COG8 Antilichaam

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.

84342

Q96MW5

Human

Recombinant fusion protein containing a sequence corresponding to amino acids 394-612 of human COG8 (NP_115758.3) .

Unconjugated

Primary Antibodies

Signal Transduction

Affinity purification

Jurkat

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 68kDa

IgG

WB: 1:500 - 1:2000

COG8

A-431

Component of oligomeric golgi complex 8

Homo sapiens

Dependent on RIC1, conserved oligomeric golgi complex component 8, FLJ22315, DOR1, component of oligomeric golgi complex 8, COG8, CDG2H

WB

Liquid