MNX1 Antikörper (AA 260-340)

Produktnummer ABIN7229710

Der Kaninchen Polyklonal anti-MNX1 Antikörper (ABIN7229710) detektiert spezifisch MNX1 in WB und ELISA. Dieser Antikörper reagiert spezifisch mit Proben aus Human und Maus.

Kurzübersicht für MNX1 Antikörper (AA 260-340) (ABIN7229710)

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MNX1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-MNX1 Antikörper

Bindungsspezifität: AA 260-340

Verwendungszweck: Rabbit Anti-MNX1 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of MNX1 protein

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 12 months

Details zu MNX1

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

Andere Bezeichnung: MNX1

Hintergrund: Motor neuron and pancreas homeobox protein 1, Homeobox protein HB9MNX1 (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.

Molekulargewicht: 44kD

Gen-ID: 3110

UniProt: P50219