ALMS1 Polyclonal Antibody

Ab type

Primary antibody

Background

ALMS1 encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein (ALMS1, centrosome and basal body associated protein) functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations ALMS1 cause Alstrom syndrome. There is a pseudogene for ALMS1 located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined.

Reactivity

Human

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from ALMS1 . at AA range: 1530-1610

Storage Stability

-20°C for one year

Concentration

1 mg/ml

MolecularWeight_Da

460937

synonyms

ALMS1; KIAA0328; Alstrom syndrome protein 1