MNX1 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP16474c
Background:
This gene encodes a nuclear protein, which contains ahomeobox domain and is a transcription factor. Mutations in thisgene result in Currarino syndrome, an autosomic dominant congenitalmalformation. Alternatively spliced transcript variants encodingdifferent isoforms have been found for this gene. [provided byRefSeq].
Other Names:
Motor neuron and pancreas homeobox protein 1, Homeobox protein HB9, MNX1, HLXB9
Gene Name: MNX1
Gene ID: 3110
Primary Accession: P50219
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a nuclear protein, which contains ahomeobox domain and is a transcription factor. Mutations in thisgene result in Currarino syndrome, an autosomic dominant congenitalmalformation. Alternatively spliced transcript variants encodingdifferent isoforms have been found for this gene. [provided byRefSeq].
Other Names:
Motor neuron and pancreas homeobox protein 1, Homeobox protein HB9, MNX1, HLXB9
Gene Name: MNX1
Gene ID: 3110
Primary Accession: P50219
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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