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Bardet-Biedl syndrome 10 protein

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Below are the list of possible Bardet-Biedl syndrome 10 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.
 

Bardet-Biedl syndrome 10 protein

 Bardet-Biedl syndrome 10 protein ELISA Kit
 Bardet-Biedl syndrome 10 protein Recombinant
 Bardet-Biedl syndrome 10 protein Antibody
BBS10: Probable molecular chaperone. Assists the folding of proteins upon ATP hydrolysis. As part of the BBS/CCT complex may play a role in the assembly of BBSome, a complex involved in ciliogenesis regulating transports vesicles to the cilia. Involved in adipogenic differentiation. Defects in BBS10 are the cause of Bardet-Biedl syndrome type 10 (BBS10). Bardet-Biedl syndrome (BBS) is a geneticall
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y heterogeneous, autosomal recessive disorder characterized by usually severe pigmentary retinopathy, early onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. Belongs to the TCP-1 chaperonin family.

Chromosomal Location of Human Ortholog: 12q21.2

Molecular Function: protein binding

Biological Process: chaperone-mediated protein complex assembly; photoreceptor cell maintenance; regulation of protein complex assembly; retinal homeostasis

Disease: Bardet-biedl Syndrome 10
 BBS10 ELISA Kit
 BBS10 Recombinant
 BBS10 Antibody
 C12orf58 ELISA Kit
 C12orf58 Recombinant
 C12orf58 Antibody
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Bardet-Biedl syndrome 10 protein homolog

 Bardet-Biedl syndrome 10 protein homolog ELISA Kit
 Bardet-Biedl syndrome 10 protein homolog Recombinant
 Bardet-Biedl syndrome 10 protein homolog Antibody
BBS10: Probable molecular chaperone. Assists the folding of proteins upon ATP hydrolysis. As part of the BBS/CCT complex may play a role in the assembly of BBSome, a complex involved in ciliogenesis regulating transports vesicles to the cilia. Involved in adipogenic differentiation. Defects in BBS10 are the cause of Bardet-Biedl syndrome type 10 (BBS10). Bardet-Biedl syndrome (BBS) is a geneticall
>>>
y heterogeneous, autosomal recessive disorder characterized by usually severe pigmentary retinopathy, early onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. Belongs to the TCP-1 chaperonin family.

Biological Process: chaperone-mediated protein complex assembly; photoreceptor cell maintenance; regulation of protein complex assembly; retinal homeostasis
 Bbs10 ELISA Kit
 Bbs10 Recombinant
 Bbs10 Antibody
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