Recombinant Cyno/Rhesus L-Selectin/CD62L Fc Protein, CF
Recombinant Cyno/Rhesus L-Selectin/CD62L Fc Protein, CF Summary
Product Specifications
Recombinant Cyno/Rhesus L-Selectin (Trp52-Asn345) Accession # XP_005539996.1 | IEGRMD | Human IgG1 (Pro100-Lys330) |
N-terminus | C-terminus | |
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.
11192-LS
Formulation | Supplied as a 0.2 μm filtered solution in PBS with Trehalose. |
Shipping | The product is shipped with dry ice or equivalent. 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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Scientific Data
Recombinant Cynomolgus Monkey/Rhesus Macaque L‑Selectin/CD62L Fc Chimera Protein (Catalog # 11192-LS) supports the adhesion LS180 human colorectal adenocarcinoma cells. The ED50 for this effect is 0.300-3.60 μg/mL.
2 μg/lane of Recombinant Cynomolgus Monkey/Rhesus Macaque L‑Selectin/CD62L Fc Chimera Protein (Catalog # 11192-LS) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at 85-95 kDa and 170-190 kDa, respectively.
Reconstitution Calculator
Background: L-Selectin/CD62L
L-Selectin, also known as Leukocyte adhesion molecule 1 (LAM‑1) and CD62L, is a type-1 cell surface glycoprotein and cell adhesion molecule of the Selectin family (1). In humans, there are 3 Selectins, P, E, and L, and they are Ca2+ dependent lectins that help mediate the initial adhesive step during inflammation and immune surveillance (2). Mature L-Selectin consists of an extracellular domain (ECD) with a C-type lectin domain and an epidermal growth factor (EGF)-like domain, a transmembrane domain, and a short cytoplasmic domain. Within the ECD, cynomolgus L-Selectin shares 94% amino acid sequence identity with human L-Selectin. Several isoforms arising from alternative splicing have been reported, some with potential therapeutic implications (2,3). L-selectin is constitutively expressed on a wide variety of leukocytes and plays a role in the migration of lymphocytes into peripheral lymph nodes and sites of chronic inflammation, and of neutrophils into acute inflammatory sites (1-4). Acting in cooperation with P-Selectin and E-Selectin, L‑Selectin mediates the initial interaction of circulating leukocytes with endothelial cells that produces a characteristic "rolling" of the leukocytes on the endothelium (5). This initial interaction, also involving ICAM-1 and VCAM-1, leads eventually to extravasation of the white blood cell through the blood vessel wall into the extracellular matrix tissue (6). L-selectin function is required for normal Treg cell migration and over expression might be result in reduced tumor growth (7). A number of studies have reported that levels of L‑Selectin may be elevated or lowered in subjects with a variety of conditions, such as in Alzheimer's disease or rheumatoid arthritis (3, 5).
- Ivetic, A. et al. (2019) Front. Immunol. 10:1068.
- Grailer, J.J. et al. (2009) J. Dermatol sci. 56:141.
- Hirata, T. et al. (2015) Biochem Biophys Res. Commun. 462:371.
- Wedepohl, S. et al. (2012) Euro. J. Cell Biol. 91:257.
- Ivetic, A. et al. (2013) Inter. J. Biochem. Cell Biol. 45:550.
- Granger, D.N. and Senchenkova, E. (2010) Inflammation and the Microcirculation. San Rafael (CA): Morgan & Claypool Life Sciences Chapter 7.
- Watson, H.A. et al. (2019) Frontiers in immunology 10:1321.
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