Rabbit antibody to Mucolipin 1

FUNCTION: Cationic channel probably playing a role in the endocytic pathway and in the control of membrane trafficking of proteins and lipids. Could play a major role in Ca(2+) transport regulating lysosomal exocytosis.
SUBUNIT: Forms multimeric complexes.
SUBCELLULAR LOCATION: Cell membrane; Multi-pass membrane protein. Late endosome membrane; Multi-pass membrane protein. Lysosome membrane; Multi-pass membrane protein.
TISSUE SPECIFICITY: Widely expressed in adult and fetal tissues.
DISEASE: Defects in MCOLN1 are the cause of mucolipidosis type IV (MLIV), also known as sialolipidosis. MLIV is an autosomal recessive lysosomal storage disorder characterized by severe psychomotor retardation and ophthalmologic abnormalities, including corneal opacity, retinal degeneration and strabismus. Storage bodies of lipids and water-soluble substances are seen by electron microscopy in almost every cell type of the patients. Most patients are unable to speak or walk independently and reach a maximal developmental level of 1-2 years. All patients have constitutive achlorhydia associated with a secondary elevation of serum gastrin levels. MLIV may be due to a defect in sorting and/or transport along the late endocytic pathway. MLIV is found at relatively high frequency among Ashkenazi Jews.

IHC, WB. A dilution of 1: 1000 to 1:3000 is recommended. The optimal dilution should be determined by the end user. Not yet tested in other applications.

12 months after reconstitution

1. Bassi M.T, et al. Am. J. Hum. Genet. 67:1110-1120(2000).

A synthetic peptide from mouse Mucolipin 1 conjugated to blue carrier protein was used as the antigen. The peptide is homologous in human, monkey and rat.

http://www.uniprot.org/uniprot/Q99J21
http://www.uniprot.org/uniprot/Q9GZU1
http://www.uniprot.org/uniprot/Q60HE8
http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=XP_213684.3

Polyclonal

Lyophilised