PAX9 Antibody (N-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
---|---|
Primary Accession | P55771 |
Other Accession | Q2L4T2, P47242, P55166, NP_006185.1, Q98866 |
Reactivity | Human |
Predicted | Zebrafish, Chicken, Mouse, Rat |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 36310 Da |
Antigen Region | 69-95 aa |
Gene ID | 5083 |
---|---|
Other Names | Paired box protein Pax-9, PAX9 |
Target/Specificity | This PAX9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 69-95 amino acids from the N-terminal region of human PAX9. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | PAX9 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | PAX9 |
---|---|
Function | Transcription factor required for normal development of thymus, parathyroid glands, ultimobranchial bodies, teeth, skeletal elements of skull and larynx as well as distal limbs. |
Cellular Location | Nucleus. |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene is a member of the paired box (PAX) family of transcription factors. Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes play critical roles during fetal development and cancer growth. The specific function of the paired box 9 gene is unknown but it may involve development of stratified squamous epithelia as well as various organs and skeletal elements.
References
Pawlowska, E., et al. Orthod Craniofac Res 13(3):142-152(2010) Mostowska, A., et al. Birth Defects Res. Part A Clin. Mol. Teratol. 88(7):538-545(2010) Haldeman-Englert, C.R., et al. J Craniofac Surg 21(3):837-839(2010) Jugessur, A., et al. PLoS ONE 5 (7), E11493 (2010) : Mues, G., et al. J Craniofac Surg 20 SUPPL 2, 1652-1654 (2009) :
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