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PTPN13LY Antibody (S-14): sc-79704

 |  Datasheet

(Based on data analysis)

  • PTPN13LY Antibody (S-14) is a rabbit polyclonal IgG provided at 100 µg/ml
  • epitope mapping within an internal region of PTPN13LY of human origin
  • recommended for detection of PTPN13LY of human origin by WB, IF and ELISA
  • blocking peptide, sc-79704 P
 

See additional PTPN Antibodies including PTPN, PTPN20, PTPN13LY, PTPN20A , PTPN20B and PTPN21.

Ordering InformationGene Info
Recommended Support Products:
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WB   IF   siRNA  
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 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
PTPN13LY Antibody (S-14) sc-79704 100 µg/ml $279
PTPN13LY (S-14) P sc-79704 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
PTPN13LY siRNA (h) sc-76289 10 µM $258
PTPN13LY (h)-PR sc-76289-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
PTPN13LY shRNA Plasmid (h) sc-76289-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
PTPN13LY shRNA (h) Lentiviral Particles sc-76289-V 200 µl $625
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human PRY 9081 Yq11.223 O14603
400019
 


The protein tyrosine phosphatase (PTP) family of proteins are signaling molecules that regulate processes such as cell growth, cell differentiation, oncogenic transformation and the mitotic cycle. PTPN13LY (PTPN13-like, Y-linked), also known as PRY, PTPN13LY2 or PRY2, is a 147 amino acid protein that localizes to the testis and may function in a similar manner to PTP proteins. The gene encoding PTPN13LY maps to human chromosome Y and is expressed as two alternatively spliced isoforms. Chromosome Y contains approximately 58 million base pairs and houses over 80 genes, many of which are essential for proper sexual development. The Y chromosome is the human sex determining chromosome, necessary for male development and, while deletions or defects in chromosome Y-encoded genes are not lethal, they may greatly impair masculine development and function.