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The protein encoded by COG7 resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Additionally we are shipping COG7 Antibodies (57) and COG7 Proteins (6) and many more products for this protein.
Cog7 is an upstream component in a gio-Rab11 pathway controlling membrane addition during cytokinesis.
Targeted silencing of components of lobe B of the COG (show TG ELISA Kits) complex, namely COG5 (show COG5 ELISA Kits), COG6 (show COG6 ELISA Kits), COG7 and COG8 (show COG8 ELISA Kits), inhibited HIV-1 replication
Cog5 (show COG5 ELISA Kits)-Cog7 crystal structure reveals interactions essential for the function of a multisubunit tethering complex.
COG5 (show COG5 ELISA Kits)- and COG7 subunits play distinctive roles in controlling Golgi structure and function
Retrograde transport of multiple Golgi proteins to the ER in COG-7-deficient patient fibroblasts via brefeldin A-induced tubules was significantly slower than occurs in normal fibroblasts.
A homozygous, intronic splice site mutation (c.169+4A>C) of the COG7 gene was identified in 3 patients with Congenital Disorder of Glycosylation type IIe.
A new mutation in COG7 extends the spectrum of COG (show TG ELISA Kits) subunit deficiencies.
The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.
, component of oligomeric golgi complex 7
, conserved oligomeric Golgi complex subunit 7
, conserved oligomeric Golgi complex subunit 7-like
, COG complex subunit 7