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MSX2 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | P35548 |
| Other Accession | Q03356, P70354, P52953, Q03358, P28362, Q0P5C3, P13297, P28360, P28361, O02786, P35993, P50223, NP_002440.2 |
| Reactivity | Human |
| Predicted | Chicken, Xenopus, Bovine, Mouse, Rat, Zebrafish |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 28897 Da |
| Antigen Region | 120-148 aa |
| Gene ID | 4488 |
|---|---|
| Other Names | Homeobox protein MSX-2, Homeobox protein Hox-8, MSX2, HOX8 |
| Target/Specificity | This MSX2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 120-148 amino acids from the Central region of human MSX2. |
| 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 | MSX2 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | MSX2 |
|---|---|
| Synonyms | HOX8 |
| Function | Acts as a transcriptional regulator in bone development. Represses the ALPL promoter activity and antagonizes the stimulatory effect of DLX5 on ALPL expression during osteoblast differentiation. Probable morphogenetic role. May play a role in limb-pattern formation. In osteoblasts, suppresses transcription driven by the osteocalcin FGF response element (OCFRE). Binds to the homeodomain-response element of the ALPL promoter. |
| Cellular Location | Nucleus. |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2.
References
Nikopensius, T., et al. Birth Defects Res. Part A Clin. Mol. Teratol. 88(9):748-756(2010)
Satoh, K., et al. J. Gastroenterol. 45(7):763-770(2010)
Doi, T., et al. J. Pediatr. Surg. 45(6):1187-1191(2010)
Jagomagi, T., et al. Eur. J. Oral Sci. 118(3):213-220(2010)
Jugessur, A., et al. PLoS ONE 5 (7), E11493 (2010) :
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