MNX1

gene product
HB9, HLXB9, HOXHB9, SCRA1
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]
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213 antibodies from 35 providers.

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Antibody
antibodies-online
68 antibodies
Abnova Corporation
2 antibodies
Novus Biologicals
6 antibodies
LifeSpan BioSciences, Inc.
36 antibodies
OriGene
4 antibodies
Acris Antibodies GmbH
2 antibodies
Invitrogen Antibodies
6 antibodies
Rockland Immunochemicals, Inc.
1 antibody
Boster Biological Technology
2 antibodies
Cusabio Biotech Co., Ltd
4 antibodies
Bethyl Laboratories
3 antibodies
NovoPro Bioscience Inc.
2 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Affinity Biosciences
1 antibody
Cell Signaling Technology, Inc
1 antibody
Proteintech Group
1 antibody
Wuhan Fine Biotech Co., Ltd.
1 antibody
Biorbyt
11 antibodies
Aviva Systems Biology
3 antibodies
Abgent
3 antibodies
GeneTex
2 antibodies
RabMAbs
2 antibodies
Arigo
1 antibody
Atlas Antibodies
1 antibody
ProSci
2 antibodies
Creative Biolabs
3 antibodies
EMD Millipore
1 antibody
MyBioSource
1 antibody
St John's Laboratory
1 antibody
United States Biological
13 antibodies
Abbexa
7 antibodies
MilliporeSigma / Merck KGaA
3 antibodies
Creative Diagnostics
1 antibody
Leading Biology
1 antibody