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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.

Product Datasheet

https://www.prosci-inc.com/?datasheet_sku=15-501

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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