Rabbit Polyclonal Antibody to MNX1

Description
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.

Specification
Aliases	HB9; HLXB9; SCRA1; HOXHB9
Swissprot	P50219
WB Predicted band size	41 kDa
Host/Isotype	Rabbit IgG
Antibody Type	Primary antibody
Storage	Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species Reactivity	Human
Immunogen	Synthetic peptide of human MNX1
Formulation	Purified antibody in PBS with 0.05% sodium azide and 50% glycerol.

Application
WB	1/200-1/1000
ELISA	1/5000-1/10000