Recombinant Human VCAM-1/CD106 His-tag Protein, CF Summary
Details of Functionality |
Measured by the ability of the immobilized protein to support the adhesion of U937 human histiocytic lymphoma cells. The ED50 for this effect is 0.5-3 μg/mL.
|
Source |
Chinese Hamster Ovary cell line, CHO-derived human VCAM-1/CD106 protein Phe25-Glu698, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Phe25 |
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 |
75 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 |
80-110 kDa, under reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 12 months from date of receipt, -20 to -70 °C as supplied.
- 2 weeks, 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 500 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 VCAM-1/CD106 His-tag Protein, CF
Background
VCAM-1, also known as CD106, is an
immunoglobulin (Ig)-like adhesion molecule that is mainly expressed in
endothelial cells and
other cell types including macrophages, dendritic cells, neurons, smooth muscle
cells, fibroblasts, and oocytes
(1, 2). It plays a critical role in inflammation by recruiting leukocytes
to acute and chronic inflammation sites (3, 4). Alternatively-spliced forms are
known to occur, but the most common form is a type I transmembrane protein with
a 674 aa extracellular domain (ECD) that includes seven C2-type immunoglobulin
domains, a 22 aa transmembrane segment, and a 19 amino acid (aa) cytoplasmic tail. Within the ECD, human VCAM-1 shares 75% and 76% aa
sequence identity with the mouse and rat VCAM-1, respectively. VCAM-1
binds to leukocyte integrins alpha 4 beta 1 (VLA-4) and alpha 4 beta 7. During
the inflammatory adhesion mechanism, activated integrins halt rolling
leukocytes and attach them firmly to the vascular endothelium. The
VCAM-1:VLA-4/ alpha 4 beta 7 interaction is also thought to be involved in the
extravasation of white blood cells through the blood vessel wall to sites of
inflammation (5). ELISA techniques have shown that detectable levels of soluble
VCAM-1 are present in the biological fluids of apparently normal individuals,
but elevated levels of serum VCAM-1 are indicative of future Atrial
Fibrillation incident as well as liver disease (6, 7). Tumor cells use
overexpression of VCAM-1 as means of escaping immune surveillance (8).
- Vonderheide, R.H. et al. (1994) J. Cell Biol. 125:215.
- Cybulsky, M.I. et al. (1991) Proc. Natl. Acad. Sci. USA 88:7859.
- Luster, A.D. et al. (2005) Nat. Immunol. 6:1182.
- Osborn, L. et al. (1989) Cell 59:1203
- Langer. H.F. et al. 2009. J Cell Mol Med. 13:1211.
- Willeit.K. et al. 2017. JAMA Cardiol. 2:516.
- Lo Iacono.O. et al. 2008. Liver Int. 28:1129.
- Wu.T.C. et al. 2007. Cancer Research. 67:6003
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