MNX1 Polyclonal Antibody

SKU: BT-AP11418

Size:100μL

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.

Research_area:Developmental biology; Epigenetics and nuclear signaling; Neuroscience; Stem cells

Target_protein:MNX1

applications:WB, ELISA

Reactivity:Human, Mouse

Clonality:Polyclonal

Clone ID:

Host:Rabbit

Isotype:IgG

Gene Symbol/ Name:Motor neuron and pancreas homeobox protein 1

Immunogen:The antiserum was produced against synthesized peptide derived from human AMPK alpha around the phosphorylation site of Thr172. AA range:140-189

Storage:-20°C for 1 year

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Concentration:1 mg/ml

Molecular weight(Da):

UniProt accession:Human: P50219; Mouse: Q9QZW9

Synonyms:Motor neuron and pancreas homeobox protein 1 ;Homeobox protein HB9

GeneID:Human: 3110