Background：The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 （MCOPS9）. Several transcript variants encoding a few different isoforms have been found for this gene.
仕様
Synonyms：MCOPCB8,MCOPS9,PP14296,Stimulated by retinoic acid 6 homolog,Stimulated by retinoic acid gene 6 protein homolog,STRA6,STRA6
Host：Rabbit
Reactivity：Human
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human STRA6
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）：64220
Swissprot：Q9BX79
Isotype：IgG
Research Areas：Metabolism, Developmental biology, Signal transduction, Stem cells
