GPR179 Antibodies

AND GPR179 ELISA kits, GPR179 Proteins

Many biological assays use antibodies to detect GPR179, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with GPR179 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop GPR179 antibodies...

We validate the specificity of these antibodies to GPR179 by testing them on tissues known to express GPR179 positively and negatively. Browse below to find the GPR179 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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GPR179 Infographic by Boster Bio

All GPR179 Products

Product

Figures

Specificity

Applications

Price

Anti-GPR179 Antibody

Human, Mouse

$405
Cat # A10399
100ul

Anti-GP179 GPR179 Antibody

Human

IHC

$380
Cat # A10399-1
100ul

GPR179 Overview

Facts about Probable G-protein coupled receptor 179.

GPR179 3D structure. Source: alphafold

Probable G-protein coupled receptor 179 (GPR179)

Orphan receptor, involved in vision. Required for signal transduction through retinal depolarizing bipolar cells.

Gene Information

Human
Gene Name:	GPR179
Uniprot:	Q6PRD1
Entrez:	440435

Family

Belongs to:

G-protein coupled receptor 3 family

Alternative Names

G protein-coupled receptor 179; GPR158L1; GPR158-like 1; probable G-protein coupled receptor 179

Molecular Weight

Mass (kDA):
257.363 kDA

Genomic Context


Human

Location:	17q12
Sequence:	17; NC_000017.11 (38324571..38343956, complement)

Tissue Specificity

Expressed in the retina.

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

Diseases

Night Blindness
Blind Vision
Eye Diseases, Hereditary
Genetic Diseases, X-linked
Retinal Diseases
Myopia
Congenital Stationary Night Blindness

Visual Impairment

Pathways

Signal Transmission
Localization

PTMs

Glycoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/GPR179

References

PMID: 22325361 by Audo I., et al. Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.

PMID: 22325362 by Peachey N.S., et al. GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.