MNX1 antibody (AA 260-340)

Catalog No. ABIN7229710

The Rabbit Polyclonal anti-MNX1 antibody (ABIN7229710) specifically detects MNX1 in WB and ELISA. The antibody is reactive with Human and Mouse samples.

Quick Overview for MNX1 antibody (AA 260-340) (ABIN7229710)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MNX1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-MNX1 Antibody

Binding Specificity: AA 260-340

Purpose: Rabbit Anti-MNX1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of MNX1 protein

Purification: 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

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: 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.

Expiry Date: 12 months

Target Details for MNX1

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

Alternative Name: MNX1

Background: 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.

Molecular Weight: 44kD

Gene ID: 3110

UniProt: P50219