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.

Codice: E-AB-19009_20μL | Marca: Elabscience | Confezionamento: 20μL

Specie: Human;Mouse;RatIsotipo: IgGConiugazione: Unconjugated

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Codice: E-AB-19009_20μL
Marca: Elabscience
Specie target: Human;Mouse;Rat
Host: Rabbit
Concentrazione: 0.9 mg/mL
Link: Apri link
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: WB;IHC
Diluizione: WB 1:500-1:2000;IHC 1:30-1:150
Simbolo target: MKS1
Ig target: 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
Area di ricerca: Tags;Cell Markers

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