MNX1 Antikörper (AA 260-340)

Produktnummer ABIN7229710

Dieser Anti-MNX1 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von MNX1 in WB und ELISA. Geeignet für 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: MNX1 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of MNX1 protein

Aufreinigung: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Kommentare:

Primary Antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: 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.

Details zu MNX1

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

Andere Bezeichnung: MNX1

Hintergrund: 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

Molekulargewicht: observerd band 44kDa

Gen-ID: 3110

UniProt: P50219