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For research use only.

Verified Samples Verified Samples in IHC: Human tonsil
Dilution IHC 1:50-1:300
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications IHC
Clonality Polyclonal
Immunogen Fusion protein of human MKS1
Abbre MKS1
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
Swissprot
Cellular Localization Cytoplasm>cytoskeleton>cilium basal body. Cytoplasm>cytoskeleton>microtubule organizing center>centrosome. Localizes at the transition zone, a region between the basal body and the ciliary axoneme.
Concentration 0.84 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Antigen affinity purification
Research Areas Tags,  Cell Markers
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
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.
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Unconjugated

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