Recombinant Human Plexin A1 His-tag Protein, CF Summary
Additional Information |
Analyzed by SEC-MALS |
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Human Plexin A1 His-tag is immobilized at 2.50 µg/mL (100 µL/well), Recombinant Human Semaphorin 6C Fc Chimera
(Catalog #
2219-S6)
binds with an ED 50 of 1.00-6.00 μg/mL. |
Source |
Human embryonic kidney cell, HEK293-derived human Plexin A1 protein Glu27 - Pro1244, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Glu27 |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
135 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
130-150 kDa, under reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 6 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after opening.
- 3 months, -20 to -70 °C under sterile conditions after opening.
|
Buffer |
Supplied as a 0.2 μm filtered solution in PBS. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Plexin A1 His-tag Protein, CF
Background
Plexin A1, also known as Plexin 1, is a type I transmembrane protein
that is a member of the Plexin family of Semaphorin signal transducers (1). In humans,
the Plexin family consists of at least nine members divided into four
subfamilies and Plexin signaling is involved in neuronal axon guidance,
angiogenesis and immune response (2). Mature human Plexin A1 consists of an
extracellular domain (ECD) with one Sema domain, a spacer, and four tandem
IPT/TIG domains, a transmembrane segment, and a large cytoplasmic domain.
Within the ECD, human Plexin A1 shares 95% amino acid sequence identity with
mouse and rat Plexin A1. Plexin A1 binds Class 3 (secreted) Semaphorins
indirectly via Neuropilin (Npn)-1 and Npn-2 and binds
transmembrane Semaphorin 6D directly (3 ‑ 5). Sema3A engagement of
Plexin A1 and Npn-1 guides proprioceptive and sensory neurons during
development, while Sema3B engagement guides floorplate neurons (5-8).
In contrast, T cell Sema6D engagement of dendritic cell Plexin A1 controls
actin polymeration, which supports formation of immunological synapses and
enhances the function of the dendritic cells (3, 4, 9). Complex
formation with DAP12 allows Plexin A1 signaling through TREM family
proteins (10, 11). However, the most striking effect of
Plexin A1 deletion is on bone homeostasis, where Plexin A1-deficient mice
show increased trabecular bone mass due to downregulated osteoclast
differentiation (10). Plexin A1 and Sema6D are frequently expressed in
malignant pleural mesothelioma, where they promote anchorage-independent growth
through complexing with and activating VEGF R2 (12). Plexin A1 has also been
identified as a receptor for Slits and mediate commissural growth cone collapse
(13).
- Kameyama, T. et al. (1996) Biochem. Biophys. Res. Commun. 226:524.
- Kruger, R.P. et al. (2005) Nat. Rev. Mol. Cell Biol. 6:789.
- Takamatsu, H. et al. (2010) Cell. Mol. Immunol. 7:83.
- O’Connor, B.P. and J.P.Y. Ting (2008) Immunol. Res. 41:217.
- Takahashi, T. et al. (1999) Cell 99:59.
- Yoshida, Y. et al. (2006) Neuron 52:775.
- Toyofuku, T. et al. (2005) Nat. Neurosci. 8:1712.
- Nawabi, H. et al. (2010) Genes Dev. 24:396.
- Eun, S-Y. et al. (2006) J. Immunol. 177:4271.
- Takegahara, N. et al. (2006) Nat. Cell Biol. 8:615.
- Watarai, H. et al. (2008) Proc. Natl. Acad. Sci. USA 105:2993.
- Catalano, A. et al. (2009) Cancer Res. 69:1485.
- Delloye-Bourgeois, C. et al. (2015) Nat Neurosci 18:36.
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