PAX3 Primary Antibody
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.
Ascitic fluid containing 0.03% sodium azide.
4°C; -20°C for long term storage
Figure 1: Western blot analysis using PAX3 mAb against human PAX3 recombinant protein. (Expected MW is 32.6 kDa)
Figure 2: Western blot analysis using PAX3 mAb against HEK293 (1) and PAX3 (AA: 142-203)-hIgGFc transfected HEK293 (2) cell lysate.
Figure 3: Western blot analysis using PAX3 mouse mAb against A549 (1), A431 (2), Jurkat (3), Rat spleen (4) and Mouse liver (5) cell lysate.
Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng);
For Research Use Only. Not for use in diagnostic procedures.