Product Browser
 
Product Compare
 
  • Click this icon to add products to compare list. Select up to 10 products.
  • Choose your location
Integrated Solutions & Services
BULK
100% Guarantee_July
ISO

PAX3 Pre-design Chimera RNAi   

  • Catalog # : H00005077-R07
  • Visit Frequency :
  • Current Country :
  • Size
  • Price
  • In Stock
  • Availability
  • Cart
  • 10 nmol
  • USD $ 239
  • Stock Image
  • order now, ship in 2 weeks
  • Add to Cart
  • 20 nmol
  • USD $ 289
  • Stock Image
  • order now, ship in 2 weeks
  • Add to Cart
  • Payment Information

    Credit card :
    or Purchase Order Number

  • Email : sales@abnova.com
    Phone : +1-909-992-0619 (new)
    Fax : +1-909-992-3401
  • Products will be shipped directly to the customer.
  • Product Compare
  • Save To Interest Product
  • Add Review
  • Print
  • PDF Download
  • Specification
  • Product Description:
  • Homo sapiens paired box gene 3 (Waardenburg syndrome 1) (PAX3), transcript variant PAX3G, mRNA.
  • Reactivity:
  • Human
  • Supplied Product:
  • DEPC water
  • Target Refseq:
  • NM_181461
  • Target Region:
  • Coding sequence
  • Storage Instruction:
  • Store at -20°C, do not exceed 4 - 5 freeze-thaw cycles to ensure product integrity.
  • Note:
  • Position of the Chimera RNAi.
    The related RNAi products listed below were designed from different accesion number but sharing the same RNAi sequence.

  • Publication Reference
  • Applications
  • RNAi Knockdown
  • Application Image
  • RNAi Knockdown
  • Gene Information
  • Entrez GeneID:
  • 5077
  • Gene Name:
  • PAX3
  • Gene Alias:
  • CDHS,HUP2,MGC120381,MGC120382,MGC120383,MGC120384,MGC134778,WS1
  • Gene Description:
  • paired box 3
  • Gene Summary:
  • 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
  • Other Designations:
  • paired box homeotic gene 3,paired domain gene 3,paired domain gene HuP2
    If you have a question or comment, please select the topic you would like to contact.

Your message has been sent successfully!