MKS1 Polyclonal Antibody

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.

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

Immunogen: Fusion protein of human MKS1

Swissprot: Q9NXB0
Gene Accession: BC010061

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 0.84 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.