ALX3 Antibodies

AND ALX3 ELISA kits, ALX3 Proteins

Many biological assays use antibodies to detect ALX3, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with ALX3 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop ALX3 antibodies...

We validate the specificity of these antibodies to ALX3 by testing them on tissues known to express ALX3 positively and negatively. Browse below to find the ALX3 antibody that suites your experiment. We have 5 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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ALX3 Infographic by Boster Bio

All ALX3 Products

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Product

Figures

Specificity

Applications

Price

Anti-ALX3 Antibody

6 Q&As

Human, Mouse, Rat

IF, WB

$360
Cat # A10111
100 µl

ALX3 Colorimetric Cell-Based ELISA

Human, Mouse, Rat

ELISA

$480
Cat # EKC1657
1 kit, containing one 96-well plate and all necessary reagents

Anti-ALX3 (R203) Antibody

Human, Mouse, Rat

IF, IHC, WB

$405
Cat # A10111-1
100ul

ALX3 (NM_006492) Human Recombinant Protein

$1249
Cat # PROTO95076
20 µg

ALX3 (NM_006492) Human Over-expression Lysate

Human

$628
Cat # LS000257
100 µg

ALX3 Overview

Facts about Homeobox protein aristaless-like 3.

ALX3 3D structure. Source: alphafold

Homeobox protein aristaless-like 3 (ALX3)

Transcriptional regulator with a possible role in patterning of mesoderm during development. .

Gene Information

Human
Gene Name:	ALX3
Uniprot:	O95076
Entrez:	257

Family

Belongs to:

paired homeobox family

Alternative Names

ALX homeobox 3; aristaless-like homeobox 3; homeobox protein aristaless-like 3; MGC138212; MGC141988; Proline-rich transcription factor ALX3

Molecular Weight

Mass (kDA):
36.935 kDA

Genomic Context


Human

Location:	1p13.3
Sequence:	1; NC_000001.11 (110059870..110070672, complement)

Subcellular Localizations

Nucleus.

Diseases

Congenital Abnormality
Craniofacial Abnormalities
Polydactyly
Frontonasal Dysplasia
Dysplasia
Malignant Neoplasms
Neoplasms
Diabetes Mellitus
Orbital Separation Excessive
Insulin Resistance
Cleft Lip
Crest Syndrome

Adenoma
Microphthalmos
Non-neoplastic Disorder
Hypoplasia Of Scrotum
Sarcoma
Congenital Cerebral Hernia
Congenital Anomaly Of Face

Pathways

Methylation
Neural Tube Closure
Dna Hypermethylation
Limb Development
Glucose Homeostasis
Tube Closure
Transport
Cell Proliferation
Insulin Secretion
Dna Methylation
Regulation Of Glucose Homeostasis
Tissue Development

Translation
Cell Death
Interphase
Pathogenesis
Oncogenesis
Secretion

PTMs

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ALX3

References

PMID: 11807986 by Wimmer K., et al. Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma.

PMID: 19409524 by Twigg S.R.F., et al. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.