Mouse Artemin Antibody Summary
Ala112-Gly224
Accession # Q9Z0L2.1
Applications
under non-reducing conditions only
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: Artemin
Artemin is a member of the Glia Cell-Derived Neurotrophic factor (GDNF) family ligands, which include GDNF, Persephin, Artemin, and Neurturin. GDNF family ligands are distant members of the Transforming Growth Factor beta (TGF‑ beta ) superfamily (1‑4). Similar to other TGF‑ beta family proteins, Artemin is synthesized as a large precursor protein that is cleaved at the dibasic cleavage site (RXXR) to release the carboxy-terminal domain. The carboxy-terminal domain of Artemin contains the characteristic seven conserved cysteine residues necessary for the formation of the cysteine-knot and the single interchain disulfide bond. Biologically active Artemin is a disulfide‑linked homodimer of the carboxy-terminal 113 amino acid residues. Mature mouse Artemin shares 88.5% amino acid sequence similarity with human Artemin. Mature Artemin also shares approximately 40% amino acid sequence identity with the other three members of the GDNF family ligands (5). Bioactivities of all GDNF family ligands are mediated through a receptor complex composed of a high affinity ligand binding component (GFR alpha 1‑GFR alpha 4) and a common signaling component, cRET (receptor tyrosine kinase) (5‑8). Artemin prefers to bind to GFR alpha 3 and activites the GFR alpha 3‑RET. However, in the presence of RET, it can bind to GFR alpha 1 as well (4, 5, 9). Artemin has been shown to promote the survival and growth of various peripheral and central neurons, including sympathetic and dopaminergic neurons. It may also play an important role in the development of sympathetic neurons and several organs (5, 10, 11).
- Lin, L-F.H. et al. (1993) Science 260:1130.
- Milbrandt, J. et al. (1998) Neuron 20:245.
- Kotzbauer, P.T. et al. (1996) Nature 384:467.
- Baloh, R.H. et al. (1998) Neuron 21:1291.
- Takahashi, M. (2001) Cytokine and Growth Factor Reviews 12:361.
- Baloh, R.H. et al. (1997) Neuron 18:793.
- Jing, S. et al. (1996) Cell 85:1113.
- Jing, S. et al. (1997) J Biol Chem 272:33111.
- Nishino, J. et al. (1999) Neuron 23:725.
- Enomoto, H. et al. (2001) Development 128:3963.
- Andres, R. et al. (2001) Development 128:3685.
Product Datasheets
Citations for Mouse Artemin Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Immunoglobulin somatic hypermutation in a defined biochemical system recapitulates affinity maturation and permits antibody optimization
Authors: SL Jeong, H Zhang, S Yamaki, C Yang, DD McKemy, MR Lieber, P Pham, MF Goodman
Nucleic Acids Research, 2022-11-11;0(0):.
Species: Mouse
Sample Types: In Vivo
Applications: In Vivo -
Inflammatory and neuropathic cold allodynia are selectively mediated by the neurotrophic factor receptor GFR?3
Authors: EK Lippoldt, S Ongun, GK Kusaka, DD McKemy
Proc Natl Acad Sci USA, 2016-04-05;113(16):4506-11.
Species: Mouse
Sample Types: In Vivo
Applications: Neutralization -
Artemin-GFRalpha3 interactions partially contribute to acute inflammatory hypersensitivity.
Authors: Thornton P, Hatcher J, Robinson I, Sargent B, Franzen B, Martino G, Kitching L, Glover C, Anderson D, Forsmo-Bruce H, Low C, Cusdin F, Dosanjh B, Williams W, Steffen A, Thompson S, Eklund M, Lloyd C, Chessell I, Hughes J
Neurosci Lett, 2013-04-19;545(0):23-8.
Species: Mouse
Sample Types: Plasma
Applications: Neutralization
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