R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
NOVA1 (E9E6U) Rabbit mAb #65350
Filter:
- WB
- IP
Supporting Data
REACTIVITY | H M R Mk |
SENSITIVITY | Endogenous |
MW (kDa) | 58 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
- M-Mouse
- R-Rat
- Mk-Monkey
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunoprecipitation | 1:100 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
NOVA1 (E9E6U) Rabbit mAb recognizes endogenous levels of total NOVA1 protein. This antibody does not cross-react with NOVA2 protein. This antibody detects an 85 kDa band of unknown origin.
Species Reactivity:
Human, Mouse, Rat, Monkey
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala36 of human NOVA1 protein.
Background
Neuro-oncological ventral antigen (NOVA) 1 and 2 are neuronal RNA-binding proteins (RBPs) that bind YCAY motifs to regulate alternative splicing (1-3). Both proteins have been shown to be targets in paraneoplastic opsoclonus myoclonus ataxia, a neuronal autoimmune disease (1,3). NOVA proteins rely on their KH3 domain to bind RNA and are reciprocally expressed in various parts of the brain (4). NOVA1 has been shown to be essential for neuronal viability, as it controls alternative splicing in GlyRalpha2 and GABA(A) receptor pre-mRNAs (5). NOVA1 is also capable of auto-regulation as it binds to its own exon 4, which contains a phosphorylated protein domain (6). NOVA1/2 double knockout mice are paralyzed due to lack of alternatively spliced agrin Z(+), which helps synapse formation at neuromuscular junctions (7). NOVA2 has been shown to regulate circular RNA biogenesis in the developing brain (8). NOVA1 has been shown to be highly expressed in many different cancer types, and can promote epithelial-mesenchymal transition by binding β-catenin mRNA (9,10).
- Buckanovich, R.J. et al. (1996) J Neurosci 16, 1114-22.
- Buckanovich, R.J. and Darnell, R.B. (1997) Mol Cell Biol 17, 3194-201.
- Yang, Y.Y. et al. (1998) Proc Natl Acad Sci U S A 95, 13254-9.
- Lewis, H.A. et al. (1999) Structure 7, 191-203.
- Dredge, B.K. et al. (2005) EMBO J 24, 1608-20.
- Ruggiu, M. et al. (2009) Proc Natl Acad Sci U S A 106, 3513-8.
- Cao, Y. et al. (2021) Mol Cell Biochem 476, 279-292.
- Knupp, D. et al. (2021) Nucleic Acids Res 49, 6849-6862.
- Liu, M. et al. (2020) Transl Cancer Res 9, 4373-4382.
- Tang, S. et al. (2020) RNA Biol 17, 881-891.
限制使用
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For Research Use Only. Not For Use In Diagnostic Procedures.
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