Recombinant Human Integrin alpha 2 beta 1 Protein, CF Summary
Details of Functionality
Measured by its binding ability in a functional ELISA. When bovine collagen-II is coated at 10 μg/mL, Recombinant Human Integrin alpha 2 beta 1 binds with an apparent Kd <1nM.
Source
Chinese Hamster Ovary cell line, CHO-derived human Integrin alpha 2 beta 1 protein
Human Integrin alpha 2 (Tyr30-Thr1132) Accession # NP_002194
HPGGGSGGGS
Human c-Jun (Arg276-His315)
Human Integrin beta 1 (Gln21-Asp728) Accession # P05556
>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
Binding Activity
Theoretical MW
126 kDa ( alpha 2) & 83.3 kDa ( beta 1). 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.
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 200 μg/mL in PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Integrin alpha 2 beta 1 Protein, CF
alpha 2 integrin
alpha 2 subunit of VLA-2 receptor
BR
CD49 antigen-like family member B
CD49b
collagen receptor
glycoprotein Ia
GPIa
HPA-5
human platelet alloantigen 5
human platelet alloantigen system 5
Integrin alpha 2 beta 1
integrin alpha-2
integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
platelet antigen Br
platelet glycoprotein GPIa
platelet membrane glycoprotein Ia
very late activation protein 2 receptor, alpha-2 subunit
very late activation receptor alpha-2 subunit
very late activation receptor subunit alpha-2
VLA-2
VLAA2
Background
Integrin alpha 2 beta 1 is one of twelve integrin family adhesion receptors that share the beta 1 subunit (1-3). It is the non-covalent heterodimer of 160 kDa alpha 2 (CD49b) and 130 kDa beta 1 (CD29) type I transmembrane glycoprotein subunits and is one of six very late antigens on activated T cells, designated VLA2 (3). The alpha 2 extracellular domain (ECD) contains an I (inserted) domain which includes the ligand binding site (2, 3). The beta 1 ECD contains a vWFA domain, which participates in binding. Each subunit then has a transmembrane sequence and a short cytoplasmic tail. The dimer is folded when it is least active. Divalent cations and intracellular (inside-out) signaling convert it to its most active, extended and open conformation (1, 2). The 1102 amino acid (aa) human alpha 2 extracellular domain (ECD) shares 83-89% aa sequence identity with mouse, rat, canine, bovine and equine alpha 2, while the 708 aa human beta 1 ECD shares 92-96% aa sequence identity with rat, bovine, mouse, and feline beta 1. The I domain-containing beta 1 integrins ( alpha 1 beta 1, alpha 2 beta 1, alpha 10 beta 1 and alpha 11 beta 1) all bind collagens, with alpha 2 beta 1 preferring collagens I-III (4, 5). Platelet alpha 2 beta 1, also called GPIa, cooperates with another adhesion protein, GPVI, to coordinate platelet collagen binding and activation (3, 6, 7). Other alpha 2 beta 1 ligands include laminin, decorin, E‑cadherin, and collagen-like regions of collectin molecules such as C1q (4). Adhesion is synergized by crosstalk with syndecan-1 or HGF R/c-Met, and antagonized by crosstalk with Integrin alpha 1 beta 1 (8-10). In addition to expression on selected hematopoietic cells, alpha 2 beta 1 is present on a wide variety of non‑hematopoietic cells (4). Mice deficient in the alpha 2 subunit have defects in innate immune responses, wound mast cell infiltration and angiogenesis, and platelet responses to collagen (6, 11, 12). In innate immunity, alpha 2 beta 1 binding to C1q initiates the complement cascade and costimulates mast cell activation, triggering neutrophil influx (4, 12).
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McCall-Culbreath, K.D. et al. (2008) Blood 111:3562.
Abair, T.D. et al. (2008) Exp. Cell Res. 314:3593.
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