COG1 Antibodies

AND COG1 ELISA kits, COG1 Proteins

Many biological assays use antibodies to detect COG1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COG1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COG1 antibodies...

We validate the specificity of these antibodies to COG1 by testing them on tissues known to express COG1 positively and negatively. Browse below to find the COG1 antibody that suites your experiment. We have 1 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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COG1 Infographic by Boster Bio

All COG1 Products

Product

Figures

Specificity

Applications

Price

Anti-COG1 Antibody (C-term)

Human

$298
Cat # M07344
80 µl

COG1 Overview

Facts about Conserved oligomeric Golgi complex subunit 1.

COG1 3D structure. Source: alphafold

Conserved oligomeric Golgi complex subunit 1 (COG1)

Required for normal Golgi function. .

Gene Information

Human
Gene Name:	COG1
Uniprot:	Q8WTW3
Entrez:	9382

Family

Belongs to:

COG1 family

Alternative Names

COG complex subunit 1; component of oligomeric golgi complex 1CDG2G; conserved oligomeric Golgi complex subunit 1; KIAA1381DKFZp762L1710; LDLBconserved oligomeric Golgi complex protein 1; low density lipoprotein receptor defect B complementing

Molecular Weight

Mass (kDA):
108.978 kDA

Genomic Context


Human

Location:	17q25.1
Sequence:	17; NC_000017.11 (73193055..73208507)

Subcellular Localizations

Golgi apparatus membrane; Peripheral membrane protein; Cytoplasmic side.

Diseases

Congenital Disorders
Congenital Disorders Of Glycosylation
Congenital Abnormality
Stomatitis
Vesicular Stomatitis
Cerebro-costo-mandibular Syndrome
Inborn Errors Of Metabolism
Dysostoses
Physiological Stress
Hypokinesia

Jarcho-levin Syndrome
Dysplasia
Impairment (finding)
Alzheimer's Disease

Interacting Proteins

COG4

Pathways

Glycosylation
Localization
Transport
Protein Glycosylation
Translation
Secretory Pathway
Intracellular Transport
Golgi Localization
Spermatogenesis

Seed Germination
Germination
Rna Interference
Secretion

PTMs

Glycosylation

Cleavage

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COG1

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: 16537452 by Foulquier F., et al. Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.