Background：This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene.
仕様
Synonyms：AIE 75 ,AIE75,Antigen NY CO 38/NY CO 37,Antigen NY-CO-38/NY-CO-37,Autoimmune enteropathy related antigen AIE 75,Autoimmune enteropathy related antigen AIE75,Autoimmune enteropathy-related antigen AIE-75,Deafness autosomal recessive 18,DFNB 18,DFNB18,Harmonin,NY CO 37 ,NY CO 38 ,PDZ 45 ,PDZ 73,PDZ 73 protein ,PDZ 73/NY CO 38,PDZ45,PDZ73,PDZ73 protein,Protein PDZ-73,Renal carcinoma antigen NY REN 3,Renal carcinoma antigen NY-REN-3,USH 1C,USH1C,USH1C,Ush1cpst,Usher syndrome 1C （autosomal recessive severe）,Usher syndrome 1C,Usher syndrome type 1C protein,Usher syndrome type-1C protein
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human USH1C
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
