229710) détecte spécifiquement MNX1 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour MNX1 anticorps (AA 260-340) (ABIN7229710)

Antigène: MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MNX1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-MNX1 anticorps

Épitope: AA 260-340

Fonction: MNX1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of MNX1 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human MNX1 protein at AA range: 260-340

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur MNX1

Antigène: MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

Autre désignation: MNX1

Sujet: Rabbit Anti-MNX1 Polyclonal Antibody,Motor neuron and pancreas homeobox protein 1, Homeobox protein HB9,MNX1 (Motor Neuron And Pancreas Homeobox 1) is a Protein Coding gene. Diseases associated with MNX1 include Currarino Syndrome and Meningocele. Among its related pathways are Regulation of beta-cell development and Neural Stem Cell Differentiation Pathways and Lineage-specific Markers. MNX1 encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in MNX1 result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for MNX1.,MNX1

Poids moléculaire: observerd band 44kDa

ID gène: 3110

UniProt: P50219