Opalin Antibodies

AND OPALIN ELISA kits, Opalin Proteins

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

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

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OPALIN (NM_033207) Human Over-expression Lysate

Human

$628
Cat # LS093377
20 µg, 100 µg

OPALIN Overview

Facts about Opalin.

OPALIN 3D structure. Source: alphafold

Opalin (OPALIN)

Gene Information

Human
Gene Name:	OPALIN
Uniprot:	Q96PE5
Entrez:	93377

Family

Belongs to:

No superfamily

Alternative Names

HTMP10transmembrane protein TMP10; oligodendrocytic myelin paranodal and inner loop proteinTMEM10; TMP10; Transmembrane protein 10opalin

Molecular Weight

Mass (kDA):
15.683 kDA

Genomic Context


Human

Location:	10q24.1
Sequence:	10; NC_000010.11 (96343216..96359365, complement)

Subcellular Localizations

Cell membrane; Single-pass type I membrane protein. In the CNS, enriched in the myelin paranodal and inner loop membranes, but not that of the PNS. Enriched in the leading edge of extending processes.

Diseases

Nervousness
Sclerosis
Aneurysm
Multiple Sclerosis
Encephalomyelitis
Demyelination
Experimental Autoimmune Encephalomyelitis
Epilepsy
Mycotic Aneurysm
Paraplegia
Autoimmune Reaction
Burkholderia Infections

Spastic Paraplegia
Fucosidase Deficiency Disease
Aneurysm, Infected
Leukemia
Inflammation
Injury Of Central Nervous System
Demyelinating Diseases

Pathways

Oligodendrocyte Differentiation
Myelination
Cell Migration
Myelin Assembly
Cell Death
Localization

PTMs

Deglycosylation

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

References

PMID: 11814680 by Nobile C., et al. Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia.