Background：This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.
仕様
Synonyms：Brain specific homeobox/POU domain protein 3C,Brain-3C,Brain-specific homeobox/POU domain protein 3C,BRN 3C,Brn-3C,BRN3C,class 4,DFNA 15,DFNA15,MGC138412,PO4F3,POU class 4 homeobox 3,POU domain,POU domain class 4 transcription factor 3,POU4F3,transcription factor 3
Host：Rabbit
Reactivity：Human,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human POU4F3
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB1：500 - 1：2000
Gene_ID（human）：5459
Swissprot：Q15319
Isotype：IgG
Research Areas：Cancer, Epigenetics and Nuclear Signaling, Neuroscience
