MKS1 Polyclonal Antibody | E-AB-19009

MKS1 Polyclonal Antibody | E-AB-19009 | Gentaur UK, US & Europe Distribution

Type: Polyclonal Antibody

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

Application: WB, IHC, ELISA

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Reserch Areas: N/A

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.

Concentration: 0.9 mg/mL

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

Immunogen: Fusion protein of human MKS1

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

Purification Method: Antigen affinity purification

Dilution: WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000

Clone: N/A

Conjugation: Unconjugated

Molecular Weight(Calculated): 65 kDa

Molecular Weight(Observed): Refer to figures