Background：The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene.
仕様
Synonyms：B8d3,BBS13,Dysencephalia splanchnocystica,FABB proteome like protein,FLJ20345,Gruber syndrome,Meckel gruber syndrome,Meckel gruber syndrome type 1,Meckel syndrome,Meckel syndrome type 1,Meckel syndrome type 1 protein,Meckel syndrome type 1 protein homolog,MES,MKS 1,MKS,Mks1,MKS1,POC12,POC12 centriolar protein homolog
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human MKS1
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
