| Background: | SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition. | 
| Applications: | ELISA, IHC | 
| Name of antibody: | SNX29 | 
| Immunogen: | Synthetic peptide of human SNX29 | 
| Full name: | sorting nexin 29 | 
| Synonyms: | RUNDC2A; A-388D4.1 | 
| SwissProt: | Q8TEQ0 | 
| ELISA Recommended dilution: | 1000-2000 | 
| IHC positive control: | Human liver cancer and Human colon cancer | 
| IHC Recommend dilution: | 25-100 | 
	
	 
 
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