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Alstrom syndrome protein

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Involved in PCM1-dependent intracellular transport. Required, directly or indirectly, for the localization of NCAPD2 to the proximal ends of centrioles. Required for proper formation and/or maintenance of primary cilia (PC), microtubule-based structures that protrude from the surface of epithelial cells.

Below are the list of possible Alstrom syndrome protein 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.
 

Alstrom syndrome protein 1

 Alstrom syndrome protein 1 ELISA Kit
 Alstrom syndrome protein 1 Recombinant
 Alstrom syndrome protein 1 Antibody
ALMS1: Involved in PCM1-dependent intracellular transport. Required, directly or indirectly, for the localization of NCAPD2 to the proximal ends of centrioles. Required for proper formation and/or maintenance of primary cilia (PC), microtubule-based structures that protrude from the surface of epithelial cells. Defects in ALMS1 are the cause of Alstrom syndrome (ALMS). Alstrom syndrome is a rare a
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utosomal recessive disorder characterized by progressive cone-rod retinal dystrophy, neurosensory hearing loss, early childhood obesity and type 2 diabetes mellitus. Dilated cardiomyopathy, acanthosis nigricans, male hypogonadism, hypothyroidism, developmental delay and hepatic dysfunction can also be associated with the syndrome. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Cell cycle regulation

Chromosomal Location of Human Ortholog: 2p13

Cellular Component: centriole; centrosome; cytoplasm; cytosol; nucleus

Molecular Function: alpha-actinin binding; protein binding

Biological Process: endosome transport; G2/M transition of mitotic cell cycle; regulation of stress fiber formation

Disease: Alstrom Syndrome
 ALMS1 ELISA Kit
 ALMS1 Recombinant
 ALMS1 Antibody
 KIAA0328 ELISA Kit
 KIAA0328 Recombinant
 KIAA0328 Antibody
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Alstrom syndrome protein 1 homolog

 Alstrom syndrome protein 1 homolog ELISA Kit
 Alstrom syndrome protein 1 homolog Recombinant
 Alstrom syndrome protein 1 homolog Antibody
ALMS1: Involved in PCM1-dependent intracellular transport. Required, directly or indirectly, for the localization of NCAPD2 to the proximal ends of centrioles. Required for proper formation and/or maintenance of primary cilia (PC), microtubule-based structures that protrude from the surface of epithelial cells. Defects in ALMS1 are the cause of Alstrom syndrome (ALMS). Alstrom syndrome is a rare a
>>>
utosomal recessive disorder characterized by progressive cone-rod retinal dystrophy, neurosensory hearing loss, early childhood obesity and type 2 diabetes mellitus. Dilated cardiomyopathy, acanthosis nigricans, male hypogonadism, hypothyroidism, developmental delay and hepatic dysfunction can also be associated with the syndrome. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Cell cycle regulation

Cellular Component: centriole; centrosome; cytoplasm; nucleus

Molecular Function: alpha-actinin binding

Biological Process: calcium-mediated signaling; cell glucose homeostasis; cholesterol homeostasis; endosome transport; epithelial cell proliferation; establishment of planar polarity; fat cell differentiation; glucose homeostasis; inner ear receptor stereocilium organization and biogenesis; lipid metabolic process; negative regulation of apoptosis; negative regulation of multicellular organism growth; ovulation; regulation of fat cell differentiation; regulation of stress fiber formation; retinal rod cell development; sensory perception of sound; spermatid development
 Alms1 ELISA Kit
 Alms1 Recombinant
 Alms1 Antibody
 Kiaa0328 ELISA Kit
 Kiaa0328 Recombinant
 Kiaa0328 Antibody
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