This is a Validated Antibody Database (VAD) review about bovine PDIA2, based on 7 published articles (read how Labome selects the articles), using PDIA2 antibody in all methods. It is aimed to help Labome visitors find the most suited PDIA2 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
Novus Biologicals
domestic rabbit polyclonal
  • western blot; human; loading ...; fig 2c
Novus Biologicals PDIA2 antibody (Novus, NB100-1921) was used in western blot on human samples (fig 2c). Sci Adv (2019) ncbi
mouse monoclonal (RL90)
  • flow cytometry; human; fig 1b
  • immunocytochemistry; human; fig 1d
In order to evaluate the myogenic potential and proliferative capacity of human alveolar mucosa cells, Novus Biologicals PDIA2 antibody (Novus, NB300-517) was used in flow cytometry on human samples (fig 1b) and in immunocytochemistry on human samples (fig 1d). Cell Cycle (2017) ncbi
mouse monoclonal (RL90)
  • western blot; African green monkey; 1:2000; loading ...; fig 2k
In order to characterize two patients with very low plasma triglyceride and apolipoprotein B levels with plasma lipid profiles similar to patients with abetalipoproteinemia, Novus Biologicals PDIA2 antibody (Novus Biologicals, NB300-517) was used in western blot on African green monkey samples at 1:2000 (fig 2k). Biochim Biophys Acta (2016) ncbi
Abcam
domestic rabbit polyclonal
  • immunohistochemistry; human; loading ...; fig 3a
Abcam PDIA2 antibody (Abcam, ab3672) was used in immunohistochemistry on human samples (fig 3a). Autophagy (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; African green monkey; 1:250; loading ...; fig 2j
In order to characterize two patients with very low plasma triglyceride and apolipoprotein B levels with plasma lipid profiles similar to patients with abetalipoproteinemia, Abcam PDIA2 antibody (Abcam, #3672) was used in immunohistochemistry on African green monkey samples at 1:250 (fig 2j). Biochim Biophys Acta (2016) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; 1:500; fig 4
In order to study the cause of a golgi homeostasis disorder with abnormal protein glycosylation due to CCDC115 deficiency, Abcam PDIA2 antibody (Abcam, ab3672) was used in immunocytochemistry on human samples at 1:500 (fig 4). Am J Hum Genet (2016) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; 1:500; fig 4
Abcam PDIA2 antibody (Abcam, ab3672) was used in immunocytochemistry on human samples at 1:500 (fig 4). Am J Hum Genet (2016) ncbi
Abnova
domestic rabbit polyclonal
  • western blot; mouse; fig s2e
Abnova PDIA2 antibody (Abnova, PAB12587) was used in western blot on mouse samples (fig s2e). Cell (2018) ncbi
Articles Reviewed
  1. Oleinik N, Kim J, Roth B, Selvam S, Gooz M, Johnson R, et al. Mitochondrial protein import is regulated by p17/PERMIT to mediate lipid metabolism and cellular stress. Sci Adv. 2019;5:eaax1978 pubmed publisher
  2. Dias D, Kim H, Holl D, Werne Solnestam B, Lundeberg J, Carlen M, et al. Reducing Pericyte-Derived Scarring Promotes Recovery after Spinal Cord Injury. Cell. 2018;173:153-165.e22 pubmed publisher
  3. Zorin V, Pulin A, Eremin I, Korsakov I, Zorina A, Khromova N, et al. Myogenic potential of human alveolar mucosa derived cells. Cell Cycle. 2017;16:545-555 pubmed publisher
  4. Hernandez Tiedra S, Fabrias G, Davila D, Salanueva I, Casas J, Montes L, et al. Dihydroceramide accumulation mediates cytotoxic autophagy of cancer cells via autolysosome destabilization. Autophagy. 2016;12:2213-2229 pubmed
  5. Walsh M, Di Leo E, Okur I, Tarugi P, Hussain M. Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects. Biochim Biophys Acta. 2016;1861:1623-1633 pubmed publisher
  6. Jansen J, Cirak S, van Scherpenzeel M, Timal S, Reunert J, Rust S, et al. CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation. Am J Hum Genet. 2016;98:310-21 pubmed publisher
  7. Jansen J, Timal S, van Scherpenzeel M, Michelakakis H, Vicogne D, Ashikov A, et al. TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation. Am J Hum Genet. 2016;98:322-30 pubmed publisher