MNX1 抗体
(Motor Neuron and Pancreas Homeobox 1 (MNX1))
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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62 results
MNX1
适用: 人, 大鼠
WB, ELISA, FACS, IHC (p), IHC (fro)
宿主: 兔
Polyclonal
unconjugated
1 image
Rockland Original
Latest Publications for our MNX1 抗体
: "Persistent expression of Hlxb9 in the pancreatic epithelium impairs pancreatic development." in: Developmental biology, Vol. 240, Issue 1, pp. 247-53, (2002) (PubMed).Aliases for MNX1 抗体
motor neuron and pancreas homeobox 1 (MNX1) 抗体motor neuron homeobox transcription factor (mnx1) 抗体
motor neuron and pancreas homeobox 1 (Mnx1) 抗体
motor neuron and pancreas homeobox 1 (mnx1) 抗体
HB9 抗体
HLXB9 抗体
Hlxb9 抗体
hlxb9 抗体
HOXHB9 抗体
MNR2 抗体
SCRA1 抗体
zgc:112174 抗体
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