Background：This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases （SDR） family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 （biogenesis of lysosomal organelles complex-1, subunit 1） gene.
仕様
Synonyms：11 cis RDH,11 cis retinol dehydrogenase,9 cis retinol specific dehydrogenase,FLJ39337,FLJ97089,HSD17B9,RDH 5,RDH1,Retinol dehydrogenase 1,Retinol dehydrogenase 5 （11 cis/9 cis）,Retinol dehydrogenase 5,SDR9C5,Short chain dehydrogenase/reductase family 9C member 5
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human RDH5
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
