COG2 Antibodies

AND COG2 ELISA kits, COG2 Proteins

Many biological assays use antibodies to detect COG2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with COG2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop COG2 antibodies...

We validate the specificity of these antibodies to COG2 by testing them on tissues known to express COG2 positively and negatively. Browse below to find the COG2 antibody that suites your experiment. We have 3 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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COG2 Infographic by Boster Bio

All COG2 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-COG2 Antibody

Human, Mouse, Rat

IHC, WB

$405
Cat # A09800
100ul

COG2 (NM_007357) Human Recombinant Protein

$813
Cat # PROTQ14746
20 µg

COG2 (NM_007357) Human Over-expression Lysate

Human

$628
Cat # LS022796
100 µg

COG2 Overview

Facts about Conserved oligomeric Golgi complex subunit 2.

COG2 3D structure. Source: alphafold

Conserved oligomeric Golgi complex subunit 2 (COG2)

Required for normal Golgi morphology and function. .

Gene Information

Human
Gene Name:	COG2
Uniprot:	Q14746
Entrez:	22796

Family

Belongs to:

COG2 family

Alternative Names

component of oligomeric golgi complex 2COG complex subunit 2; conserved oligomeric Golgi complex protein 2; conserved oligomeric Golgi complex subunit 2; LDLCbrefeldin A-sensitive, peripheral Golgi protein; low density lipoprotein receptor defect C complementing; Low density lipoprotein receptor defect C-complementing protein

Molecular Weight

Mass (kDA):
83.208 kDA

Genomic Context


Human

Location:	1q42.2
Sequence:	1; NC_000001.11 (230642481..230693982)

Subcellular Localizations

Golgi apparatus membrane; Peripheral membrane protein; Cytoplasmic side.

Diseases

Congenital Disorders
Congenital Disorders Of Glycosylation
Hyperlipidemia
Alzheimer's Disease
Hypokinesia

Interacting Proteins

COG4
MTUS2

Pathways

Transport
Glycosylation
Secretory Pathway
Localization
Vesicle Docking
Secretion
Vesicle Targeting
Vesicle Transport
Intracellular Transport
Golgi Localization
Protein Secretion
Protein Transport

Vesicle Fusion
Golgi Vesicle Docking
Translation
Cell Growth
Interphase
Rna Interference

PTMs

Glycosylation

Cleavage

Research Areas

Golgi Apparatus Markers

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/COG2

References

PMID: 7962052 by Podos S.D., et al. LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function.

PMID: 24784932 by Kodera H., et al. Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation.