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PAX3
Paired box 3HUP2, WS1
This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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| Invitrogen Antibodies |  38-1801 |
10 references | Polyclonal |
WB
ICC
IP
IHC
FC
OA
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| Novus Biologicals | NB100-1420 |
3 references | Polyclonal |
WB
EL
IP
IHC
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| antibodies-online | ABIN250216 |
2 references | Polyclonal |
WB
EL
ICC
IHC
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| GeneTex | GTX100663 |
1 references | Polyclonal |
WB
ICC
IHC
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| R&D Systems | MAB2457 |
9 references | Monoclonal |
WB
ICC
FC
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