COG8 Antibody
Product Specifications
Background
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.
NCBI Gene ID
84342
Swiss Prot
Q96MW5
Host
Rabbit
Reactivity
Human
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 394-612 of human COG8 (NP_115758.3) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Signal Transduction
Purification
Affinity purification
Positive Control
Jurkat
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 68kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
COG8
Positive Control 2
A-431
NCBI Official Name
Component of oligomeric golgi complex 8
NCBI Organism
Homo sapiens
Other Product Names
Dependent on RIC1, conserved oligomeric golgi complex component 8, FLJ22315, DOR1, component of oligomeric golgi complex 8, COG8, CDG2H
Tested Applications
WB
Physical Properties
Liquid
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