Recombinant Human Neurexophilin-1/NXPH1 Protein, CF
Recombinant Human Neurexophilin-1/NXPH1 Protein, CF Summary
Product Specifications
Ala22-Gly271, with a C-terminal 6-His tag
Analysis
Product Datasheets
Carrier Free
CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.
In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.
4957-NX
Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
Reconstitution | Reconstitute at 100 μg/mL in sterile PBS. |
Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
Stability & Storage: | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Reconstitution Calculator
Background: Neurexophilin-1
Neurexophilin-1 (NXPH1) is one of at least four vertebrate neuropeptide-like secreted glycoproteins in the neurexophilin family (1, 2). The 271 amino acid (aa) NXPH1 sequence contains a 21 aa signal peptide, an 86 aa propeptide that is cleaved at a basic motif, and a 164 aa mature protein that contains three potential N-glycosylation sites in the N-terminal portion and six conserved cysteines in the C-terminal portion (1). Mature human NXPH1 shares 99% aa identity with mouse, rat, equine, bovine and canine NXPH1. NXPH1 is expressed selectively in subpopulations of neurons within the cerebral cortex, cerebellum and olfactory bulb that are thought to be inhibitory interneurons (2, 3). In humans, NXPH-2 and -3 are most similar to NXPH1, sharing 84% and 64% aa identity within the mature region, respectively. In rodents, which do not express NXPH-2, expression of NXPH1 and NXPH-3 does not appear to coincide. However, both serve as tightly bound extracellular ligands for alpha -neurexins, synaptic transmembrane molecules that are essential for calcium-triggered neurotransmitter release (1, 4, 5). By contrast, NXPH-4 does not bind alpha -neurexins (1, 4). Genetic deletion of NXPH1 and/or NXPH-3 produces no anatomical effect, although mice lacking NXPH-3 show defects in motor coordination (4, 6).
- Missler, M. et al. (1998) J. Neurosci. 18:3630.
- Petrenko, A. G. et al. (1996) J. Neurosci. 16:4360.
- Clarris, H. J. et al. (2002) Int. J. Dev. Biol. 46:649.
- Missler, M. et al. (1998) J. Biol. Chem. 273:34716.
- Dudanova, I. et al. (2006) J. Neurosci. 26:10599.
- Beglopoulos, V. et al. (2005) Mol. Cell. Biol. 25:7278.
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