Pax6 Antibody (PAX6/1166) [Phycoerythrin] Summary
| Immunogen |
Recombinant fragment (N-terminus; aa 1-300) of human PAX6 protein
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| Localization |
Nuclear
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| Marker |
Stem Cell Marker
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| Specificity |
Pax genes contain paired domains with strong homology to genes in Drosophila, which are involved in programming early development. Lesions in the Pax-6 gene account for most cases of aniridia, a congenital malformation of the eye, chiefly characterized by iris hypoplasia, which can cause blindness. Pax-6 is involved in other anterior segment malformations besides aniridia, such as Peters anomaly, a major error in the embryonic development of the eye with corneal clouding with variable iridolenticulocorneal adhesions. The Pax-6 gene encodes a transcriptional regulator that recognizes target genes through its paired-type DNA-binding domain. The paired domain is composed of two distinct DNA-binding subdomains, the amino-terminal subdomain and the carboxy-terminal subdomain, which bind respective consensus DNA sequences. The human Pax-6 gene produces two alternatively spliced isoforms that have the distinct structure of the paired domain.
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| Isotype |
IgG1 Kappa
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| Clonality |
Monoclonal
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| Host |
Mouse
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| Gene |
PAX6
|
| Purity |
Protein A or G purified
|
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Applications/Dilutions
| Dilutions |
|
| Application Notes |
Optimal dilution of this antibody shomld be experimentally determined.
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Packaging, Storage & Formulations
| Storage |
Store at 4C in the dark.
|
| Buffer |
PBS
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| Preservative |
0.05% Sodium Azide
|
| Purity |
Protein A or G purified
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Alternate Names for Pax6 Antibody (PAX6/1166) [Phycoerythrin]
- keratitis)
- MGC17209
- Oculorhombin
- paired box 6
- paired box protein Pax-6
- Pax6