MNX1 Polyclonal Antibody
Product Specifications
Background
Motor neuron and pancreas homeobox 1 (MNX1) Homo sapiens 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]
Gene ID
3110
Swiss Prot
P50219
Cross Reactivity
Human; Mouse
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Buffer
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Molecular Weight
44
Storage Conditions
-20°C/1 year
Protein Weight
44
Available Sizes
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