VAX1 Antibodies

AND VAX1 ELISA kits, VAX1 Proteins

Many biological assays use antibodies to detect VAX1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with VAX1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop VAX1 antibodies...

We validate the specificity of these antibodies to VAX1 by testing them on tissues known to express VAX1 positively and negatively. Browse below to find the VAX1 antibody that suites your experiment. We have 4 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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VAX1 Infographic by Boster Bio

All VAX1 Products

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Specificity

Applications

Price

Anti-Ventral anterior homeobox 1 VAX1 Antibody

Human, Mouse, Rat

ELISA, WB

$380
Cat # A09523
100ul

VAX1 (NM_199131) Human Recombinant Protein

$813
Cat # PROTQ5SQQ9
20 µg

Anti-VAX1 Mouse Monoclonal Antibody [Clone ID: OTI1E6]

Human, Mouse, Rat

IHC, WB

$523
Cat # M09523-1
100 µl

Anti-VAX1 Mouse Monoclonal Antibody [Clone ID: OTI4E5]

Human, Mouse, Rat

IHC, WB

$523
Cat # M09523
100 µl

VAX1 Overview

Facts about Ventral anterior homeobox 1.

VAX1 3D structure. Source: alphafold

Ventral anterior homeobox 1 (VAX1)

Transcription factor that may function in dorsoventral specification of the forebrain. Required for axon guidance and major tract formation in the developing forebrain.

May contribute to the differentiation of the neuroretina, pigmented epithelium and optic stalk (By similarity). .

Gene Information

Human
Gene Name:	VAX1
Uniprot:	Q5SQQ9
Entrez:	11023

Family

Belongs to:

EMX homeobox family

Alternative Names

MGC126743; MGC126745; ventral anterior homeobox 1

Molecular Weight

Mass (kDA):
34.713 kDA

Genomic Context


Human

Location:	10q25.3
Sequence:	10; NC_000010.11 (117128520..117138270, complement)

Subcellular Localizations

Nucleus.

Diseases

Congenital Ocular Coloboma (disorder)
Congenital Absence
Dysplasia
Cleft Palate
Agenesis Of Corpus Callosum
Microphthalmos
Eye Abnormalities
Malignant Neoplasms
Cleft Lip
Congenital Abnormality
Holoprosencephaly
Septo-optic Dysplasia
Stage, Carcinoma Of Unknown Primary

Retinal Degeneration
Anophthalmos
Craniofacial Abnormalities
Malignant Neoplasm Of Lung
Malignant Neoplasm Of Urinary Bladder
Carcinoma
Fundus Coloboma

Pathways

Eye Development
Cell Proliferation
Dna Methylation
Localization
Methylation
Cell Differentiation
Neural Tube Closure
Cell Migration
Dna Hypermethylation
Neurogenesis
Optic Vesicle Morphogenesis
Neuroblast Proliferation
Eye Morphogenesis

Tube Closure
Axon Guidance
Cell Death
Forebrain Development
Corpus Callosum Development
Regionalization
Pathogenesis

PTMs

Methylation

Research Areas

Vision

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/VAX1

References

PMID: 22095910 by Slavotinek A.M., et al. VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans.