COG7 Antibodies

AND COG7 ELISA kits, COG7 Proteins

Many biological assays use antibodies to detect COG7, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COG7 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COG7 antibodies...

We validate the specificity of these antibodies to COG7 by testing them on tissues known to express COG7 positively and negatively. Browse below to find the COG7 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.

Previous: Septin9 Next: SNX29

COG7 Infographic by Boster Bio

All COG7 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

COG7 (NM_153603) Human Recombinant Protein

$1062
Cat # PROTP83436
20 µg

COG7 (NM_153603) Human Over-expression Lysate

Human

$628
Cat # LS091949
100 µg

COG7 Overview

Facts about Conserved oligomeric Golgi complex subunit 7.

COG7 3D structure. Source: alphafold

Conserved oligomeric Golgi complex subunit 7 (COG7)

Required for normal Golgi function. .

Gene Information

Human
Gene Name:	COG7
Uniprot:	P83436
Entrez:	91949

Family

Belongs to:

COG7 family

Alternative Names

CDG2E; component of oligomeric golgi complex 7COG complex subunit 7; conserved oligomeric Golgi complex subunit 7

Molecular Weight

Mass (kDA):
86.344 kDA

Genomic Context


Human

Location:	16p12.2
Sequence:	16; NC_000016.10 (23388493..23453215, complement)

Subcellular Localizations

Golgi apparatus membrane; Peripheral membrane protein.

Diseases

Congenital Disorders
Congenital Disorders Of Glycosylation
Failure To Thrive
Inborn Errors Of Metabolism
Growth Retardation
Metabolic Diseases
Microcephaly
Congenital Abnormality
Cutis Laxa
De Novo Mutation
Muscle Hypotonia

Fetal Growth Retardation
Pseudo-obstruction
Ventricular Septal Defects
Impairment (finding)
Menkes Kinky Hair Syndrome
Dermatologic Disorders

Interacting Proteins

COG4
COG5
TAX1BP1
Traf5

Pathways

Glycosylation
Transport
Protein Glycosylation
Localization
Secretory Pathway
Intracellular Transport
Translation
Membrane Fusion

Rna Interference
Fucosylation

PTMs

Glycosylation

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COG7

References

PMID: 11980916 by Ungar D., et al. Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function.

PMID: 15107842 by Wu X., et al. Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder.