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Bardet-Biedl syndrome 12 protein

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Below are the list of possible Bardet-Biedl syndrome 12 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 12 protein

 Bardet-Biedl syndrome 12 protein ELISA Kit
 Bardet-Biedl syndrome 12 protein Recombinant
 Bardet-Biedl syndrome 12 protein Antibody
BBS12: 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 BBS12 are the cause of Bardet-Biedl syndrome type 12 (BBS12). 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. Secondary features include diabetes mellitus, hypertension and congenital heart disease. A relatively high incidence of BBS is found in the mixed Arab populations of Kuwait and in Bedouin tribes throughout the Middle East, most likely due to the high rate of consaguinity in these populations and a founder effect. BBS12 seems to be rarely involved in oligogenic inheritance. Belongs to the TCP-1 chaperonin family. BBS12 subfamily.

Chromosomal Location of Human Ortholog: 4q27

Cellular Component: chaperonin-containing T-complex

Molecular Function: protein binding; unfolded protein binding

Biological Process: 'de novo' protein folding; chaperone-mediated protein complex assembly; negative regulation of fat cell differentiation

Disease: Bardet-biedl Syndrome 12
 BBS12 ELISA Kit
 BBS12 Recombinant
 BBS12 Antibody
 C4orf24 ELISA Kit
 C4orf24 Recombinant
 C4orf24 Antibody
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Bardet-Biedl syndrome 12 protein homolog

 Bardet-Biedl syndrome 12 protein homolog ELISA Kit
 Bardet-Biedl syndrome 12 protein homolog Recombinant
 Bardet-Biedl syndrome 12 protein homolog Antibody
BBS12: 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 BBS12 are the cause of Bardet-Biedl syndrome type 12 (BBS12). 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. Secondary features include diabetes mellitus, hypertension and congenital heart disease. A relatively high incidence of BBS is found in the mixed Arab populations of Kuwait and in Bedouin tribes throughout the Middle East, most likely due to the high rate of consaguinity in these populations and a founder effect. BBS12 seems to be rarely involved in oligogenic inheritance. Belongs to the TCP-1 chaperonin family. BBS12 subfamily.

Biological Process: chaperone-mediated protein complex assembly; eating behavior; intraflagellar transport; negative regulation of fat cell differentiation; photoreceptor cell maintenance
 Bbs12 ELISA Kit
 Bbs12 Recombinant
 Bbs12 Antibody
 Gm1805 ELISA Kit
 Gm1805 Recombinant
 Gm1805 Antibody
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