Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance.
BB235941; C87832; CDG2H; COG complex subunit 8; Cog8; Component of oligomeric Golgi complex 8; conserved oligomeric golgi complex component 8; conserved oligomeric Golgi complex protein 8; conserved oligomeric Golgi complex subunit 8; dependent on RIC1; DOR1; MNCb-5704
100 µL
150 µL
100 µL
100 µL
50 µg
100 µg
Searching for an antibody we don't offer? We make custom antibodies for specific targets, species and applications.
More than 18,000 custom antibodies created so far.
Talk to a specialist nowIf an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support