This is a Validated Antibody Database (VAD) review about human CWF19L1, based on 1 published articles (read how Labome selects the articles), using CWF19L1 antibody in all methods. It is aimed to help Labome visitors find the most suited CWF19L1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
CWF19L1 synonym: C19L1; SCAR17; hDrn1; CWF19-like protein 1; CWF19-like 1 cell cycle control

Invitrogen
rabbit polyclonal
  • western blot; human; loading ...; fig 3e
In order to study the effect of exome sequencing in regards to CWF19L1 mutation, intellectual disability and cerebellar atrophy, Invitrogen CWF19L1 antibody (Life Technologies, PA5-31646) was used in western blot on human samples (fig 3e). Am J Med Genet A (2016) ncbi
Sigma-Aldrich
rabbit polyclonal
  • western blot; human; loading ...; fig 3e
In order to study the effect of exome sequencing in regards to CWF19L1 mutation, intellectual disability and cerebellar atrophy, Sigma-Aldrich CWF19L1 antibody (Sigma, HPA036890) was used in western blot on human samples (fig 3e). Am J Med Genet A (2016) ncbi
Articles Reviewed
  1. Evers C, Kaufmann L, Seitz A, Paramasivam N, Granzow M, Karch S, et al. Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy. Am J Med Genet A. 2016;170:1502-9 pubmed publisher