MNX1 (NM_005515) Human Recombinant Protein

Product Specifications

Background

This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Overview

Recombinant protein of human motor neuron and pancreas homeobox 1 (MNX1)

Synonyms

HB9; HLXB9; HOXHB9; SCRA1

Gene ID

3110

UniProt

P50219

Accession Number mRNA

NM_005515

Chromosomal Location

7q36.3

Expression System

HEK293T

Tag

C-Myc/DDK

Related Pathways

Maturity onset diabetes of the young

Field of Research

Maturity onset diabetes of the young

Concentration

>50 ug/mL as determined by microplate BCA method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Form

Liquid

Buffer

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Function

Druggable Genome, ES Cell Differentiation/IPS

Molecular Weight

40.4 kDa

Storage Conditions

Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.