Use your antibodies-online credentials, if available.
The protein encoded by TSPYL1 is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome.
Showing 10 out of 41 products:
Human Polyclonal TSPYL1 Primary Antibody for WB - ABIN1881952
Vinci, Brauner, Tar, Rouba, Sheth, Sheth, Ravel, McElreavey, Bashamboo: Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility. in Fertility and sterility 2009
Show all 5 Pubmed References
Human Polyclonal TSPYL1 Primary Antibody for ICC, IF - ABIN4363221
Stadler, Rexhepaj, Singan, Murphy, Pepperkok, Uhlén, Simpson, Lundberg: Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells. in Nature methods 2013
Results show that mutations and polymorphisms in the TSPYL1 gene were not associated with sudden infant death syndrome in a cohort of 165 deceased Swiss infants.
Mutations in the TSPYL1 gene do not seem to play a major role in the pathogenesis of idiopathic male infertility, and mutation screening of the TSPYL1 gene can currently not be recommended in routine diagnostics of idiopathic male infertility.
The chromatin remodeling factor (显示 ASH1L 抗体) TSPYL1 had a very similar pattern of expression with an incremental increase in HPFH and decreased expression in deltabeta-thalassemia.
Mutations in TSPYL1 may contribute to anomalies of testicular development/function.
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT).
, TSPY-like protein 1
, testis-specific Y-encoded-like protein 1
, testis-specific-like protein, Y encoded