WD Repeat Domain 19 (WDR19) (AA 1-437) anticorps

Détails pour le produit réf. ABIN528302
Antigène
  • RGD1306997
  • WDR19
  • pwdmp
  • ATD5
  • CED4
  • DYF-2
  • IFT144
  • NPHP13
  • ORF26
  • Oseg6
  • PWDMP
  • C330027H04Rik
  • D330023L08Rik
  • DYF2
  • Ift144
  • mKIAA1638
  • WD repeat domain 19
  • WD repeat-containing protein 19
  • Wdr19
  • WDR19
  • wdr19
  • LOC100461090
Épitope
AA 1-437
6
4
1
Reactivité
Humain
39
4
4
Hôte
Souris
36
3
Clonalité
Polyclonal
Conjugué
Inconjugué
3
2
2
2
2
2
2
2
2
1
1
1
1
1
Application
Western Blotting (WB)
15
13
10
4
4
3
2
2
Options
Marque MaxPab®
Immunogène WDR19 (AAH32578.1, 1 a.a. ~ 437 a.a) full-length human protein.
Immunogen sequence: MKRIFSLLEK TWLGAPIQFA WQKTSGNYLA VTGADYIVKI FDRHGQKRSE INLPGNCVAM DWDKDGDVLA VIAEKSSCIY LWDANTNKTS QLDNGMRDQM SFLLWSKVGS FLAVGTVKGN LLIYNHQTSR KIPVLGKHTK RITCGCWNAE NLLALGGEDK MITVSNQEGD TIRQTQVRSE PSNMQFFLMK MDDRTSAAES MISVVLGKKT LFFLNLNEPD NPADLEFQQD FGNIVCYNWY GDGRIMIGFS CGHFVVISTH TGELGQEIFQ ARNHKDNLTS IAVSQTLNKV ATCGDNCIKI QDLVDLKDMY VILNLDEENK GLGTLSWTDD GQLLALSTQR GSLHVFLTKL PILGDACSTR IAYLTSLLEV TVANPVEGEL PITVSVDVEP NFVAVGLYHL AVGMNNRAWF YVLGENAVKK IERYGVSGNS SQYLPSF
 Réactivité croisée Humain
Antigène
Autre désignation WDR19 (WDR19 Antibody Extrait)
Sujet Full Gene Name: WD repeat domain 19
Synonyms: FLJ23127,KIAA1638,ORF26,PWDMP
ID gène 57728
Pathways Signalisation Hedgehog
Indications d'application Optimal working dilution should be determined by the investigator.
Commentaires

Product Quality tested by: Antibody reactive against mammalian transfected lysate.

Restrictions For Research Use only
Buffer In 1x PBS, pH 7.4
Conseil sur la manipulation Aliquot to avoid repeated freezing and thawing.
Stock -20 °C
Stockage commentaire Store at -20 °C or lower. Aliquot to avoid repeated freezing and thawing.
Images (Fournisseur)
Western Blotting (WB) image for anti-WD Repeat Domain 19 (WDR19) (AA 1-437) antibody (ABIN528302) Western Blot analysis of WDR19 expression in transfected 293T cell line by WDR19 MaxP...
Produit citée dans: Chaya, Omori, Kuwahara, Furukawa: "ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport." dans: 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." dans: 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. ..." dans: American journal of human genetics, Vol. 89, Issue 5, pp. 634-43, 2011 (PubMed).

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