Background：The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 （DFNB49）. Two transcript variants encoding different isoforms have been found for this gene.
仕様
Synonyms：deafness, autosomal recessive 49,DFNB49,MALD2,MARVD2,MARVEL （membrane-associating） domain containing 2,MARVEL domain containing protein 2,MARVEL domain-containing protein 2,Marveld2,TRIC,Tricellulin
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC
Concentration：1mg/ml
Immunogen：A synthetic peptide of human MARVELD2
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
