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Mucolipin

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Cation 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.

Below are the list of possible Mucolipin products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Mucolipin-1

 Mucolipin-1 ELISA Kit
 Mucolipin-1 Recombinant
 Mucolipin-1 Antibody
Also known as Mucolipin-1 (MG-2) (Mucolipidin).
mucolipin 1: Cation 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. 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
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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. Belongs to the transient receptor (TC 1.A.4) family. Polycystin subfamily. MCOLN1 sub-subfamily.

Protein type: Channel, cation; Membrane protein, integral; Membrane protein, multi-pass; Transporter, ion channel

Chromosomal Location of Human Ortholog: 19p13.2

Cellular Component: cytoplasm; endosome membrane; lysosomal membrane; plasma membrane; receptor complex

Molecular Function: calcium channel activity; iron ion transmembrane transporter activity

Biological Process: transferrin transport

Disease: Mucolipidosis Iv
 MCOLN1 ELISA Kit
 MCOLN1 Recombinant
 MCOLN1 Antibody
 ML4 ELISA Kit
 ML4 Recombinant
 ML4 Antibody
 MSTP080 ELISA Kit
 MSTP080 Recombinant
 MSTP080 Antibody
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Mucolipin-2

 Mucolipin-2 ELISA Kit
 Mucolipin-2 Recombinant
 Mucolipin-2 Antibody
MCOLN2: Belongs to the transient receptor (TC 1.A.4) family. Polycystin subfamily. MCOLN2 sub-subfamily. 2 isoforms of the human protein are produced by alternative splicing

Protein type: Membrane protein, integral; Membrane protein, multi-pass
 Mcoln2 ELISA Kit
 Mcoln2 Recombinant
 Mcoln2 Antibody
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Mucolipin-3

 Mucolipin-3 ELISA Kit
 Mucolipin-3 Recombinant
 Mucolipin-3 Antibody
MCOLN3: one of members of the mucolipin cation channel proteins. Mutation studies of the highly similar protein in mice have shown that the protein is found in cochlea hair cells, and mutant mice show early-onset hearing loss and balance problems. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]

Protein type: Channel, cat
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ion; Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 1p22.3

Cellular Component: plasma membrane

Molecular Function: calcium channel activity
 MCOLN3 ELISA Kit
 MCOLN3 Recombinant
 MCOLN3 Antibody
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