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COG6 encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi apparatus. Zusätzlich bieten wir Ihnen COG6 Antikörper (30) und und viele weitere Produktgruppen zu diesem Protein an.
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COG6 is a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus.
study presents 7 additional patients with 4 novel COG6 mutations; genotype-phenotype correlation can be discerned ranging from deep intronic mutations found in Shaheen syndrome as the mildest form to loss-of-function mutations leading to early lethal congenital disorders of glycosylation phenotypes
The aim of this study was to investigate whether the HCP5, TNIP1 (zeige TNIP1 Proteine), TNFAIP3 (zeige TNFAIP3 Proteine), SPATA2 (zeige SPATA2 Proteine) and COG6 genes were genetic risk factors for psoriasis in Chinese population.
Our findings implicate COG6 rs9548934C-->T genotypes and circulating miRNA-1 phenotype in modulating the occurrence and major adverse cardiovascular events of coronary artery disease.
Targeted silencing of components of lobe B of the COG (zeige TG Proteine) complex, namely COG5 (zeige COG5 Proteine), COG6, COG7 (zeige COG7 Proteine) and COG8 (zeige COG8 Proteine), inhibited HIV-1 replication
data implicate COG6 in the pathogenesis of a novel hypohidrotic disorder in humans that is distinct from congenital disorders of glycosylation.
COG6 interaction with SNARE (zeige NAPA Proteine) proteins via universal SNARE (zeige NAPA Proteine)-binding motif of COG6 is important for Golgi complex intergrity.
COG6 rs9548934C-->T polymorphism is associated with lower risk of premature coronary artery disease, especially in female subjects and subjects with lower serum lipid levels.
COG (zeige TG Proteine) directly and positively regulates endosome-to-TGN (zeige TG Proteine) retrograde transport by specific and direct interaction with the t-SNARE (zeige NAPA Proteine) Stx6 (zeige STX6 Proteine) via its Cog6 subunit.
This paper reports a new congenital disorder caused by mutations in the human COG8 (zeige COG8 Proteine) gene and describes the affect this mutation has on the other COG (zeige TG Proteine) components.
This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi apparatus. The encoded protein is organized with conserved oligomeric Golgi complex components 5, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants.
component of oligomeric golgi complex 6
, Conserved oligomeric Golgi complex component 6
, COG complex subunit 6
, complexed with Dor1p 2
, conserved oligomeric Golgi complex protein 6
, conserved oligomeric Golgi complex subunit 6
, potential intra-Golgi transport complex subunit 6