Olfactory receptor 51V1 Antibodies

AND OR51V1 ELISA kits, Olfactory receptor 51V1 Proteins

Many biological assays use antibodies to detect Olfactory receptor 51V1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Olfactory receptor 51V1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Olfactory receptor 51V1 antibodies...

We validate the specificity of these antibodies to Olfactory receptor 51V1 by testing them on tissues known to express OR51V1 positively and negatively. Browse below to find the OR51V1 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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OR51V1 Infographic by Boster Bio

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Anti-O51V1 OR51V1 Antibody

Western blot analysis of lysates from Jurkat cells, primary antibody was diluted at 1:1000, 4°over night

Human

ELISA, WB

$380
Cat # A16290
100ul

OR51V1 Overview

Facts about Olfactory receptor 51V1.

OR51V1 3D structure. Source: alphafold

Olfactory receptor 51V1 (OR51V1)

Odorant receptor. .

Gene Information

Human
Gene Name:	OR51V1
Uniprot:	Q9H2C8
Entrez:	283111

Family

Belongs to:

G-protein coupled receptor 1 family

Alternative Names

Olfactory receptor 51V1

Molecular Weight

Mass (kDA):
36.749 kDA

Genomic Context


Human

Location:	11p15.4
Sequence:	11; NC_000011.10 (5199735..5200700, complement)

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

PTMs

Disulfide bond

Glycoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/OR51V1

References

PMID: 11121057 by Bulger M., et al. Comparative structural and functional analysis of the olfactory receptor genes flanking the human and mouse beta-globin gene clusters.

PMID: 26282398 by Dahmani M., et al. EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss.