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WDR19 抗体

(WD Repeat Domain 19 (WDR19))
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains six WD repeats, a clathrin heavy-chain repeat, and three transmembrane domains. This gene is conserved from C. elegans to human. It may participate in androgen-regulated signaling mechanisms or in the vesicular trafficking of androgen-regulated secretory processes. Alternatively spliced transcript variants encoding distinct isoforms have been reported but the full-length nature of one of these variants has not been defined. [provided by RefSeq, Jul 2008].

Active filters:

  • 抗原: WDR19
  • Primary
Catalog no. 产品 适用 宿主 / 克隆类型 应用 价格和交货时间
ABIN7846384
WDR19 抗体 (Center) WDR19 · Primary Antibody 人, 小鼠 兔 Polyclonal
  • WB (Western Blotting: 所列应用)
  • 200 μL
发货至: 中国
Primary Antibody
  • WB (Western Blotting: 所列应用)
适用
人, 小鼠
宿主
兔
克隆形成能力
Polyclonal
标记
unconjugated
抗原表位
Center
产品编号 ABIN7846384

Latest Publications for our WDR19 抗体

Chaya, Omori, Kuwahara, Furukawa: "ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport." in: The EMBO journal, Vol. 33, Issue 11, pp. 1227-42, (2014) (PubMed).

Ashe, Butterfield, Town, Courtney, Cooper, Ferguson, Barry, Olsson, Liem, Parton, Wainwright, Anderson, Whitelaw, Wicking: "Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies." in: Human molecular genetics, Vol. 21, Issue 8, pp. 1808-23, (2012) (PubMed).

Bredrup, Saunier, Oud, Fiskerstrand, Hoischen, Brackman, Leh, Midtbø, Filhol, Bole-Feysot, Nitschké, Gilissen, Haugen, Sanders, Stolte-Dijkstra, Mans, Steenbergen, Hamel, Matignon, Pfundt, Jeanpierre et al.: "Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19. ..." in: American journal of human genetics, Vol. 89, Issue 5, pp. 634-43, (2011) (PubMed).

Jiang, Chiou, Wang, Chien, Ho, Tsai, Lin, Tsai, Li: "Essential role of nephrocystin in photoreceptor intraflagellar transport in mouse." in: Human molecular genetics, Vol. 18, Issue 9, pp. 1566-77, (2009) (PubMed).

Aliases for WDR19 抗体

WD repeat domain 19 (Wdr19) 抗体
WD repeat domain 19 (WDR19) 抗体
WD repeat domain 19 (wdr19) 抗体
WD repeat-containing protein 19 (LOC100461090) 抗体
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C330027H04Rik 抗体
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D330023L08Rik 抗体
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DYF2 抗体
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Ift144 抗体
mKIAA1638 抗体
NPHP13 抗体
ORF26 抗体
Oseg6 抗体
pwdmp 抗体
PWDMP 抗体
RGD1306997 抗体
WDR19 抗体
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