This is a Validated Antibody Database (VAD) review about human plakophilin 1, based on 3 published articles (read how Labome selects the articles), using plakophilin 1 antibody in all methods. It is aimed to help Labome visitors find the most suited plakophilin 1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
plakophilin 1 synonym: B6P

Abcam
domestic rabbit monoclonal (EPR14890)
  • immunohistochemistry; human; loading ...; fig 7a
  • western blot; human; loading ...; fig 9b
Abcam plakophilin 1 antibody (Abcam, ab183512) was used in immunohistochemistry on human samples (fig 7a) and in western blot on human samples (fig 9b). Sci Adv (2021) ncbi
Invitrogen
mouse monoclonal (10B2)
  • immunohistochemistry - frozen section; human; loading ...; fig 2e
In order to characterize the first female individuals affected with the ectodermal dysplasia/skin fragility syndrome, Invitrogen plakophilin 1 antibody (Zymed, 10B2) was used in immunohistochemistry - frozen section on human samples (fig 2e). J Invest Dermatol (2004) ncbi
Santa Cruz Biotechnology
mouse monoclonal (10B2)
  • immunohistochemistry - frozen section; human; loading ...
Santa Cruz Biotechnology plakophilin 1 antibody (Santa, 10B2) was used in immunohistochemistry - frozen section on human samples . Hum Mol Genet (2011) ncbi
Articles Reviewed
  1. Li K, Wu R, Zhou M, Tong H, Luo K. Desmosomal proteins of DSC2 and PKP1 promote cancer cells survival and metastasis by increasing cluster formation in circulatory system. Sci Adv. 2021;7:eabg7265 pubmed publisher
  2. Pigors M, Kiritsi D, Krümpelmann S, Wagner N, He Y, Podda M, et al. Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity. Hum Mol Genet. 2011;20:1811-9 pubmed publisher
  3. Sprecher E, Molho Pessach V, Ingber A, Sagi E, Indelman M, Bergman R. Homozygous splice site mutations in PKP1 result in loss of epidermal plakophilin 1 expression and underlie ectodermal dysplasia/skin fragility syndrome in two consanguineous families. J Invest Dermatol. 2004;122:647-51 pubmed