Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
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 Proteins (6) and many more products for this protein.
Showing 10 out of 60 products:
Human Monoclonal COG7 Primary Antibody for IF, WB - ABIN393730
Zeevaert, Foulquier, Cheillan, Cloix, Guffon, Sturiale, Garozzo, Matthijs, Jaeken: A new mutation in COG7 extends the spectrum of COG subunit deficiencies. in European journal of medical genetics 2009
Show all 5 references for 393730
Human Polyclonal COG7 Primary Antibody for ELISA, WB - ABIN308445
Oka, Vasile, Penman, Novina, Dykxhoorn, Ungar, Hughson, Krieger: Genetic analysis of the subunit organization and function of the conserved oligomeric golgi (COG) complex: studies of COG5- and COG7-deficient mammalian cells. in The Journal of biological chemistry 2005
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 Antibodies) complex, namely COG5 (show COG5 Antibodies), COG6 (show COG6 Antibodies), COG7 and COG8 (show COG8 Antibodies), inhibited HIV-1 replication
Cog5 (show COG5 Antibodies)-Cog7 crystal structure reveals interactions essential for the function of a multisubunit tethering complex.
COG5 (show COG5 Antibodies)- 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 Antibodies) 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