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PWP2 Antibody (D-20): sc-83743

 |  Datasheet

(Based on data analysis)

  • PWP2 Antibody (D-20) is a rabbit polyclonal IgG provided at 100 µg/ml
  • epitope mapping within an internal region of PWP2 of human origin
  • recommended for detection of PWP2 of mouse, rat and human origin by WB, IF and ELISA; non cross-reactive with other PWP family members; also reactive with additional species, including bovine and porcine
  • blocking peptide, sc-83743 P

See additional PWP Antibodies including PWP, PWP1 and PWP2.

Ordering InformationGene Info
Recommended Support Products:
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WB   IF   siRNA  
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 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
PWP2 Antibody (D-20) sc-83743 100 µg/ml $279
PWP2 (D-20) P sc-83743 P
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
PWP2 siRNA (h) sc-91396 10 µM $258
PWP2 siRNA (m) sc-152598 10 µM $258
PWP2 (h)-PR sc-91396-PR 10 µM, 20 µl $23
PWP2 (m)-PR sc-152598-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
PWP2 shRNA Plasmid (h) sc-91396-SH 20 µg $520
PWP2 shRNA Plasmid (m) sc-152598-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
PWP2 shRNA (h) Lentiviral Particles sc-91396-V 200 µl $625
PWP2 shRNA (m) Lentiviral Particles sc-152598-V 200 µl $625
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human PWP2 5822 21q22.3 Q15269

PWP2 (periodic tryptophan protein 2), also known as EHOC-17, is a 919 amino acid protein that is the human homolog of the Saccharomyces cerevisiae periodic Trp 2 protein. Belonging to the WD repeat PWP2 family of proteins, PWP2 contains 14 WD repeats and has over 40% identity to the yeast homolog. PWP2 is localized to the nucleus and is implicated to play a role in early G1 phase of the cell cycle. Essential for cell viability, PWP2 is also thought to be a candidate for various genetic disorders, such as progressive myoclonus epilepsy (EPM1), autoimmune polyglandular disease (APECED) and holoprosencephaly-1 (HPE1). The PWP2 gene maps to chromosome 21q22.3.