Description
| Antibody Name: | WDR19 Antibody (PACO50834) | 
| Antibody SKU: | PACO50834 | 
| Size: | 50ug | 
| Host Species: | Rabbit | 
| Tested Applications: | ELISA, IHC, IF | 
| Recommended Dilutions: | ELISA:1:2000-1:10000, IHC:1:20-1:200, IF:1:50-1:200 | 
| Species Reactivity: | Human | 
| Immunogen: | Recombinant Human WD repeat-containing protein 19 protein (45-226AA) | 
| Form: | Liquid | 
| Storage Buffer: | Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 | 
| Purification Method: | >95%, Protein G purified | 
| Clonality: | Polyclonal | 
| Isotype: | IgG | 
| Conjugate: | Non-conjugated | 
|  | Immunohistochemistry of paraffin-embedded human placenta tissue using PACO50834 at dilution of 1:100. | 
|  | Immunofluorescent analysis of A549 cells using PACO50834 at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L). | 
|  | Immunohistochemistry of paraffin-embedded human liver cancer using PACO50834 at dilution of 1:100. | 
| Background: | Component of the IFT complex A (IFT-A), a complex required for retrograde ciliary transport. Involved in cilia function and/or assembly (By similarity). Associates with the BBSome complex to mediate ciliary transport (By similarity). | 
| Synonyms: | WD repeat-containing protein 19 (Intraflagellar transport 144 homolog), WDR19, IFT144 KIAA1638 | 
| UniProt Protein Function: | |
| UniProt Protein Details: | |
| NCBI Summary: | The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] | 
| UniProt Code: | Q8NEZ3 | 
| NCBI GenInfo Identifier: | 21619140 | 
| NCBI Gene ID: | 57728 | 
| NCBI Accession: | BC032578 | 
| UniProt Secondary Accession: | Q8NEZ3,Q8N5B4, Q9H5S0, Q9HCD4, B5MEF2 | 
| UniProt Related Accession: | Q8NEZ3 | 
| Molecular Weight: | 53,573 Da | 
| NCBI Full Name: | Homo sapiens WD repeat domain 19, mRNA | 
| NCBI Synonym Full Names: | WD repeat domain 19 | 
| NCBI Official Symbol: | WDR19 | 
| NCBI Official Synonym Symbols: | ATD5; CED4; DYF-2; ORF26; Oseg6; PWDMP; SRTD5; IFT144; NPHP13 | 
| NCBI Protein Information: | WD repeat-containing protein 19 | 
| UniProt Protein Name: | |
| UniProt Synonym Protein Names: | |
| Protein Family: | WD repeat-containing protein | 
| UniProt Gene Name: | |
| UniProt Entry Name: | 
 
 
             
             
             
             
            