ODAPH Antibodies

AND ODAPH ELISA kits, ODAPH Proteins

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

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

All ODAPH Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

ODAPH (NM_178497) Human Recombinant Protein

$1249
Cat # PROTQ17RF5
20 µg

ODAPH (NM_178497) Human Over-expression Lysate

Human

$628
Cat # LS152816
100 µg

Anti-ODAPH Antibody Picoband®

Human

ELISA, WB

$370
Cat # A32235-1
100 µg/vial

ODAPH Overview

Facts about Odontogenesis associated phosphoprotein.

ODAPH 3D structure. Source: alphafold

Odontogenesis associated phosphoprotein (ODAPH)

May promote nucleation of hydroxyapatite. .

Gene Information

Human
Gene Name:	ODAPH
Uniprot:	Q17RF5
Entrez:	152816

Family

Belongs to:

No superfamily

Alternative Names

Odontogenesis associated phosphoprotein

Molecular Weight

Mass (kDA):
15.556 kDA

Genomic Context


Human

Location:	4q21.1
Sequence:	4; NC_000004.12 (75554997..75565893)

Tissue Specificity

Highly expressed in placenta.

Subcellular Localizations

Secreted.

Diseases

Amelogenesis imperfecta, hypomaturation type, 2A4 (AI2A4)

Interacting Proteins

MDFI

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

References

PMID: 22901946 by Parry D.A., et al. Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.

PMID: 27558265 by Prasad M.K., et al. Amelogenesis Imperfecta: 1 family, 2 phenotypes, and 2 mutated Genes.