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The protein encoded by COG4 is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Additionally we are shipping COG4 Proteins (3) and many more products for this protein.
Showing 10 out of 25 products:
Human Polyclonal COG4 Primary Antibody for EIA, WB - ABIN359592
Whyte, Munro: The Sec34/35 Golgi transport complex is related to the exocyst, defining a family of complexes involved in multiple steps of membrane traffic. in Developmental cell 2001
Show all 3 references for ABIN359592
Chicken Polyclonal COG4 Primary Antibody for WB - ABIN2786105
Suzuki, Fujisawa, Ando, Niino, Ohsawa, Shimokata, Ohta: Alcohol dehydrogenase 2 variant is associated with cerebral infarction and lacunae. in Neurology 2004
Show all 2 references for ABIN2786105
Chicken Polyclonal COG4 Primary Antibody for WB - ABIN2786106
Suzuki, Yamashita, Shirota, Sakakibara, Chiba, Mizushima-Sugano, Nakai, Sugano: Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions. in Genome research 2004
Show all 2 references for ABIN2786106
A novel R729W missense mutation in COG4 was associated with the congenital disorder of glycosylation type II.
Study shows that the SM protein, Sly1 (show SCFD1 Antibodies), interacts directly with the conserved oligomeric Golgi (COG (show TG Antibodies)) tethering complex; Sly1 (show SCFD1 Antibodies)-COG (show TG Antibodies) interaction is mediated by the Cog4 subunit, which also interacts with Syntaxin 5 (show STX5 Antibodies) through a different binding site.
The 1.9 A crystal structure of a Cog4 C-terminal fragment, was determined. Arg 729 is found to occupy a key position at the center of a salt bridge network, thereby stabilizing Cog4's small C-terminal domain.
The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.
component of oligomeric golgi complex 4
, Conserved oligomeric Golgi complex subunit 4
, COG complex subunit 4
, complexed with Dor1p
, conserved oligomeric Golgi complex protein 4
, conserved oligomeric Golgi complex subunit 4