Paired Box Protein Pax-6 (PAX6) Antibody

Este producto es parte de PAX - Paired box protein Pax
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559€ (100 µl)

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935106861
info@markelab.com
name
Paired Box Protein Pax-6 (PAX6) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx025233
tested applications
ELISA, WB, IF/ICC

Description

This gene encodes paired box gene 6, one of many human homologs of the Drosophila melanogaster gene prd. In addition to the hallmark feature of this gene family, a conserved paired box domain, the encoded protein also contains a homeo box domain. Both domains are known to bind DNA, and function as regulators of gene transcription. This gene is expressed in the developing nervous system, and in developing eyes. Mutations in this gene are known to cause ocular disorders such as aniridia and Peter's anomaly. Alternatively spliced transcript variants encoding either the same or different isoform have been found for this gene. [provided by RefSeq]. This antibody is supplied as crude ascites.

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Product specifications

CategoryPrimary Antibodies
Immunogen TargetPaired Box Protein Pax-6 (PAX6)
HostMouse
ReactivityHuman
Recommended DilutionWB: 1/500 - 1/16000, IF/ICC: 1/10 - 1/50. Optimal dilutions/concentrations should be determined by the end user.
ClonalityMonoclonal
ConjugationUnconjugated
IsotypeIgM Kappa
PurificationUnpurified crude ascites.
Size 1100 µl
FormLiquid
Tested ApplicationsELISA, WB, IF/ICC
BufferAscites containing 0.09% sodium azide.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDP26367
AliasAN,AN1,AN2,ASGD5,D11S812E,FVH1,MGDA,WAGR,Aniridia type II protein,Oculorhombin
BackgroundAntibody anti-PAX6
StatusRUO

Descripción

PAX6 is a highly conserved transcription factor critical for the development of the eyes, central nervous system, and endocrine pancreas. It regulates the expression of genes involved in eye morphogenesis, lens formation, and neuronal differentiation. PAX6 acts as a master regulator of ocular development, with its mutations causing congenital eye disorders such as aniridia, Peters anomaly, and microphthalmia. It also plays a role in brain patterning, where it contributes to neurogenesis and cortical layer formation. PAX6 is essential for pancreatic β-cell development, where it influences insulin production and glucose regulation. Dysregulation of PAX6 has been linked to neurological disorders and metabolic dysfunction. Knockout studies in mice reveal severe ocular malformations, brain developmental defects, and pancreatic abnormalities, highlighting its critical role in tissue differentiation, organogenesis, and cell fate determination during embryonic development.

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