Homeobox protein aristaless-like 3 (ALX3) Antibody (Biotin)

Este producto es parte de ALX - ALX Homeobox
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260€ (50 µl)

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935106861
info@markelab.com
name
Homeobox protein aristaless-like 3 (ALX3) Antibody (Biotin)
category
Primary Antibodies
provider
Abbexa
reference
abx341240
tested applications
ELISA

Description

Homeobox protein aristaless-like 3 (ALX3) Antibody (Biotin) is a Rabbit Polyclonal antibody conjugated to Biotin for the detection of Human ALX3.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetHomeobox protein aristaless-like 3 (ALX3)
HostRabbit
ReactivityHuman
Recommended DilutionOptimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationBiotin
IsotypeIgG
Purity> 95%
PurificationPurified by Protein G chromatography.
Size 150 µl
Size 2100 µl
Size 3200 µl
Size 41 ml
FormLiquid
Tested ApplicationsELISA
Buffer0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% glycerol.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDO95076
Gene ID257
OMIM136760
AliasFND,FND1
BackgroundAntibody anti-ALX3
StatusRUO

Descripción

ALX3 is a transcription factor belonging to the homeobox gene family, which regulates developmental processes, including craniofacial development, limb formation, and neural crest cell differentiation. ALX3 is expressed in facial mesenchymal tissues during embryogenesis, where it controls genes necessary for midline and upper facial development. Mutations or dysregulation of ALX3 are linked to frontonasal dysplasia, characterized by cleft lip/palate, hypertelorism, and nasal malformations. ALX3 has been shown to interact with other transcription factors and signaling pathways to regulate the proliferation and migration of mesenchymal cells. Emerging studies suggest ALX3 may act as a tumor suppressor in certain cancers, as its expression has been shown to inhibit cell proliferation and epithelial-mesenchymal transition (EMT). Its role in regulating gene expression during development and disease highlights ALX3 as a potential target for understanding congenital malformations and tumorigenesis.

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