This is a Validated Antibody Database (VAD) review about human NIPBL, based on 3 published articles (read how Labome selects the articles), using NIPBL antibody in all methods. It is aimed to help Labome visitors find the most suited NIPBL antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
NIPBL synonym: CDLS; CDLS1; IDN3; IDN3-B; Scc2; nipped-B-like protein; Nipped-B homolog; SCC2 homolog; delangin; sister chromatid cohesion 2 homolog

Santa Cruz Biotechnology
mouse monoclonal (C-9)
  • western blot; human; 1:500; loading ...; fig 1b
In order to describe a role for NIPBL in DNA damage repair, Santa Cruz Biotechnology NIPBL antibody (Santa Cruz, sc-374625) was used in western blot on human samples at 1:500 (fig 1b). J Cell Sci (2017) ncbi
mouse monoclonal (C-9)
  • ChIP-Seq; human; fig 4
Santa Cruz Biotechnology NIPBL antibody (Santa Cruz Biotechnology, sc-374625) was used in ChIP-Seq on human samples (fig 4). Nat Genet (2015) ncbi
Bethyl
rabbit polyclonal
  • chromatin immunoprecipitation; mouse; loading ...; fig 2e
  • western blot; mouse; loading ...; fig 2d
In order to explore the contributions of Brd2 and Brd4 during mouse T helper 17 cell differentiation, Bethyl NIPBL antibody (Bethyl Laboratory, A301-779A) was used in chromatin immunoprecipitation on mouse samples (fig 2e) and in western blot on mouse samples (fig 2d). Mol Cell (2017) ncbi
Articles Reviewed
  1. Cheung K, Zhang F, Jaganathan A, Sharma R, Zhang Q, Konuma T, et al. Distinct Roles of Brd2 and Brd4 in Potentiating the Transcriptional Program for Th17 Cell Differentiation. Mol Cell. 2017;65:1068-1080.e5 pubmed publisher
  2. Bot C, Pfeiffer A, Giordano F, Manjeera D, Dantuma N, Ström L. Independent mechanisms recruit the cohesin loader protein NIPBL to sites of DNA damage. J Cell Sci. 2017;130:1134-1146 pubmed publisher
  3. Izumi K, Nakato R, Zhang Z, Edmondson A, Noon S, Dulik M, et al. Germline gain-of-function mutations in AFF4 cause a developmental syndrome functionally linking the super elongation complex and cohesin. Nat Genet. 2015;47:338-44 pubmed publisher