MNX1 rabbit pAb
Ref. EK-ES9821
50µl | 188.00 € | ||
100µl | 316.00 € |
Product Information
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],
Chemical properties
Technical inquiry about: EK-ES9821 MNX1 rabbit pAb
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