MNX1 antibody (AA 260-340)

Catalog No. ABIN7229710

This anti-MNX1 antibody is a Rabbit Polyclonal antibody detecting MNX1 in WB and ELISA. Suitable for Human and Mouse.

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: MNX1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of MNX1 protein

Purification: 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

Isotype: IgG

Application Details

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

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: 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.

Target Details for MNX1

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

Alternative Name: MNX1

Background: 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

Molecular Weight: observerd band 44kDa

Gene ID: 3110

UniProt: P50219