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Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59)
less commonly
Paraspeckles often co-localize with splicing speckles
NAD(+) ADP ribosyltransferase 2
Catalogue Numbers: BS8964-50
COA3 Polyclonal Antibody - E-AB-90892 Magnetofectamine Defects in this gene areCOA3 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 90892 60, E AB 90892 120, E AB 90892 200 Citations, Manuals and MSDS Available upon request. Abbreviation: COA3 Target Synonym: COA3; CCDC56; COX25; HSPC009; MITRAC12 Conjugation: Unconjugated Host: Rabbit Species Reactivity: Human Application: WB Isotype: IgG Clonality: Polyclonal UNIProt ID: Q9Y2R0 Background: This gene encodes a member of the cytochrome c oxidase assembly
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