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Rabbit anti-Human PAX3 Polyclonal Antibody

The antibody against PAX3 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-236 of human PAX3 (NP_852122.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.

ADA-04547A

The antibody against PAX3 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-236 of human PAX3 (NP_852122.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.

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Specifications


Cat.No ADA-04547A ClonalityPolyclonal
Host SpeciesRabbitTarget NamePAX3
Target SynonymsWS1; WS3; CDHS; HUP2; PAX-3; PAX3FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive Samples293T, Rat testisApplicationELISA, WB, IF/ICC, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-236 of human PAX3 (NP_852122.1).Target SpeciesHuman
Uniprot IDP23760Immunogen Sequence
Background Information
  • Uniprot Id

    P23760

  • Target Species

    Human

  • Target Name

    PAX3

  • Target Full Name

    Paired box protein Pax-3

  • Target Function

    Transcription factor that may regulate cell proliferation, migration and apoptosis. Involved in neural development and myogenesis. Transcriptional activator of MITF, acting synergistically with SOX10.

  • Target Involvement

    Waardenburg syndrome 1 (WS1); Waardenburg syndrome 3 (WS3); Craniofacial-deafness-hand syndrome (CDHS); Rhabdomyosarcoma 2 (RMS2)

  • Target Subcellular Location

    Nucleus.

  • Target Protein Families

    Paired homeobox family

  • Target Synonyms

    CDHS; HUP 2; HUP2; MGC120381; MGC120382; MGC120383; MGC120384; MGC134778; Paired box 3; Paired box gene 3; Paired box homeotic gene 3; Paired box protein Pax 3; Paired box protein Pax-3; Paired box protein Pax3; Paired domain gene 3; Paired domain gene HuP2; PAX 3; Pax3; PAX3/FKHR fusion gene; PAX3_HUMAN; Sp; splotch; Waardenburg syndrome 1; WS 1; WS1; WS3

  • Target Background

    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.

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