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Rabbit anti-PAX3 polyclonal antibody - N-terminal region

Catalog Number:OM105805
OM105805
Discount Price
OM105805-100ul
1~2 Week
100ul
OM105805-50ul
50ul
OM105805-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-PAX3 polyclonal antibody - N-terminal region
Antibody Type Primary Antibodies
Antigen Alias CDHS, HUP2, MGC120381, MGC120382, MGC120383, MGC120384, MGC134778, WS1, WS3
Immunogen The immunogen for anti-PAX3 antibody: synthetic peptide directed towards the N terminal of human PAX3
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity BovineDogGuinea PigHorseHumanMousePigRabbitRat
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol PAX3
Gene Synonyms CDHS
HUP2
MGC120381
MGC120382
MGC120383
MGC120384
MGC134778
WS1
WS3
Gene Full Name Paired box 3
Gene Summary PAX3 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.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.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.
Alternative Names CDHS
HUP2
MGC120381
MGC120382
MGC120383
MGC120384
MGC134778
WS1
WS3
Molecular Weight(MW) 53kDa
Sequence 484 amino acids
Database Links
Entrez Gene 5077
SwissProt ID Q494Z3
Protein Accession NP_852123
Application

Immunoblot

Lane1: 20ug RH30 lysateLane2: 20ug RH30 lysateLane3: 20ug RH41 lysateLane4: 20ug RH41 lysatePrimary Antibody Dilution: 1:1000Secondary Antibody: Donkey anti-rabbit HRPSecondary Antibody Dilution: 1:4000Gene Name: PAX3Submitted by: Dr Joanna Selfe, Institute of Cancer Research
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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