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2 results for "Dfna5 Lysates" in 产品
Dfna5 Lysates
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq]
| Reactivity: | Human |
| Applications: | WB |
![Western Blot: Dfna5 Overexpression Lysate [NBL1-09843]](https://resources.rndsystems.com/images/products/Dfna5-deafness-Overexpression-Lysate-Adult-Normal-Western-Blot-NBL1-09843-img0002.jpg "Western Blot: Dfna5 Overexpression Lysate [NBL1-09843]")
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| Reactivity: | Human |
| Applications: | WB |
![Western Blot: Dfna5 Overexpression Lysate [NBP2-11376]](https://resources.rndsystems.com/images/products/Dfna5-deafness-Overexpression-Lysate-Adult-Normal-Western-Blot-NBP2-11376-img0001.jpg "Western Blot: Dfna5 Overexpression Lysate [NBP2-11376]")
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