COG5 Antibodies

AND COG5 ELISA kits, COG5 Proteins

Many biological assays use antibodies to detect COG5, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COG5 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COG5 antibodies...

We validate the specificity of these antibodies to COG5 by testing them on tissues known to express COG5 positively and negatively. Browse below to find the COG5 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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COG5 Infographic by Boster Bio

All COG5 Products

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COG5 (NM_006348) Human Recombinant Protein

Coomassie blue staining of purified COG5 protein

$1249
Cat # PROTQ9UP83
20 µg

COG5 (NM_006348) Human Over-expression Lysate

Human

$960
Cat # LS010466
20 µg, 100 µg

COG5 Overview

Facts about Conserved oligomeric Golgi complex subunit 5.

COG5 3D structure. Source: alphafold

Conserved oligomeric Golgi complex subunit 5 (COG5)

Required for normal Golgi function. .

Gene Information

Human
Gene Name:	COG5
Uniprot:	Q9UP83
Entrez:	10466

Family

Belongs to:

COG5 family

Alternative Names

component of oligomeric golgi complex 5; FLJ44289

Molecular Weight

Mass (kDA):
92.743 kDA

Genomic Context


Human

Location:	7q22.3
Sequence:	7; NC_000007.14 (107201744..107564361, complement)

Subcellular Localizations

Cytoplasm, cytosol. Golgi apparatus membrane; Peripheral membrane protein.

Diseases

Degenerative Polyarthritis
Congenital Disorders
Dysequilibrium Syndrome
Osteoarthritis, Knee
Congenital Disorders Of Glycosylation
Inborn Errors Of Metabolism
Stomatitis
Inflammatory Response
Pseudo-obstruction
Fracture
Ventricular Septal Defects
Hyalinization

Neoplasms
Familial Mediterranean Fever
Uterine Fibroids
Osteoarthritis Of Hip
Impacted Tooth
Microcephaly

Interacting Proteins

COG4
COG7

Pathways

Transport
Glycosylation
Protein Glycosylation
Secretory Pathway
Intracellular Transport
Translation
Localization
Rna Interference

Secretion
Inflammatory Response

PTMs

Glycosylation

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COG5

References

PMID: 9792665 by Walter D.M., et al. Purification and characterization of a novel 13 S hetero-oligomeric protein complex that stimulates in vitro Golgi transport.

PMID: 19690088 by Paesold-Burda P., et al. Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.