SCNAA Polyclonal Antibody, 20ul Protein Research A mutation in this gene

A mutation in this gene has been associated with selective 25-hydroxyvitamin D deficiency

This protein functions as a negative regulator of the canonical Wnt/beta-catenin signaling cascade

Easy to switch between manual aspiration and continuous aspiration mode

tissue specificity:Expressed abundantly in the lung and neutrophils

when thymine dimers are present

SCNAA Polyclonal Antibody, 20ul Protein Research A mutation in this geneThe protein encoded by this gene is a tetrodotoxin resistant voltage gated sodium channel alpha subunit. The properties of the channel formed by the encoded transmembrane protein can be altered by interaction with different beta subunits. This protein may be involved in the onset of pain associated with peripheral neuropathy. Alternative splicing results in multiple transcript variants.