Netrin-3 Antibodies

AND NTN3 ELISA kits, Netrin-3 Proteins

Many biological assays use antibodies to detect Netrin-3, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Netrin-3 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Netrin-3 antibodies...

We validate the specificity of these antibodies to Netrin-3 by testing them on tissues known to express NTN3 positively and negatively. Browse below to find the NTN3 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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NTN3 Infographic by Boster Bio

All NTN3 Products

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Product

Figures

Specificity

Applications

Price

NTN3 (NM_006181) Human Over-expression Lysate

Human

$960
Cat # LS004917
100 µg

Anti-NTN3 Antibody Picoband®

Human, Rat

ELISA, IF, IHC, ICC, WB

$370
Cat # A17692
100 µg/vial

NTN3 Overview

Facts about Netrin-3.

Netrin-3 (NTN3)

Netrins control guidance of CNS commissural axons and peripheral motor axons. .

Gene Information

Human
Gene Name:	NTN3
Uniprot:	O00634
Entrez:	4917

Family

Belongs to:

No superfamily

Alternative Names

Netrin2; Netrin-2

Molecular Weight

Mass (kDA):
61.466 kDA

Genomic Context


Human

Location:	16p13.3
Sequence:	16; NC_000016.10 (2471297..2474145)

Subcellular Localizations

Secreted, extracellular space, extracellular matrix.

Diseases

Congenital Disorders
Hereditary Diseases
Hirschsprung Disease
Cytogenetic Abnormality

Interacting Proteins

DRAXIN

Pathways

Pathogenesis

PTMs

Disulfide bond

Glycoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NTN3

References

PMID: 8828041 by Burn T.C., et al. Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3.

PMID: 9143507 by Van Raay T.J., et al. The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3.