|Western Blot (WB)||1:300-1:2000|
|Tested Species reactivity||Mouse|
|Host / Isotype||Rabbit / IgG|
|Immunogen||A synthetic peptide from mouse Dfna5h deafness|
|Storage buffer||whole serum|
|Storage conditions||Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.|
Reconstitute with 100 ul of distilled water.
Expressed in cochlea. Low level of expression in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas, with highest expression in placenta. Defects in DFNA5 are the cause of non-syndromic sensorineural deafness autosomal dominant type
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: deafness, autosomal dominant 5 homolog; Non-syndromic hearing impairment protein 5 homolog; nonsyndromic hearing impairment protein
Gene Aliases: 2310037D07Rik; 4932441K13Rik; Dfna5; Dfna5h; EG14210; Fin15
UniProt ID: (Mouse) Q9Z2D3
Entrez Gene ID: (Mouse) 54722
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