This is a Validated Antibody Database (VAD) review about rat carnitine deficiency associated gene expressed in ventricle 1, based on 4 published articles (read how Labome selects the articles), using carnitine deficiency associated gene expressed in ventricle 1 antibody in all methods. It is aimed to help Labome visitors find the most suited carnitine deficiency associated gene expressed in ventricle 1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
carnitine deficiency associated gene expressed in ventricle 1 synonym: Cdv-1; Cdv1; intraflagellar transport protein 81 homolog; carnitine deficiency-associated gene expressed in ventricle 1; carnitine deficiency-associated protein expressed in ventricle 1; intraflagellar transport 81 homolog

Proteintech Group
rabbit polyclonal
  • immunocytochemistry; human; 1:50; loading ...; fig 3B
Proteintech Group carnitine deficiency associated gene expressed in ventricle 1 antibody (Proteintech, 11744-1-AP) was used in immunocytochemistry on human samples at 1:50 (fig 3B). Methods Cell Biol (2016) ncbi
rabbit polyclonal
  • western blot; human; 1:1000; loading ...; fig 4b
In order to suggest that IFT52 mutations result in a ciliopathy with primary effects on the skeleton, Proteintech Group carnitine deficiency associated gene expressed in ventricle 1 antibody (ProteinTech, 11744-1-AP) was used in western blot on human samples at 1:1000 (fig 4b). Hum Mol Genet (2016) ncbi
rabbit polyclonal
  • immunocytochemistry; dog; 1:100; loading ...; fig s1c
In order to study primary ciliogenesis in polarized epithelial cells, Proteintech Group carnitine deficiency associated gene expressed in ventricle 1 antibody (Proteintech, 11744-1-AP) was used in immunocytochemistry on dog samples at 1:100 (fig s1c). J Cell Biol (2016) ncbi
rabbit polyclonal
  • western blot; human; 1:1000; fig 4
Proteintech Group carnitine deficiency associated gene expressed in ventricle 1 antibody (Proteintech, 11744-1-AP) was used in western blot on human samples at 1:1000 (fig 4). Nat Cell Biol (2015) ncbi
Articles Reviewed
  1. Kim M, Froese C, Xie H, Trimble W. Immunofluorescent staining of septins in primary cilia. Methods Cell Biol. 2016;136:269-83 pubmed publisher
  2. Zhang W, Taylor S, Nevarez L, Lachman R, Nickerson D, Bamshad M, et al. IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome. Hum Mol Genet. 2016;25:4012-4020 pubmed publisher
  3. Bernabé Rubio M, Andrés G, Casares Arias J, Fernández Barrera J, Rangel L, Reglero Real N, et al. Novel role for the midbody in primary ciliogenesis by polarized epithelial cells. J Cell Biol. 2016;214:259-73 pubmed publisher
  4. Raman M, Sergeev M, Garnaas M, Lydeard J, Huttlin E, Goessling W, et al. Systematic proteomics of the VCP-UBXD adaptor network identifies a role for UBXN10 in regulating ciliogenesis. Nat Cell Biol. 2015;17:1356-69 pubmed publisher