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LearnH00057728-B01P
antibody from Novus Biologicals
Targeting: WDR19
DYF-2, FAP66, FLJ23127, IFT144, KIAA1638, NPHP13, ORF26, Oseg6, Pwdmp
Western blot
ImmunocytochemistryAntibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations
- Western blot [1]
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- Product number
- H00057728-B01P - Provider product page
- Provider
- Novus Biologicals
- Proper citation
- Novus Cat#H00057728-B01P, RRID:AB_2215258
- Product name
- Mouse Polyclonal WDR19 Antibody
- Antibody type
- Polyclonal
- Description
- Protein A purified. WDR19 - WD repeat domain 19,
- Reactivity
- Human, Mouse
- Host
- Mouse
- Isotype
- IgG
- Vial size
- 0.05 mg
- Storage
- Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Submitted references Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa.
ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport.
Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies.
Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.
Nguyen TT, Hull S, Roepman R, van den Born LI, Oud MM, de Vrieze E, Hetterschijt L, Letteboer SJF, van Beersum SEC, Blokland EA, Yntema HG, Cremers FPM, van der Zwaag PA, Arno G, van Wijk E, Webster AR, Haer-Wigman L
Journal of medical genetics 2017 Sep;54(9):624-632
Journal of medical genetics 2017 Sep;54(9):624-632
ICK is essential for cell type-specific ciliogenesis and the regulation of ciliary transport.
Chaya T, Omori Y, Kuwahara R, Furukawa T
The EMBO journal 2014 Jun 2;33(11):1227-42
The EMBO journal 2014 Jun 2;33(11):1227-42
Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies.
Ashe A, Butterfield NC, Town L, Courtney AD, Cooper AN, Ferguson C, Barry R, Olsson F, Liem KF Jr, Parton RG, Wainwright BJ, Anderson KV, Whitelaw E, Wicking C
Human molecular genetics 2012 Apr 15;21(8):1808-23
Human molecular genetics 2012 Apr 15;21(8):1808-23
Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.
Bredrup C, Saunier S, Oud MM, Fiskerstrand T, Hoischen A, Brackman D, Leh SM, Midtbø M, Filhol E, Bole-Feysot C, Nitschké P, Gilissen C, Haugen OH, Sanders JS, Stolte-Dijkstra I, Mans DA, Steenbergen EJ, Hamel BC, Matignon M, Pfundt R, Jeanpierre C, Boman H, Rødahl E, Veltman JA, Knappskog PM, Knoers NV, Roepman R, Arts HH
American journal of human genetics 2011 Nov 11;89(5):634-43
American journal of human genetics 2011 Nov 11;89(5):634-43
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Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Western Blot: WDR19 Antibody [H00057728-B01P] - Analysis of WDR19 expression in transfected 293T cell line by WDR19 polyclonal antibody. Lane 1: WDR19 transfected lysate(48.07 KDa). Lane 2: Non-transfected lysate.
