MKS1 Polyclonal Antibody | G-AB-04417

MKS1 Polyclonal Antibody | G-AB-04417 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas:

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC010061

Clonality: Polyclonal

Immunogen: Fusion protein of human MKS1

Clone #:

Conjugation: Unconjugated

Swissprot: Q9NXB0

Santa Cruz:

Calculated MW: 65 kDa

Observed MW: Refer to figures

Concentration: 0.9 mg/mL

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

Purification method: Antigen affinity purification

Application: WB, IHC, ELISA

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

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

MKS1 Polyclonal Antibody DataSheet